Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-23T23:03:33.812Z Has data issue: false hasContentIssue false

Adverse childhood experiences and adult diet quality

Published online by Cambridge University Press:  29 October 2021

Sydney R. Aquilina
Affiliation:
Trinity College of Arts & Sciences, Duke University, Durham, NC, USA
Martha J. Shrubsole
Affiliation:
Division of Epidemiology, Department of Medicine, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN, USA
Julia Butt
Affiliation:
Infections and Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany
Maureen Sanderson
Affiliation:
Department of Family and Community Medicine, Meharry Medical College, Nashville, TN, USA
David G. Schlundt
Affiliation:
Department of Psychology, Vanderbilt University, Nashville, TN, USA
Mekeila C. Cook
Affiliation:
Division of Public Health Practice, Meharry Medical College, Nashville, TN, USA
Meira Epplein*
Affiliation:
Department of Population Health Sciences, Duke University and Cancer Risk, Detection, and Interception Program, Duke Cancer Institute, Durham, NC, USA
*
*Corresponding author: Meira Epplein, email [email protected]

Abstract

Childhood trauma is strongly associated with poor health outcomes. Although many studies have found associations between adverse childhood experiences (ACEs), a well-established indicator of childhood trauma and diet-related health outcomes, few have explored the relationship between ACEs and diet quality, despite growing literature in epidemiology and neurobiology suggesting that childhood trauma has an important but poorly understood relationship with diet. Thus, we performed a cross-sectional study of the association of ACEs and adult diet quality in the Southern Community Cohort Study, a largely low-income and racially diverse population in the southeastern United States. We used ordinal logistic regression to estimate the association of ACEs with the Healthy Eating Index-2010 (HEI-10) score among 30 854 adults aged 40–79 enrolled from 2002 to 2009. Having experienced any ACE was associated with higher odds of worse HEI-10 among all (odds ratio (OR) 1⋅22; 95 % confidence interval (CI) 1⋅17, 1⋅27), and for all race–sex groups, and remained significant after adjustment for adult income. The increasing number of ACEs was also associated with increasing odds of a worse HEI-10 (OR for 4+ ACEs: 1⋅34; 95 % CI 1⋅27, 1⋅42). The association with worse HEI-10 score was especially strong for ACEs in the household dysfunction category, including having a family member in prison (OR 1⋅34; 95 % CI 1⋅25, 1⋅42) and parents divorced (OR 1⋅25; 95 % CI 1⋅20, 1⋅31). In summary, ACEs are associated with poor adult diet quality, independent of race, sex and adult income. Research is needed to explore whether trauma intervention strategies can impact adult diet quality.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society

Introduction

Adverse childhood experiences (ACEs) include a wide breadth of exposures related to abuse, household dysfunction and neglect. In the original ACE study by CDC-Kaiser, these exposures were assessed in two waves through an extensive multipart health questionnaire totalling sixty-eight questions in the final wave(Reference Felitti, Anda and Nordenberg1). Subsequent studies have condensed the original questionnaire into ten questions, representing: emotional abuse; physical abuse; sexual abuse; emotional neglect; physical neglect; parents divorced; mother abused; live with alcohol or drug use; live with depression or suicide and family member in prison(Reference Felitti, Anda and Nordenberg1Reference Martin-Higarza, Fontanil and Mendez4).

ACEs are now understood to be both common, affecting approximately two-thirds of the general population, and pervasive, increasing risk of many unhealthy behaviours and chronic diseases(Reference Felitti, Anda and Nordenberg1,Reference Windle, Dehghani and Roy5Reference Amemiya, Fujiwara and Shirai7) . For instance, people with four or more ACEs were twice as likely to smoke, seven times more likely to be an alcoholic and twelve times more likely to have attempted suicide in comparison to those with three or fewer ACEs in the original ACE study. ACEs were associated with many chronic health conditions including asthma, cardiovascular disease, diabetes and cancer(Reference Felitti, Anda and Nordenberg1,Reference Waehrer, Miller and Silverio Marques8) . In addition, studies suggest that the effects of ACEs are cumulative. For example, a study by Merrick et al. found ACEs to have a cumulative effect (across 1, 2–3 and 4+ ACEs) on the odds of chronic conditions, depression, health risk behaviours (smoking, heavy drinking) and socioeconomic challenges(Reference Merrick, Ford and Ports9). Among racial minorities and individuals with lower socioeconomic status (SES), associations have been found to be even stronger(Reference Deschenes, Graham and Kivimaki10Reference Mersky, Topitzes and Reynolds13).

The Healthy Eating Index-2010 (HEI-10) is a valid and reliable measure of diet quality developed by the United States Department of Agriculture (USDA) and U.S. Department of Health and Human Services (HHS) to reflect the Dietary Guidelines for Americans(Reference Guenther, Casavale and Reedy14,Reference Guenther, Kirkpatrick and Reedy15) . However, neither the HEI-10 nor any comprehensive food frequency questionnaire (FFQ) has been used to evaluate the impact of ACEs on adult diet, despite growing literature in epidemiology and neurobiology suggesting that childhood trauma has an important but poorly understood relationship with diet(Reference Anda, Felitti and Bremner16).

For instance, associations have been found between ACEs and many diet-related conditions such as obesity, binge-eating disorder, food addiction, irritable bowel syndrome, inflammatory bowel disease, bulimia nervosa, anorexia nervosa, elevated cortisol levels, pro-inflammatory gut microbiota and more general dysregulation of the immune and endocrine systems(Reference Coffino, Grilo and Udo17Reference Witges, Bernstein and Sexton27). Additionally, a recent study by Schuler et al. found cumulative and individual ACEs to predict poor diet quality among children(Reference Schuler, Vazquez and Kobulsky28). By establishing evidence of an association of ACEs with poor diet quality in childhood, Schuler et al.'s findings also suggest the possibility of ACE-induced poor diet quality in adulthood through a continuation of poor childhood diet. Given the complexity of the impact of childhood trauma on both brain structure (e.g. size of prefrontal cortex) and function (e.g. dysregulation of the hypothalamic–pituitary–adrenal (HPA) axis), the multi-system involvement of these variables within the human body, and the contextual importance of environmental factors for any such variables or systems, there are many pathways which could potentially result in an ACE–adult diet quality (as represented by the HEI-10) association(Reference Dempster, O'Leary and MacNeil19,Reference Baskind, Taveras and Gerber29Reference Miguel, Pereira and Silveira34) .

