Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-26T07:36:43.276Z Has data issue: false hasContentIssue false

Changes in bone mineral density of adolescent mothers during the 12-month postpartum period

Published online by Cambridge University Press:  03 December 2009

Agustina Malpeli
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
José L Mansur
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
Soledad De Santiago
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
Rosa Villalobos
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
Alicia Armanini
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
María Apezteguía
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
Horacio F González*
Affiliation:
Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Hospital de Niños de La Plata (MS/CIC-PBA), 63 Nº 1069 La Plata CP 1900, Argentina
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective

Bone mineral density (BMD) loss has been described in adult women in the 12-month postpartum period. However, little is known about the precise BMD pattern in adolescent mothers. The present study aimed to evaluate BMD in Argentinean adolescent mothers followed up during the 12-month postpartum period.

Design

Analytical, prospective clinical trial. BMD and body composition were determined by dual-energy X-ray absorptiometry; bone mineral content (BMC) and BMD were measured in the lumbar spine (L2–L4), femoral neck (FN), femur trochanter (TR), total hip (TH) and total body. Changes in BMD and BMC were analysed using ANOVA for pairwise comparisons. Other comparisons were performed with the paired-sample t test and Wilcoxon test; Pearson’s correlation coefficient was used to analyse the relationship among continuous variables.

Setting

La Plata, Argentina.

Subjects

Adolescent mothers (n 35; 17 years old or less) were recruited within 15 d after delivery. Studies and follow-up were performed at 15 d and 3, 6 and 12 months postpartum.

Results

BMD and BMC losses at 3 and 6 months and recovery at 12 months fitted a quadratic curve (ANOVA) at the three sites studied (FN, TH, TR), in total-body BMD (P = 0·000) and BMC (P = 0·038). At hip sites, BMD loss occurred at 3 months (FN, P = 0·000; TR, P = 0·000; TH, P = 0·000) and 6 months (FN, P = 0·000; TR, P = 0·000; TH, P = 0·000) compared with basal values. Percentage BMD loss immediately after delivery up to 6 months was about 5 %.

Conclusions

Adolescents showed significant BMD and BMC losses at 6 months postpartum, with an almost total recovery at 12 months in all sites studied.

Type
Research paper
Copyright
Copyright © The Authors 2009

Bone mineral density (BMD) loss has been described in adult women during the 12-month postpartum period(Reference Laskey and Prentice1, Reference Kalkwarf and Specker2). However, little is known about the precise pattern of recovery in adolescent mothers.

Different factors influence bone mass, including hereditary factors, intake of Ca and vitamin D, body weight, age, reproductive history (age at menarche, consumption of oral contraceptives, age at first pregnancy, interval between births, parity) and lifestyle habits (alcohol consumption, physical activity, smoking, sun exposure)(Reference Mazzes and Barden3).

During puberty, bone accretion is associated with increments in skeletal length and mass that increase Ca demands; approximately 40 % of bone mass is accumulated in this period(Reference Gong and Heald4, Reference Weaver, Peacock and Martin5). In pregnant adolescents, Ca is required for fetal bone formation(Reference Forbes6) and for the continuous demand of the maternal skeleton, which is still growing(Reference Bailey, Martin and McKay7). During lactation, Ca is needed for maternal milk(Reference Laskey, Prentice and Hanratty8). Although intestinal Ca absorption increases during pregnancy, it remains the same as before pregnancy during lactation. However, urinary Ca elimination increases during pregnancy, returns to pre-pregnancy levels during lactation, and is lower than baseline at the post-weaning period. This is probably due to hormonal changes, although the mechanisms are poorly understood(Reference Cross, Hillman and Allen9).

Adult lactating women lose BMD, particularly at trabecular bone sites. Such loss occurs during months 3–6 of lactation, affecting lumbar spine and femoral neck by 3 to 5 %. These percentages are higher than those observed in early menopause during the same period(Reference Kovacs10).