In the present study, we sought to evaluate the association of ACEs and adult diet quality assessed using an FFQ in the Southern Community Cohort Study (SCCS), a prospective study of approximately 85 000 adults over age 40 in the southeastern United States established to study cancer and other health outcomes, particularly in underserved populations(Reference Signorello, Hargreaves and Blot35). Previously, studies of SCCS participants have found ACEs to be associated with adult cancer risk behaviours, greater chronic disease burden and higher adult health care utilisation. These studies also suggest that there may be race and sex differences for ACEs that have not been well explored(Reference Hargreaves, Mouton and Liu36,Reference Mouton, Hargreaves and Liu37) . Another study conducted in the SCCS used the HEI-10, finding better diet quality to be associated with a lower risk of death for all-cause mortality(Reference Yu, Sonderman and Buchowski38). These results suggest that the HEI-10 derived from an FFQ is a good proxy for diet quality in this population.

Ultimately, the present study aims to broaden our understanding of the associations of childhood trauma and adult health. More specifically, the present study explores whether having traumatic experiences during childhood significantly increases odds of poor diet as an adult, and whether these associations differ by race or sex, among participants of the SCCS. Our a priori hypothesis is that ACEs are associated with lower quality of adult diet, and that this association might be particularly impactful among racially marginalised communities.

Methods

Study design and participants

Data were collected from the SCCS, a multi-year prospective cohort of approximately 85 000 adults from 12 southeastern states in the US enrolled between ages 40–79 in the years 2002–9, primarily from community health clinics that serve the under- and uninsured(Reference Signorello, Hargreaves and Blot35). We included participants who (1) completed the FFQ from the baseline at enrolment, such that HEI-10 could be calculated and (2) completed the ACE survey from the second follow-up questionnaire administered in 2012(Reference Signorello, Hargreaves and Blot35).

Of the 84 508 total current SCCS participants, those with insufficient completion of the FFQ (>10 food items left blank) and implausible energy intakes (<600 or >8000 kcal/d) were excluded (n 6042). Additionally, since numbers were small for racial groups other than Black or White (n 4123), we did not include them in the present analysis. Of these 74 343, 36 569 completed the second follow-up questionnaire, and were more likely to be older, female, white and have higher SES compared with the total population, while still generally reflecting the overall low SES SCCS population. Of these participants who returned for the second follow-up, 84⋅4 % completed the ACE questionnaire in full, such that only 15⋅6 % (n 5715) were excluded because they were missing at least one of the ACE questions. Thus, we performed a retrospective cohort analysis including a total of 30 854 SCCS participants (18 769 Blacks; 12 085 Whites). Analyses were conducted by self-reported sex and race among all and in the following groups: Black females (n 12 576); Black males (n 6193); White females (n 7704); White males (n 4381). Importantly, the relationship between ACEs and adult HEI-10 can be assumed to be temporal, as ACEs are acquired during childhood and adult HEI-10 was the outcome measured. Due to the high cost of a healthy diet, which could have a disproportionate impact on the population by ACE score, we secondarily included adult household income as a variable in the model to estimate the ACE-HEI association above and beyond the association with income level.

Study instruments and assessment of variables

The original ACE questionnaire described earlier has been well validated as a reliable measure of childhood trauma(Reference Felitti, Anda and Nordenberg1Reference Martin-Higarza, Fontanil and Mendez4). The usage of condensed versions has also been found to be valid and reliable(Reference Dube, Williamson and Thompson39,Reference Wade, Becker and Bevans40) . Thus, a modified version of the original ACE questionnaire was used in the present study with only ten questions, each reflecting one of the ten identified ACEs of emotional abuse, physical abuse, sexual abuse, emotional neglect, physical neglect, parents divorced, mother physically abused, lived with an alcohol or drug abuser, had a household member who was mentally ill or attempted suicide, and had a household member go to prison. Results from this abbreviated ACE questionnaire have been found to be associated with adult cancer risk behaviours and health care utilisation in the SCCS population(Reference Hargreaves, Mouton and Liu36,Reference Mouton, Hargreaves and Liu37) .

The FFQ created and utilised by the SCCS (as previously described(Reference Buchowski, Schlundt and Hargreaves41)) was empirically designed to account for race and geographic region using the National Health and Nutrition Examination Survey (NHANES) and Continuing Survey of Food Intakes by Individuals (CSFII) 24-hour recall databases(Reference Signorello, Munro and Buchowski42). From the resulting FFQ variables, the HEI-10 score was calculated(Reference Yu, Sonderman and Buchowski38). As discussed earlier, the HEI-10 is a valid and reliable measure of diet quality developed by the USDA and HHS to reflect the Dietary Guidelines for Americans(Reference Guenther, Casavale and Reedy14,Reference Guenther, Kirkpatrick and Reedy15) . There are twelve components included in the HEI-10 score (scaled from 0 to 100), which are added together for the total HEI-10 score, and included: total fruit, whole fruit, whole grains, total dairy products, total vegetables, greens and beans, total protein foods, seafood and plant proteins, fatty acids, sodium, solid fat/alcohol/added sugar and refined grains. Depending on the component, scoring is based on adequacy or moderation, including fatty acids which is scored using an adequacy ratio of poly- and monounsaturated to saturated fat(Reference Guenther, Casavale and Reedy14).

For the population under study, we first examined the associations of socio-demographic and lifestyle variables with the exposure of interest, ACEs. More specifically, the variables included were age (as a continuous variable), BMI (in three categories: <25, 25–29⋅9, ≥30), education (in three categories: less than high school, high school or General Education Diploma (GED), more than high school), household income (in four categories: <$15 000, $15 000–<$25 000, $25 000–<$50 000, ≥$50 000), enrolment source (in two categories: community health centre, general population), marital status (in four categories: married or living as married, separated or divorced, widowed, single), neighbourhood deprivation index (in quartiles), smoking status (in four categories: never, former, current and <20 cigarettes per day, current and ≥20 cigarettes per day) and alcohol intake (in four categories: never or rarely, 1–3 times per month, 1–4 times per week, daily or near daily).

Statistical analysis

In order to explore the distribution of the socio-demographic and lifestyle variables by ACEs, we compared the mean of the continuous variable (age) and the frequencies of the categorical variables (all other variables, as listed above) across the five conventional ACE score categories, namely 0, 1, 2, 3 and 4 or more reported ACEs. Pearson χ 2 tests were utilised to determine the association of each respective categorical variable with the ACE score, and within each race/sex group. For age, student's t tests were used.

Similarly, we examined the distribution of the same baseline variables by the outcome HEI-10, in five categories of quintiles, with the fifth and highest quintile being the least healthy diet and the first and lowest quintile being the most healthy diet (this is the reverse of conventional HEI-10 scoring, but in line with the directionality of ACE scoring). Quintile categories were determined from the general population of participants and applied to each of the four race/sex groups. As in the baseline analysis by ACEs, associations between HEI-10 quintiles and each respective baseline variable were assessed using Pearson χ 2 tests and student's t tests for the continuous variable of age.

For the main analyses, ordinal logistic regression using proportional odds models were used to examine the association of ACEs with the outcome of HEI-10 in the same categories of quintiles. We also explored the association with a nominal polytomous model, with five potential outcomes (HEI-10 quintiles 1–5), but our analyses suggested that it was appropriate to use a simplified model with HEI-10 as one ordered categorical variable, with increasing quintile as the outcome. We calculated odds ratios (ORs) and 95 % confidence intervals (CIs) for increasing HEI-10 score (as a marker of worse diet quality) with the exposure of ACEs in four ways: by any ACE; by number of ACEs (in categories of 0, 1, 2, 3 and 4+); by ACE category (abuse, neglect, household dysfunction); with each of the ten individual ACEs. Having no ACEs at all, no ACEs for that category, and not having the individual ACE in question were used for reference.

Since ACEs occur in childhood, and all other data used in the present study, with the exception of race and sex, pertains to adulthood, variables associated with both ACEs and HEI-10 would not confound the association (as they would not affect the main exposure, of ACEs), and thus are presented to describe the population, but are not included as variables in the main results models.

As a secondary analysis, we included adult income as a variable, to determine the ACEs and HEI-10 association above and beyond the association with adult income, considering the higher cost of a high-quality diet. To do this, we used the same proportional odds models as discussed above, but then adjusted for adult annual household income in four categories: <$15 000; $15 000–$24 999; $25 000–$49 999; ≥$50 000 (using <$15 000 as the reference). As education was not associated with ACEs among all, and we found adjusting for education to have no effect on our ORs beyond adjustment for household income, we decided not to include it in our final analyses.

To further our understanding of the dietary contributors to the ACEs and HEI-10 association, we performed proportional odds logistic regression to calculate odds ratios of the exposure of any ACE and each HEI-10 component as an outcome. Again, we calculated ORs within each race/sex group and for all (adjusting for race and sex), and secondarily adjusting for annual household income.

Results

ACEs varied significantly with most adult socio-demographic and lifestyle variables (Table 1). In every race/sex group (Black females, Black males, White females and White males), more ACEs were reported by individuals who were younger, had lower household incomes were enrolled at a community health centre (v. the general population) were divorced or had never been married, and were smokers and drinkers. Among White females and White males only, a greater number of ACEs was also reported by obese individuals.

Table 1. Distribution of socio-demographic and lifestyle variables by number of adverse childhood experiences (ACEs), stratified by race and sex

Abbreviations: ACE, adverse childhood experiences; cpd, cigarettes per day.

1 Significant at P < 0⋅05 by ACE score for all.

2 Significant at P < 0⋅05 by ACE score for Black females.

3 Significant at P < 0⋅05 by ACE score for Black males.

4 Significant at P < 0⋅05 by ACE score for White females.

5 Significant at P < 0⋅05 by ACE score for White males.

The Healthy Eating Index-10 was also strongly associated with the adult socio-demographic and lifestyle variables (Table 2). In fact, every socio-demographic and lifestyle variable was associated with HEI-10 among all and in every race/sex group. In general, the trends found were similar to those in Table 1 with ACEs. For instance, a worse HEI-10 (represented by the highest quintile in the present study) was more common among younger individuals, people with lower household income, participants recruited from the community health centres (v. the general population), current smokers, frequent drinkers, and those who were divorced or never married, except for Black females, among whom divorced females were more likely to have a better HEI-10. While higher BMI was associated with worse HEI-10 among Whites, higher BMI was associated with better HEI-10 among Blacks. Unlike with ACEs, education was associated consistently and strongly with HEI-10, such that individuals with high school education or less were more likely to have worse HEI-10 across the race/sex groups than individuals with more than a high school education. Furthermore, current smoking, especially greater than 20 cigarettes per day, and more frequent alcohol intake were associated with worse HEI-10 in every race/sex group.

Table 2. Distribution of socio-demographic and lifestyle variables by Healthy Eating Index (HEI) quintile, stratified by race and sex

Abbreviations: cpd, cigarettes per day; HEI, Healthy Eating Index.

1 Significant at P < 0⋅05 by HEI score for all.

2 Significant at P < 0⋅05 by HEI score for Black females.

3 Significant at P < 0⋅05 by HEI score for Black males.

4 Significant at P < 0⋅05 by HEI score for White females.

5 Significant at P < 0⋅05 by HEI score for White males.

For the main analyses, being exposed to any childhood trauma (as defined by ACE screening) was associated with an increased odds of a worse HEI-10, compared to having no ACE (OR 1⋅22; 95 % CI 1⋅17, 1⋅27) (Table 3). This finding was consistent across all race/sex groups, and remained significant after adjusting for adult household income in the model. By including household income as a variable in the model, we estimated the effect of ACEs on diet quality above and beyond the association with adult household income. Thus, our adjusted results show a conservative estimate of the ACE-HEI association and suggest that there is a pathway from ACEs to diet quality outside of the association with income. Similarly, we found an increasing odds of worse HEI-10 with the increasing number of ACEs among all study participants and in every race/sex group before and after adjustment for income. Individuals with four or more ACEs have a 34 % increased relative odds of a worse HEI-10 compared to individuals with no ACEs (95 % CI 1⋅27, 1⋅42). By ACE category, associations were strongest for household dysfunction (all without income adjustment, OR 1⋅24; 95 % CI 1⋅19, 1⋅29; all with income adjustment, OR 1⋅16; 95 % CI 1⋅11, 1⋅20). For abuse, ORs were statistically significant without income adjustment and after adjustment (OR 1⋅12; 95 % CI 1⋅07, 1⋅17 and OR 1⋅06; 95 % CI 1⋅01, 1⋅11, respectively). Associations for neglect were stronger than for abuse, although not as strong as for household dysfunction, with ORs reaching 1⋅20 (95 % CI 1⋅15, 1⋅27) and 1⋅07 (95 % CI 1⋅02, 1⋅13) for before and after income adjustment. However, in the specific race/sex-specific groupings, neglect was significant after adjustment for income only among Black females (OR 1⋅09; 95 % CI 1⋅00, 1⋅18, respectively). Most of the ten individual ACEs were associated with HEI-10 both before and after adjustment for income. The only exceptions were for emotional abuse and physical neglect, which were significant before but not after income adjustment. The three strongest individual ACEs were significant before and after income adjustment among all and for three of the four race/sex groups. They were all household dysfunction ACEs, namely having a family member in prison (OR 1⋅34; 95 % CI 1⋅25, 1⋅42), having divorced or separated parents (OR 1⋅25; 95 % CI 1⋅20, 1⋅31), and living with alcohol or drug abuse (OR 1⋅19; 95 % CI 1⋅14, 1⋅25).