The aim of the present study was to evaluate BMD in adolescents from Argentina followed up for 12 months postpartum.

Methods

The study employed an analytical, prospective clinical design to assess thirty-five adolescent mothers recruited within 15 d after delivery from the Maternity Department at the Hospital General de Agudos ‘José de San Martín’, La Plata, Argentina. Follow-ups were performed at the Outpatient Ward of the Instituto de Desarrollo e Investigaciones Pediátricas ‘Prof. Fernando E. Viteri’ (IDIP), Children’s Hospital ‘Sor Maria Ludovica’, La Plata, Argentina.

Women included in the study were healthy, ≤17 years of age, with BMI of 18·5–24·9 kg/m2, primiparous, with a term singleton pregnancy (newborn birth weight ≥2500 g), exclusively breast-feeding for at least 3 months, and using natural contraceptive methods or an intra-uterine device. Exclusion criteria were the presence of chronic and/or acute diseases, history of rickets and osteomalacia, infectious disease the time of the study, use of any medication, use of Ca and/or vitamin D supplements, drug consumption, and not willing to participate in the study.

The study protocol was approved by the Ethical Committee of the Hospital General de Agudos ‘José de San Martin’, La Plata, Argentina.

A social worker surveyed the adolescent mothers within 15 d after delivery, and invited those who complied with the inclusion criteria to participate in the study. Written informed consent was obtained from each adolescent and a responsible adult. Studies and follow-ups were performed at 15 d and at 3, 6 and 12 months postpartum. A general clinical examination was done before starting the trial, and a questionnaire about breast-feeding, resumption of menses and contraceptive methods was also performed by the nutritionist and the clinician.

Body weight was measured electronically with a Tanita 1582 digital balance (100 g accuracy) and height was measured with a SECA 222 stadiometer (mm graduation, 1 cm accuracy) at each visit.

The food-frequency method(Reference Hankin11) was used to survey dietary intake; according to the food ingested, the amount of nutrient consumption per day was calculated, estimating daily intake of energy (kJ/d, kcal/d), proteins (g/d), Ca (mg/d), P (mg/d) and vitamin D (IU/d) with the US Department of Agriculture food composition database(12).

Overall physical activity was classified according to intensity of effort and time engaged in activity such as resting and very light, light, moderate and heavy work(13).

Bone mineral densitometry was performed by dual-energy X-ray absorptiometry (DEXA) with a LUNAR DPX-L instrument with paediatric software version 4·6f (GE Lunar Corporation, Madison, WI, USA). BMD CV% in vivo (reproducibility): lumbar spine (L2–L4), 1·3 %; femoral neck (FN) 1·5 %; femur trochanter (TR), 1·4 %; total hip (TH), 0·9 %; total body, 0·8 %. Studies were performed by a single expert observer. Bone mineral content (BMC) and total-body BMD were determined; BMD was also measured in L2–L4, FN, TR and TH. Body composition was also estimated by DEXA(Reference Brunton, Bayley and Atkinson14, Reference Mazzes, Barden and Bisek15).

Adolescent mothers were further divided into two groups, younger (14–15 years) and older (16–17 years) mothers, to analyse changes in BMC during the study period.

Statistical analysis

Repeated-measures ANOVA with pairwise comparisons with Bonferroni adjustment to the significance was used to study changes in BMD and BMC. Repeated-measures ANOVA was also used to compare BMC between older and younger mothers. Basal (15 d) v. 3-, 6- and 12-month values were compared with the paired-samples t test for anthropometric variables and the Wilcoxon test for nutrient intake. The relationship among continuous variables was analysed with Pearson’s correlation coefficient. Student’s t test was used to compare BMD and BMC in mothers who had or had not resumed menses at 3 months postpartum.

Results

Mean age at entry in the study was 15·43 (sd 0·81) years; mean age at onset of menarche was 12 (sd 0·92) years. All adolescents belonged to low-income families receiving care at a public maternity unit of the Province of Buenos Aires, and practised light physical activity. During pregnancy, mean weight gain had been 14·7 (sd 5·8) kg.