Table 3. Association of ACEs with a lower Healthy Eating Index, by race–sex groupings

1 Adjustment for income is in four categories (<$15 000; $15 000–<$25 000; $25 000–<$50 000; ≥ $50 000). The bold indicates statistically significant result at P<0.05

Reporting any ACE was associated broadly with the HEI-10 components (Table 4). In fact, every HEI-10 component was associated with any ACE in at least one race/sex group. Among all, every adequacy component was associated with any ACE except total protein foods. The strongest of these findings include a 26 % increase in odds of insufficient total fruit intake (OR 1⋅26; 95 % CI 1⋅21, 1⋅32), a 24 % increase in odds of insufficient whole fruit intake (OR 1⋅24; 95 % CI 1⋅19, 1⋅29) and a 13 % increase in odds of insufficient total vegetable intake (OR 1⋅13; 95 % CI 1⋅09, 1⋅18). Similarly, two of the three moderation components were associated with any ACE, namely solid fat/alcohol/sugar for an 18 % increase in odds of unhealthy excess (OR 1⋅18; 95 % CI 1⋅14, 1⋅23) and refined grains for a 4 % decrease in odds of unhealthy excess (OR 0⋅96; 95 % CI 0⋅92, 1⋅00).

Table 4. Association of adverse childhood experiences (ACEs) with HEI components

1 Adjustment for income is in four categories (<$15 000; $15 000–<$25 000; $25 000–<$50 000; ≥ $50 000). The bold indicates statistically significant result at P<0.05

For the secondary analysis adjusting for income, the associations among all remained in every component except whole grains and seafood and plant proteins. Furthermore, the components with the strongest associations before adjustment remained the strongest after adjustment, with adjusted ORs of 1⋅22 for total fruit (95 % CI 1⋅17, 1⋅27), 1⋅19 for whole fruit (95 % CI 1⋅14, 1⋅24) and 1⋅14 for solid fat/alcohol/added sugar (95 % CI 1⋅09, 1⋅18). These components were notably consistent across the race/sex groupings. For solid fat/alcohol/added sugar, ORs were significant in every case except after income adjustment for Black males. Additionally, we found there to be some race/sex-specific associations, the most notable being increased odds of insufficient greens and beans intake among Blacks (Black females, OR 1⋅11; 95 % CI 1⋅04, 1⋅19; Black males, OR 1⋅20; 95 % CI 1⋅09, 1⋅31) but not among Whites.

Discussion

Broadly, our findings demonstrate a positive association between ACEs, including any ACE, and worse adult diet quality. This is true for both Blacks and Whites, whether male or female, and is supported by the literature which describes ACEs as having a pervasive association with unhealthy behaviours and poor health across diverse populations(Reference Brockie, Elm and Walls43). Even further, our findings by number of ACEs suggest a dose-response effect. This suggests that the relationship found between ACEs and HEI-10 is causal. Nevertheless, our findings also indicate that the strength of the ACE-HEI association varies by race/sex group. This is consistent with the literature for the relationship between ACEs and other health outcomes(Reference Lee and Chen12,Reference Brown, Masho and Perera44) , and indicates that there may be additional factors at play within specific population demographics that need to be addressed in order to effectively estimate the ACE-HEI association in all subgroups.

Of particular interest are the strong associations found between household dysfunction ACEs and HEI-10. We believe that this may be in part due to the more objective aspect of the household dysfunction ACEs (compared to abuse or neglect ACEs), which include divorced parents, physically abused mother, living with alcohol or drug abuser, living with someone with mental illness and having a family member in prison. If this is the case, this also suggests that abuse and neglect ACEs may be underreported(Reference Della Femina, Yeager and Lewis45,Reference McKinney, Harris and Caetano46) , which would reduce our ability to detect an association between abuse and neglect ACEs with HEI-10. Another possibility is that household dysfunction ACEs truly are more likely to affect the dietary patterns experienced and learned by an individual as a child than abuse or neglect ACEs.

The strong connection between household functioning and health is supported by a study of 280 dyads in Miami, which found associations between self-report of parent–adolescent family functioning and obesity-related behaviours, specifically physical inactivity and poor diet, among Hispanic adolescents(Reference Lebron, Lee and Park47). Parent–adolescent discrepancy scores in family functioning were found to be negatively associated with both physically active days (β −0⋅14; 95 % CI −0⋅26, −0⋅05; P < 0⋅05) and fruit/vegetable intake (β −0⋅022; 95 % CI −0⋅38, −0⋅09; P < 0⋅001). Although the family functioning indicators (positive parenting, parental involvement, family communication, parental monitoring of peers and parent–adolescent communication) used by Lebron et al. were distinct from the household dysfunction ACEs, the findings on family dynamics and fruit/vegetable intake are consistent with the present study(Reference Lebron, Lee and Park47). Additionally, a recent cross-sectional study of 2939 adults using the 2017 Nevada Behavioral Risk Factor Surveillance System further supports our findings between household dysfunction, specifically parental divorce, and diet quality(Reference Horino and Yang48). In particular, having three or more ACEs (OR 1⋅42; 95 % CI 1⋅02, 2⋅00) and experiencing parental divorce or separation (OR 1⋅50; 95 % CI 1⋅13, 1⋅98) were found to be associated with lower consumption of fruit and vegetables(Reference Horino and Yang48).

Even further, the finding in the present study of household functioning and fruit/vegetable intake has been described internationally. In one recent study of 24 271 older adults in Japan, a sex-stratified multilevel Poisson regression found an association between ACEs and low fruit and vegetable intake that was more pronounced among females (1 ACE, OR 1⋅18; 95 % CI 1⋅07, 1⋅30; 2+ ACEs, OR 1⋅64; 95 % CI 1⋅42, 1⋅89) than males (1 ACE, OR 1⋅17; 95 % CI 1⋅08, 1⋅27; 2+ ACEs, OR 1⋅34; 95 % CI 1⋅20, 1⋅50)(Reference Yanagi, Inoue and Fujiwara49). Additionally, a study of 11 243 individuals in England by Russell et al. using the North West Mental Well-Being Survey found that adults with unhappy and violent childhoods had lower daily fruit and vegetable intake than adults with happy and non-violent childhoods (OR 2⋅67; 95 % CI 2⋅15, 3⋅06; P < 0⋅001). However, none of these studies were conducted in a largely low socioeconomic or racial/ethnic minority population(Reference Russell, Hughes and Bellis50).

In the present study, many ACE-HEI associations were particularly strong for White males. The reason for this is unclear. However, we suspect other factors are at play among marginalised groups which may have somewhat diminished our ability to detect the ACE-HEI association among non-White males. For instance, race/sex variations in resilience, exposure to other adverse experiences, and/or under-reporting may play a role. These variations could be specific to the largely low-income and Southern context of this population, or more generalisable by race and sex. Future research should explore these possibilities which may help explain the differences in the strength of the ACE-HEI associations by race and sex.