Follow-up of infants from participating mothers was performed every month, and that of mothers was at 16 (sd 2), 88 (sd 5), 172 (sd 9) and 368 (sd 15) d.

Table 1 presents the results of the dietary surveys. A significant decrease in energy and intake of other nutrients can be observed from month 3 postpartum onwards. Of the total number of mothers, 82 % continued breast-feeding their infants 12 months after delivery.

Table 1 Dietary survey results at baseline and different times postpartum: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

Statistical comparisons are between measures at different postpartum months.

Table 2 shows the anthropometric characteristics of the adolescent mothers 15 d and 3, 6 and 12 months postpartum. Mean height at baseline was 155·5 (sd 6·4) cm. Weight and BMI decreased significantly from 3 to 6 months postpartum, whereas the percentage of fat mass decreased significantly and progressively from 15 d to 12 months postpartum. Lean mass increased by 1·13 kg from 15 d to 12 months postpartum (P < 0·001), and fat mass loss was 4·5 kg (P < 0·001).

Table 2 Anthropometric parameters during the 12-month postpartum period: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

DEXA, dual-energy X-ray absorptiometry.

Statistical comparisons are between measures at different postpartum months.

At 12 months, there was a positive correlation between body weight and total-body BMD (r = 0·468; P = 0·007) and between body weight and BMC (r = 0·490; P = 0·004). Likewise, there was a positive and statistically significant correlation between BMI and total-body BMD (r = 0·527; P = 0·002) and between BMI and BMC (r = 0·427; P = 0·015).

Figure 1 shows changes in BMD and BMC in the 12-month postpartum period. Losses at 3 and 6 months and recovery at 12 months fitted a quadratic curve according to repeated-measures ANOVA at the three hip sites studied (FN, TH, TR), in total-body BMD (P = 0·000) and BMC (P = 0·038).

Fig. 1 Bone mineral density (BMD) at the different sites studied (, lumbar spine; , femur trochanter; , femoral neck; , total hip; , total body) at baseline (within 15 d after delivery) and 90, 180 and 360 d postpartum: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

At hip sites, BMD loss occurred at 3 months (FN, P = 0·000; TR, P = 0·000; TH, P = 0·000) and at 6 months (FN, P = 0·000; TR, P = 0·000; TH, P = 0·000) compared with basal values. Percentage BMD loss immediately after delivery up to 6 months was about 5 %. Similarly, losses in total-body BMD were significant at 3 (P = 0·019) and 6 (P = 0·004) months compared with values recorded 15 d postpartum.

Bonferroni test could not show statistically significant changes in BMC at any study point. Losses in total-body BMD and BMC were about 2 %.

Figure 1 shows that recovery in BMC, hip and total-body BMD was almost complete 12 months postpartum. Although there were no significant BMD losses in L2–L4 during the first 6 months postpartum, there was a significant increase from 6 to 12 months (P = 0·000). Changes also fitted a quadratic model according to repeated-measures ANOVA (P = 0·000). At 12 months, adolescents gained 6 % more than their basal value.

The impact of menses resumption on BMD was assessed by comparing BMD recovery at 12 months postpartum between adolescent mothers who had resumed menses at 3 months (Group 1) and those who were still amenorrhoeic during the same period (Group 2). Differences in total-body, hip and lumbar spine BMD between groups are shown in Table 3. Despite a slightly higher recovery in adolescents who had resumed menses, differences were not significant at the different hip sites and in BMC.

Table 3 BMD and BMC recovery at 12 months postpartum at the different sites studied, according to resumption of menses: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

BMD, bone mineral density; BMC, bone mineral content; Group 1, adolescent mothers who had resumed menses at 3 months; Group 2, those who had not.