Importantly, there are likely a multitude of causal mechanisms through which ACE exposure leads to poor diet quality. We believe most of these pathways include neurobiological consequences of childhood trauma, where various neuroendocrine, neurochemical and neuroanatomic feature responses may all come into play(Reference Bose, Olivan and Laferrere51Reference Sominsky and Spencer56). The precise configuration of these responses could vary by the type of ACE, possibly even leading to different manifestations of poor adult diet quality (e.g. adequacy v. moderation components)(Reference Teicher and Samson57). Future studies are needed to explore potential pathways from childhood trauma to poor adult diet quality on the neurobiological level.

The present study suggests the need for interventions that can disrupt the pathway from ACEs to poor diet quality, and potentially downstream health outcomes. For example, ACE screening could be used as an important tool for identifying individuals at risk of poor diet quality and related health issues. Targeting individuals, households and/or communities with higher prevalence of ACEs, especially household dysfunction ACEs, could enhance the efficacy of dietary interventions and reduce disparities in ACE-related outcomes. In addition, interventions aimed at reducing the impact of traumatic experiences have the potential of positively impacting diet quality. Some examples of such interventions include Trauma-Focused Cognitive Behavioral Therapy (TF-CBT), Child-Parent Psychotherapy (CPP) and Eye Movement Desensitization and Reprocessing (EMDR)(Reference Carletto, Oliva and Barnato58Reference Hagan, Browne and Sulik61). On the structural level, trauma-informed care approaches should also be adopted and trauma-specific services be made available and affordable(Reference Branson, Baetz and Horwitz62Reference Wiest-Stevenson and Lee67). Importantly, the negative outcomes of childhood trauma appear throughout the lifespan, so it may never be too late to intervene. In fact, intervention with adults who were traumatised as children may not only improve health outcomes but decrease intergenerational transmission of trauma as well(Reference Dennis, Clohessy and Stone2).

To note, there are some limitations to the present study. These include a variety of factors that would have been useful to consider. For instance, we did not have the ages at which the ACEs occurred. Such detailed data would have been helpful since trauma tends to have a greater impact on younger children than older children(Reference De Bellis and Zisk68). Secondly, we did not have any information regarding childhood or young adult diet quality. This would be useful to explore when and why individuals with ACEs tend to develop worse diet quality. Similarly, household income as a child would have been useful to further validate the ACE-HEI association independent of income, rather than just adult household income as used in the present study. Where available, future studies should include these and other childhood lifestyle and environmental factors to consider the possibility of confounding, which could not be addressed by the present study. In addition, ACEs do not screen for all potentially traumatic childhood experiences (e.g. bullying, natural disaster, parent death), and HEI-10 may not account for all relevant adult dietary patterns (e.g. eating behaviours). Future studies using other or more extensive methods to estimate diet quality and childhood trauma would, thus, be useful to better understand the breadth of the associations described in the present paper. For instance, interviewing participants as well as their friends or family members could help better estimate childhood trauma and diet quality. This includes ACE severity and duration, which was not considered in the present study. Additionally, food diaries, resilience screening, and more prospective data collection (ACEs, HEI, household income, etc.) throughout childhood and adulthood may be valuable, as well as screening for adult adverse experiences. Health-related variables such as chronic disease, mental disorder, physical activity and sleep quality should also be considered for their potential role within or effect modification of the ACE-HEI pathway, although only socio-demographic and lifestyle variables were included in the study at hand.

Furthermore, the present study utilised self-report data to estimate both HEI-10 and ACE scores. It is possible that there is recall and reporting bias to our findings as a result, but whether this would bias our results towards or away from the null is not clear. Additionally, since participants were excluded who did not return for the second SCCS follow-up questionnaire (n 37 774), there may be a healthy worker selection bias to our findings which would bias our results towards the null. The included participants still represent an overall low SES population (as 46 % of the participants in the present study have an annual household income of less than $15 000), but as mentioned earlier the representation of the very lowest socioeconomic position is consequently less strong. Our results could similarly be biased towards the null by the smaller exclusion of participants (n 5715) who returned for the second SCCS follow-up questionnaire but did not complete one or more ACE questions within it, since such omissions may reflect sensitivity to the ACE questions.

There are other potential complications to our study as well, which may make our findings more difficult to interpret. For instance, there is research suggesting that poor childhood diet could make children more susceptible to the neurobiological impacts of trauma, as well as research suggesting that good diet quality may help mitigate the impact of trauma(Reference Ebenezer, Wilson and Wilson69,Reference Kalyan-Masih, Vega-Torres and Miles70) . As a result, the associations found with poor diet quality could reflect a reporting bias where individuals with poorer adult diet quality are more likely to qualify their childhood experiences as significant or traumatic depending on the pervasiveness of their experience determined by childhood or adult diet quality. Additionally, there is research suggesting women with ACEs who consequently develop a dysregulated HPA axis can pass on or ‘transmit’ HPA dysregulation to their child during pregnancy, and that a high-quality diet during pregnancy can mitigate this impact by positively modifying the stress response through dietary factors such as prenatal maternal choline intake(Reference Vaghef-Mehrabani, Thomas-Argyriou and Lewis71). Taking this mechanism of intergenerational trauma into account, the trauma and even diet of our participants’ birth mothers could be in part responsible for participant adult dietary quality in the present study. This effect could be compounded after birth through other factors such as emotional feeding practices, family stress internalisation and parental food purchasing behaviours(Reference Schuler, Vazquez and Kobulsky28,Reference O'Connor, Huh and Schembre72) . Thus, the ACE-HEI association found could reflect not only the trauma experienced by our participants themselves, but the trauma passed down in utero or during childhood. This, however, also raises the possibility of a diminished ability to detect association in the present study, since it is possible for an individual impacted by generational trauma to have avoided the traumatic childhood experiences screened for while still being adversely impacted by trauma throughout their life (e.g. diet quality). Nevertheless, the implications of our study remain the same whether or not these phenomena play an explanatory role in our findings: diet quality should be paid greater attention to for people who have experienced childhood trauma, trauma interventions could be useful to improve poor diet quality, and efforts to intercede in the ACE-HEI pathway could reduce health disparities, disease and mortality rates.

The present study had notable strengths as well. First, the large sample size of 30 854 participants supports the precision of the association found between ACEs and HEI-10. Second, this large sample size, particularly among Blacks, allowed us to conduct race/sex-specific analyses, finding both universal prevalence of the association and consistent manifestations by race and sex. Third, there were notable strengths regarding questionnaire design. The FFQ utilised by the SCCS was designed to account for the race and geographic region, and most SCCS participants completed the FFQ through an in-person computer-assisted interview. Telephone administration was offered for the second follow-up questionnaire which included the ACE questionnaire, and the ACE questionnaire that was utilised modelled the standardised framework for ACE assessment. Furthermore, the questions on the ACE questionnaire used were succinct to prevent burnout, but also highly specific to maximise objectivity, aid validity and prevent misclassification bias(Reference Rariden, SmithBattle and Yoo73). Moreover, a comprehensive dietary assessment was used to analyze the relationship between ACEs and diet quality, which no other study has done to date. In addition, component analysis in the present study supports the conclusion that ACEs are broadly associated with poor adult diet quality. Lastly, the present study allowed us to examine the association of ACEs and HEI-10 independent of household income, which could play a significant role due to the high cost of a high-quality diet(Reference Jackson, Chilton and Johnson74).