Regarding BMC in the two age groups of adolescent mothers at 15 d, it was slightly higher in older adolescents: 2·244 (sd 0·263) g v. 2·099 (sd 0·197) g (P = 0·080). At 12 months postpartum, BMC was 2·255 (sd 0·280) v. 2·081 (sd 0·189) g (P = 0·053) in older and younger adolescents, respectively. Older adolescents had higher values than younger ones during the study period (P = 0·019; Fig. 2).

Fig. 2 Bone mineral content (BMC) at baseline (within 15 d after delivery) and 90, 180 and 360 d postpartum according to age (—⧫—, 14–15 years; —▪—, 16–17 years): adolescent mothers (n 35), La Plata, Argentina

Discussion

Adolescents who become mothers are a particularly vulnerable nutritional group due to the enhanced nutrient demands of pregnancy and lactation and their demands for growth(Reference Ward, Adams and Mughal16). To our knowledge, the present study is the first detailed longitudinal study in adolescent mothers where dietary intakes, changes in body composition, BMD and BMC have been repeatedly measured from 15 d up to 12 months postpartum. Other authors have performed partial studies of BMD during the first year after delivery(Reference Chan, Slater and Ronald17), beginning their study at different postpartum days(Reference Bezerra, Mendonça and Lobato18). The only longitudinal studies reported in the literature have been performed in adult women(Reference Laskey and Prentice1, Reference Kalkwarf and Specker2, Reference Affinito, Tommaselli and Di Carlo19Reference Pearson, Kaur and San24). In our study, the lack of longitudinal data from non-pregnant, non-lactating young women followed up for 12 months and from a comparative group of adult lactating women limit the interpretation of our data.

Our dietary studies showed that despite Ca intake being below recommendations(25), it was higher than the mean value observed in the National Nutrition and Health Survey(26) in non-pregnant Argentine women under 19 years old. Such low Ca intake has also been reported in other studies performed in developing and developed countries(Reference Bezerra, Mendonça and Lobato18, Reference Affinito, Tommaselli and Di Carlo19, Reference Chan, Ronald and Slater27). Other investigators have shown that nulliparous adolescents present a higher net daily Ca retention compared with adult women because they absorb more Ca from their diet, in spite of excreting more Ca in urine and faeces, and of having a higher bone turnover(Reference Weaver, Peacock and Martin28Reference Bezerra, Laboissière and King30). In our study, energy balance was negative, as evidenced by weight and fat mass loss. The marked decrease in food intake also affected Ca intake.

We observed that losses in weight, fat mass and BMI were statistically significant at 3 months postpartum, as previously published by our research group(Reference Gonzalez, Malpeli and Mansur31). Weight and lean body mass changes were similar to those reported by others in adult women(Reference Butte, Garza and Stuff32, Reference Fornes and Dorea33). Weight loss has been described in Mexican lactating adolescents, but body composition was not studied(Reference Casanueva, Marín and Gelis34). The relationship between BMD and weight has already been reported in adult pregnant(Reference Olausson, Laskey and Goldberg35, Reference Promislow, Hertz-Piccioto and Schramm36) and lactating(Reference Kulkarni, Shatrugna and Nagalla37) women and in young adults(Reference Fehily, Coles and Evans38, Reference Ho and Kung39). Our results show the association of body weight and BMI with BMD and BMC.

Adolescent mothers showed decreased BMD in the total body and at different hip sites, similar to that reported in the above-mentioned studies. Chan et al. found a higher BMD loss in the radius compared with nulliparous adolescents and adult mothers(Reference Chan, Ronald and Slater27).

BMD did not decrease in the lumbar spine and in fact a slight increase in this site was observed at 6 months postpartum, reaching 6 % above basal values at 12 months postpartum. This differs from reports by other authors, who observed BMD loss in this region in adolescents and adults(Reference Affinito, Tommaselli and Di Carlo19, Reference Sowers, Corton and Shapiro2025, Reference O’Brien, Schulman Nathanson and Mancini40).

In our population, 82 % of adolescents were still breast-feeding 12 months postpartum. In Argentina, mean annual breast feeding in low-income homes is 61·7 % (95 % CI 53·6, 69·1 %)(26). Probably our inclusion criteria (adolescent mothers exclusively breast-feeding for at least 3 months) and our careful encouragement toward breast-feeding resulted in a higher prevalence of maternal lactation 12 months postpartum. Even when most adolescents continued breast-feeding their infants, BMD recovery occurred 1 year after delivery in all sites studied except FN.

Bezerra et al. reported a statistically significant increase in total BMD after weaning(Reference Bezerra, Mendonça and Lobato18). They also found a positive correlation between BMD and time elapsed after resumption of menses (r = 0·86; P < 0·01) in adolescent mothers. Resumption of menses, connected with restoration of oestrogen levels, is associated with lower loss of bone mass during lactation. A positive correlation has been described between duration of amenorrhoea and BMD loss in adult women(Reference Kalkwarf and Specker2, Reference Ritchie, Fung and Halloran22, Reference Sowers, Hollis and Shapiro41, Reference Kolthoff, Eiken and Kristensen42). In our study, we also found that mothers who resumed menses by 3 months postpartum had higher BMD and BMC at the end of the study period.

However, a significant bone mass recovery was observed, probably due to higher efficacy for Ca retention(Reference Bailey, Martin and McKay7). It has been postulated that the lower oestrogen concentration during the first months postpartum is a key factor associated with lower action of 1,25-dihydroxyvitamin D (1,25-(OH)2D)(Reference De Santiago, Alonso and Halhali43). There is a slow but progressive increase in the concentration of 1,25-(OH)2D as lactation is prolonged(Reference King, Hallorand and Huq44). However, intestinal Ca absorption was greater in lactating mothers than in those who had resumed menses, and between 2 and 6 months post-weaning the concentration of 1,25-(OH)2D had the same increase as oestrogens in blood(Reference Hillman, Sateesha and Haussler45, Reference Wilson, Retallack and Kent46).

Since our study was focused on recovery one year postpartum, the impact of pregnancy on bone mass was not determined. In adolescent mothers followed up for a year postpartum, BMC and BMD loss and recovery follow a pattern similar to that observed in adult women(Reference Laskey and Prentice1, Reference Kalkwarf and Specker2, Reference Sowers, Corton and Shapiro2025). To our knowledge, there are no papers reporting that BMC in lactating adolescents <16 years of age is lower than that of 16–17-year-old adolescents due to the fact that the former may not be completely physiologically mature, as described in teenage pregnancies with respect to linear growth(Reference Scholl, Hediger and Ances47).

Conclusions

A significant BMD and BMC loss was observed at 6 months postpartum, with an almost total recovery at 12 months in all sites studied. Reports in similar populations with non-pregnant lactating adolescents as well as adult lactating women and control groups are needed to further support our findings.

Acknowledgements

Sources of funding: The work was supported by a grant from Universidad Iberoamericana de Mexico. Conflict of interest disclosure: None declared. Authorship responsibilities: A.M. conducted field work with adolescent mothers, participated in the design of the study, the analysis of results and the final writing of the manuscript. J.L.M. performed DEXA studies and participated in the design of the study. S.D.S. participated in the design of the study and the final writing of the manuscript. R.V. and A.A. performed field work. M.A. performed the statistical analysis of data. H.F.G. participated in the design of the study, the analysis of results and the final writing of the manuscript. Acknowledgements: The authors are grateful to Prof. Dr Fernando Viteri for a critical review of the manuscript, to the women who volunteered to take part in the study, and A. Di Maggio for manuscript editing.