In conclusion, in this large study of primarily low-income individuals in the southeastern US, having had any ACE was associated with an increased odds of a worse diet quality as an adult. This association was consistent among Blacks and Whites, and males and females, and became stronger with increasing number of ACEs. Moreover, adjusting for adult SES, as estimated by household income, did not remove the association. As diet quality is directly linked to health outcomes, our study suggests that further research is needed to understand the mechanisms through which ACEs increase the likelihood of poor adult diet, and thus the potential for dietary and therapeutic interventions to improve health outcomes among individuals who have experienced childhood trauma.

Acknowledgements

Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under Award Number U01CA202979. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. SCCS data collection was performed by the Survey and Biospecimen Shared Resource which is supported in part by the Vanderbilt-Ingram Cancer Center (P30 CA68485).

S. R. A. conceived the original idea and performed the statistical analysis; M. E. and S. R. A. developed the overall research plan, analysed the data, interpreted the data, drafted the manuscript and have primary responsibility for the final content; M. J. S. helped develop the overall research plan and acquire the data; J. B. also helped develop the overall research plan; M. J. S., J. B., M. S., D. G. S. and M. C. C. offered key insights and critical feedback on the preliminary data and drafted manuscript. All authors interpreted the data, discussed the results and approved the final manuscript.

The authors declare that they have no conflict of interest.

This study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving research study participants were approved by the Institutional Review Boards of Vanderbilt University and Meharry Medical College. Written informed consent was obtained from all subjects.

References

Felitti, VJ, Anda, RF, Nordenberg, D, et al. (1998) Relationship of childhood abuse and household dysfunction to many of the leading causes of death in adults. The Adverse Childhood Experiences (ACE) Study. Am J Prev Med 14, 245258.CrossRefGoogle ScholarPubMed
Dennis, CH, Clohessy, DS, Stone, AL, et al. (2019) Adverse childhood experiences in mothers with chronic pain and intergenerational impact on children. J Pain 20, 12091217.CrossRefGoogle ScholarPubMed
Kia-Keating, M, Barnett, ML, Liu, SR, et al. (2019) Trauma-responsive care in a pediatric setting: feasibility and acceptability of screening for adverse childhood experiences. Am J Community Psychol 64, 286297.CrossRefGoogle Scholar
Martin-Higarza, Y, Fontanil, Y, Mendez, MD, et al. (2020) The direct and indirect influences of adverse childhood experiences on physical health: a cross-sectional study. Int J Environ Res Public Health 17, 8507.CrossRefGoogle ScholarPubMed
Windle, SB, Dehghani, P, Roy, N, et al. (2018) Smoking abstinence 1 year after acute coronary syndrome: follow-up from a randomized controlled trial of varenicline in patients admitted to hospital. CMAJ 190, E347EE54.CrossRefGoogle ScholarPubMed
Ports, KA, Holman, DM, Guinn, AS, et al. (2019) Adverse childhood experiences and the presence of cancer risk factors in adulthood: a scoping review of the literature from 2005 to 2015. J Pediatr Nurs 44, 8196.CrossRefGoogle ScholarPubMed
Amemiya, A, Fujiwara, T, Shirai, K, et al. (2019) Association between adverse childhood experiences and adult diseases in older adults: a comparative cross-sectional study in Japan and Finland. BMJ Open 9, e024609.CrossRefGoogle Scholar
Waehrer, GM, Miller, TR, Silverio Marques, SC, et al. (2020) Disease burden of adverse childhood experiences across 14 states. PLoS ONE 15, e0226134.CrossRefGoogle ScholarPubMed
Merrick, MT, Ford, DC, Ports, KA, et al. (2019) Vital signs: estimated proportion of adult health problems attributable to adverse childhood experiences and implications for prevention - 25 states, 2015-2017. MMWR Morb Mortal Wkly Rep 68, 9991005.CrossRefGoogle ScholarPubMed
Deschenes, SS, Graham, E, Kivimaki, M, et al. (2018) Adverse childhood experiences and the risk of diabetes: examining the roles of depressive symptoms and cardiometabolic dysregulations in the Whitehall II Cohort Study. Diabetes Care 41, 21202126.CrossRefGoogle ScholarPubMed
Kenney, MK & Singh, GK (2016) Adverse childhood experiences among American Indian/Alaska Native children: the 2011-2012 national survey of children's health. Scientifica (Cairo) 2016, 7424239.Google ScholarPubMed
Lee, RD & Chen, J (2017) Adverse childhood experiences, mental health, and excessive alcohol use: examination of race/ethnicity and sex differences. Child Abuse Negl 69, 4048.CrossRefGoogle ScholarPubMed
Mersky, J, Topitzes, J & Reynolds, A (2013) Impacts of adverse childhood experiences on health, mental health, and substance use in early adulthood: a cohort study of an urban, minority sample in the U.S. Child Abuse Negl 37, 917925.CrossRefGoogle ScholarPubMed
Guenther, PM, Casavale, KO, Reedy, J, et al. (2013) Update of the Healthy Eating Index: HEI-2010. J Acad Nutr Diet 113, 569580.CrossRefGoogle ScholarPubMed
Guenther, PM, Kirkpatrick, SI, Reedy, J, et al. (2014) The Healthy Eating Index-2010 is a valid and reliable measure of diet quality according to the 2010 Dietary Guidelines for Americans. J Nutr 144, 399407.CrossRefGoogle ScholarPubMed
Anda, RF, Felitti, VJ, Bremner, JD, et al. (2006) The enduring effects of abuse and related adverse experiences in childhood. A convergence of evidence from neurobiology and epidemiology. Eur Arch Psychiatry Clin Neurosci 256, 174186.CrossRefGoogle ScholarPubMed
Coffino, JA, Grilo, CM & Udo, T (2020) Childhood food neglect and adverse experiences associated with DSM-5 eating disorders in U.S. National Sample. J Psychiatr Res 127, 7579.CrossRefGoogle ScholarPubMed
Deighton, S, Neville, A, Pusch, D, et al. (2018) Biomarkers of adverse childhood experiences: a scoping review. Psychiatry Res 269, 719732.CrossRefGoogle ScholarPubMed
Dempster, KS, O'Leary, DD, MacNeil, AJ, et al. (2021) Linking the hemodynamic consequences of adverse childhood experiences to an altered HPA axis and acute stress response. Brain Behav Immun 93, 254263.CrossRefGoogle Scholar
Hantsoo, L, Jasarevic, E, Criniti, S, et al. (2019) Childhood adversity impact on gut microbiota and inflammatory response to stress during pregnancy. Brain Behav Immun 75, 240250.CrossRefGoogle ScholarPubMed
Harada, M, Guerrero, A, Iyer, S, et al. (2021) The relationship between adverse childhood experiences and weight-related health behaviors in a national sample of children. Acad Pediatr. S1876-2859(21)000276-XCrossRefGoogle Scholar
Holgerson, AA, Clark, MM, Ames, GE, et al. (2018) Association of adverse childhood experiences and food addiction to bariatric surgery completion and weight loss outcome. Obes Surg 28, 33863392.CrossRefGoogle ScholarPubMed
John-Henderson, NA, Henderson-Matthews, B, Ollinger, SR, et al. (2020) Adverse childhood experiences and immune system inflammation in adults residing on the Blackfeet reservation: the moderating role of sense of belonging to the community. Ann Behav Med 54, 8793.CrossRefGoogle ScholarPubMed
Park, SH, Videlock, EJ, Shih, W, et al. (2016) Adverse childhood experiences are associated with irritable bowel syndrome and gastrointestinal symptom severity. Neurogastroenterol Motil 28, 12521260.CrossRefGoogle ScholarPubMed
Rasmussen, LJH, Moffitt, TE, Arseneault, L, et al. (2020) Association of adverse experiences and exposure to violence in childhood and adolescence with inflammatory burden in young people. JAMA Pediatr 174, 3847.CrossRefGoogle ScholarPubMed
Wiss, DA & Brewerton, TD (2020) Adverse childhood experiences and adult obesity: a systematic review of plausible mechanisms and meta-analysis of cross-sectional studies. Physiol Behav 223, 112964.CrossRefGoogle ScholarPubMed
Witges, KM, Bernstein, CN, Sexton, KA, et al. (2019) The relationship between adverse childhood experiences and health care use in the Manitoba IBD Cohort Study. Inflamm Bowel Dis 25, 17001710.CrossRefGoogle ScholarPubMed
Schuler, BR, Vazquez, C, Kobulsky, JM, et al. (2021) The early effects of cumulative and individual adverse childhood experiences on child diet: examining the role of socioeconomic status. Prev Med 145, 106447.CrossRefGoogle ScholarPubMed
Baskind, MJ, Taveras, EM, Gerber, MW, et al. (2019) Parent-perceived stress and its association with children's weight and obesity-related behaviors. Prev Chronic Dis 16, E39.CrossRefGoogle ScholarPubMed
Gentner, MB & Leppert, MLO (2019) Environmental influences on health and development: nutrition, substance exposure, and adverse childhood experiences. Dev Med Child Neurol 61, 10081014.CrossRefGoogle ScholarPubMed
Lackner, CL, Santesso, DL, Dywan, J, et al. (2018) Adverse childhood experiences are associated with self-regulation and the magnitude of the error-related negativity difference. Biol Psychol 132, 244251.CrossRefGoogle ScholarPubMed
Lu, S, Xu, R, Cao, J, et al. (2019) The left dorsolateral prefrontal cortex volume is reduced in adults reporting childhood trauma independent of depression diagnosis. J Psychiatr Res 112, 1217.CrossRefGoogle ScholarPubMed
McEwen, BS (2017) Neurobiological and systemic effects of chronic stress. Chronic Stress (Thousand Oaks) 1, 2470547017692328.Google ScholarPubMed
Miguel, PM, Pereira, LO, Silveira, PP, et al. (2019) Early environmental influences on the development of children's brain structure and function. Dev Med Child Neurol 61, 11271133.CrossRefGoogle ScholarPubMed
Signorello, LB, Hargreaves, MK & Blot, WJ (2010) The Southern Community Cohort Study: investigating health disparities. J Health Care Poor Underserved 21, 2637.CrossRefGoogle ScholarPubMed
Hargreaves, MK, Mouton, CP, Liu, J, et al. (2019) Adverse childhood experiences and health care utilization in a low-income population. J Health Care Poor Underserved 30, 749767.CrossRefGoogle Scholar
Mouton, CP, Hargreaves, MK, Liu, J, et al. (2016) Adult cancer risk behaviors associated with adverse childhood experiences in a low income population in the southeastern United States. J Health Care Poor Underserved 27, 6883.CrossRefGoogle Scholar
Yu, D, Sonderman, J, Buchowski, MS, et al. (2015) Healthy eating and risks of total and cause-specific death among low-income populations of African-Americans and other adults in the southeastern United States: a prospective cohort study. PLoS Med 12, e1001830; discussion e1001830.CrossRefGoogle ScholarPubMed
Dube, SR, Williamson, DF, Thompson, T, et al. (2004) Assessing the reliability of retrospective reports of adverse childhood experiences among adult HMO members attending a primary care clinic. Child Abuse Negl 28, 729737.CrossRefGoogle ScholarPubMed
Wade, R Jr, Becker, BD, Bevans, KB, et al. (2017) Development and evaluation of a short adverse childhood experiences measure. Am J Prev Med 52, 163172.CrossRefGoogle Scholar
Buchowski, MS, Schlundt, DG, Hargreaves, MK, et al. (2003) Development of a culturally sensitive food frequency questionnaire for use in the Southern Community Cohort Study. Cell Mol Biol (Noisy-le-grand) 49, 12951304.Google ScholarPubMed
Signorello, LB, Munro, HM, Buchowski, MS, et al. (2009) Estimating nutrient intake from a food frequency questionnaire: incorporating the elements of race and geographic region. Am J Epidemiol 170, 104111.CrossRefGoogle ScholarPubMed
Brockie, TN, Elm, JHL & Walls, ML (2018) Examining protective and buffering associations between sociocultural factors and adverse childhood experiences among American Indian adults with type 2 diabetes: a quantitative, community-based participatory research approach. BMJ Open 8, e022265.CrossRefGoogle ScholarPubMed
Brown, MJ, Masho, SW, Perera, RA, et al. (2017) Sex disparities in adverse childhood experiences and HIV/STIs: mediation of psychopathology and sexual behaviors. AIDS Behav 21, 15501566.CrossRefGoogle ScholarPubMed
Della Femina, D, Yeager, CA & Lewis, DO (1990) Child abuse: adolescent records vs. adult recall. Child Abuse Negl 14, 227231.CrossRefGoogle ScholarPubMed
McKinney, CM, Harris, TR & Caetano, R (2009) Reliability of self-reported childhood physical abuse by adults and factors predictive of inconsistent reporting. Violence Vict 24, 653668.CrossRefGoogle ScholarPubMed
Lebron, CN, Lee, TK, Park, SE, et al. (2018) Effects of parent-adolescent reported family functioning discrepancy on physical activity and diet among Hispanic youth. J Fam Psychol 32, 333342.CrossRefGoogle ScholarPubMed
Horino, M & Yang, W (2020) Impact of adverse childhood experiences and fruit and vegetable intake in adulthood. Public Health Nutr 24, 10341041.CrossRefGoogle ScholarPubMed
Yanagi, N, Inoue, Y, Fujiwara, T, et al. (2020) Adverse childhood experiences and fruit and vegetable intake among older adults in Japan. Eat Behav 38, 101404.CrossRefGoogle ScholarPubMed
Russell, SJ, Hughes, K & Bellis, MA (2016) Impact of childhood experience and adult well-being on eating preferences and behaviours. BMJ Open 6, e007770.CrossRefGoogle ScholarPubMed
Bose, M, Olivan, B & Laferrere, B (2009) Stress and obesity: the role of the hypothalamic-pituitary-adrenal axis in metabolic disease. Curr Opin Endocrinol Diabetes Obes 16, 340346.CrossRefGoogle ScholarPubMed
Cross, D, Fani, N, Powers, A, et al. (2017) Neurobiological development in the context of childhood trauma. Clin Psychol (New York) 24, 111124.Google ScholarPubMed
Heany, SJ, Groenewold, NA, Uhlmann, A, et al. (2018) The neural correlates of childhood trauma questionnaire scores in adults: a meta-analysis and review of functional magnetic resonance imaging studies. Dev Psychopathol 30, 14751485.CrossRefGoogle ScholarPubMed
Price, M, Albaugh, M, Hahn, S, et al. (2021) Examination of the association between exposure to childhood maltreatment and brain structure in young adults: a machine learning analysis. Neuropsychopharmacology 46, 18881894.CrossRefGoogle ScholarPubMed
Sherin, JE & Nemeroff, CB (2011) Post-traumatic stress disorder: the neurobiological impact of psychological trauma. Dialogues Clin Neurosci 13, 263278.Google ScholarPubMed
Sominsky, L & Spencer, SJ (2014) Eating behavior and stress: a pathway to obesity. Front Psychol 5, 434.CrossRefGoogle ScholarPubMed
Teicher, MH & Samson, JA (2013) Childhood maltreatment and psychopathology: a case for ecophenotypic variants as clinically and neurobiologically distinct subtypes. Am J Psychiatry 170, 11141133.CrossRefGoogle ScholarPubMed
Carletto, S, Oliva, F, Barnato, M, et al. (2017) EMDR as add-on treatment for psychiatric and traumatic symptoms in patients with substance use disorder. Front Psychol 8, 2333.CrossRefGoogle ScholarPubMed
de Arellano, MA, Lyman, DR, Jobe-Shields, L, et al. (2014) Trauma-focused cognitive-behavioral therapy for children and adolescents: assessing the evidence. Psychiatr Serv 65, 591602.CrossRefGoogle ScholarPubMed
Gilgoff, R, Singh, L, Koita, K, et al. (2020) Adverse childhood experiences, outcomes, and interventions. Pediatr Clin North Am 67, 259273.CrossRefGoogle ScholarPubMed
Hagan, MJ, Browne, DT, Sulik, M, et al. (2017) Parent and child trauma symptoms during child-parent psychotherapy: a prospective cohort study of dyadic change. J Trauma Stress 30, 690697.CrossRefGoogle ScholarPubMed
Branson, CE, Baetz, CL, Horwitz, SM, et al. (2017) Trauma-informed juvenile justice systems: a systematic review of definitions and core components. Psychol Trauma 9, 635646.CrossRefGoogle ScholarPubMed
Levenson, J (2017) Trauma-informed social work practice. Soc Work 62, 105113.Google ScholarPubMed
Li, Y, Cannon, LM, Coolidge, EM, et al. (2019) Current state of trauma-informed education in the health sciences: lessons for nursing. J Nurs Educ 58, 93101.CrossRefGoogle ScholarPubMed
Oral, R, Ramirez, M, Coohey, C, et al. (2016) Adverse childhood experiences and trauma informed care: the future of health care. Pediatr Res 79, 227233.CrossRefGoogle ScholarPubMed
Reeves, E (2015) A synthesis of the literature on trauma-informed care. Issues Ment Health Nurs 36, 698709.CrossRefGoogle ScholarPubMed
Wiest-Stevenson, C & Lee, C (2016) Trauma-informed schools. J Evid Inf Soc Work 13, 498503.CrossRefGoogle ScholarPubMed
De Bellis, MD & Zisk, A (2014) The biological effects of childhood trauma. Child Adolesc Psychiatr Clin N Am 23, 185222, vii.CrossRefGoogle ScholarPubMed
Ebenezer, PJ, Wilson, CB, Wilson, LD, et al. (2016) The anti-inflammatory effects of blueberries in an animal model of post-traumatic stress disorder (PTSD). PLoS ONE 11, e0160923.CrossRefGoogle Scholar
Kalyan-Masih, P, Vega-Torres, JD, Miles, C, et al. (2016) Western high-fat diet consumption during adolescence increases susceptibility to traumatic stress while selectively disrupting hippocampal and ventricular volumes. eNeuro 3, ENEURO.0125-16.2016.CrossRefGoogle ScholarPubMed
Vaghef-Mehrabani, E, Thomas-Argyriou, JC, Lewis, ED, et al. (2021) The role of maternal nutrition during pregnancy in the intergenerational transmission of childhood adversity. Psychoneuroendocrinology 130, 105283.CrossRefGoogle ScholarPubMed
O'Connor, SG, Huh, J, Schembre, SM, et al. (2019) The association of maternal perceived stress with changes in their children's Healthy Eating Index (HEI-2010) scores over time. Ann Behav Med 53, 877885.CrossRefGoogle ScholarPubMed
Rariden, C, SmithBattle, L, Yoo, JH, et al. (2021) Screening for adverse childhood experiences: literature review and practice implications. J Nurse Pract 17, 98104.CrossRefGoogle ScholarPubMed
Jackson, DB, Chilton, M, Johnson, KR, et al. (2019) Adverse childhood experiences and household food insecurity: findings from the 2016 national survey of children's health. Am J Prev Med 57, 667674.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Distribution of socio-demographic and lifestyle variables by number of adverse childhood experiences (ACEs), stratified by race and sex

Figure 1

Table 2. Distribution of socio-demographic and lifestyle variables by Healthy Eating Index (HEI) quintile, stratified by race and sex

Figure 2

Table 3. Association of ACEs with a lower Healthy Eating Index, by race–sex groupings

Figure 3

Table 4. Association of adverse childhood experiences (ACEs) with HEI components