References

1.Laskey, MA & Prentice, A (1999) Bone mineral changes during and after lactation. Obstet Gynecol 94, 608615.Google ScholarPubMed
2.Kalkwarf, HJ & Specker, BL (1995) Bone mineral loss during lactation and recovery after weaning. Obstet Gynecol 86, 2632.CrossRefGoogle ScholarPubMed
3.Mazzes, RB & Barden, HS (1991) Bone density in premenopausal women: effects of age, dietary intakes, physical activity, smoking and birth-control pills. Am J Clin Nutr 53, 132142.CrossRefGoogle Scholar
4.Gong, E & Heald, F (1994) Diet, nutrition and adolescence. In Modern Nutrition in Health and Disease, 8th ed., vol. 1, pp. 759767 [M Shils, J Olson and M Shike, editors]. Philadelphia, PA: Lea & Febiger.Google Scholar
5.Weaver, CM, Peacock, M, Martin, BR et al. (1997) Quantification of biochemical markers of bone turnover by kinetic measures of bone formation and resorption in young healthy females. J Bone Miner Res 12, 17141720.CrossRefGoogle ScholarPubMed
6.Forbes, GB (1976) Calcium accumulation by the human fetus. Pediatrics 57, 976977.CrossRefGoogle ScholarPubMed
7.Bailey, DA, Martin, AD, McKay, HA et al. (2000) Calcium accretion in girls and boys during puberty: a longitudinal analysis. J Bone Miner Res 15, 22452250.CrossRefGoogle ScholarPubMed
8.Laskey, MA, Prentice, A, Hanratty, LA et al. (1998) Bone changes after 3 mo of lactation: influence of calcium intake, breast-milk output, and vitamin D-receptor genotype. Am J Clin Nutr 67, 685692.CrossRefGoogle ScholarPubMed
9.Cross, NA, Hillman, LS, Allen, SH et al. (1995) Calcium homeostasis and bone metabolism during pregnancy, lactation and postweaning: a longitudinal study. Am J Clin Nutr 61, 514523.CrossRefGoogle ScholarPubMed
10.Kovacs, CS (2001) Calcium and bone metabolism in pregnancy and lactation. J Clin Endocrinol Metab 86, 23442348.Google ScholarPubMed
11.Hankin, JH (1992) Dietary intake methodology. In Research: Successful Approaches, pp. 173194 [ER Mosen, editor]. Chicago, IL: American Dietetic Association.Google Scholar
12.US Department of Agriculture (2004) USDA Food and Nutrient Database for Dietary Studies, 1.0. Beltsville, MD: USDA Agricultural Research Service, Food Surveys Research Group.Google Scholar
13.Food and Nutrition Board, National Research Council, National Academy of Sciences (1989) Recommended Dietary Allowances, 10th ed., p. 27. Washington, DC: National Academy Press.Google Scholar
14.Brunton, JA, Bayley, HS & Atkinson, SA (1993) Validation and application of dual-energy X-ray absorptiometry to measure bone mass and body composition in small infants. Am J Clin Nutr 58, 839845.CrossRefGoogle ScholarPubMed
15.Mazzes, RB, Barden, HS, Bisek, JP et al. (1990) Dual-energy X-ray absorptiometry for total-body and regional bone-mineral and soft-tissue composition. Am J Clin Nutr 51, 11061112.CrossRefGoogle Scholar
16.Ward, KA, Adams, JE & Mughal, MZ (2005) Bone status during adolescence, pregnancy and lactation. Curr Opin Obstet Gynecol 17, 435439.CrossRefGoogle ScholarPubMed
17.Chan, GM, Slater, P, Ronald, N et al. (1982) Bone mineral status of lactating mothers of different ages. Am J Obstet Gynecol 144, 438441.CrossRefGoogle ScholarPubMed
18.Bezerra, FF, Mendonça, LMC, Lobato, EC et al. (2004) Bone mass is recovered from lactation to postweaning in adolescent mothers with low calcium intakes. Am J Clin Nutr 80, 13221326.CrossRefGoogle ScholarPubMed
19.Affinito, P, Tommaselli, GA, Di Carlo, C et al. (1996) Changes in bone mineral density and calcium metabolism in breast-feeding women: a one-year follow-up study. J Clin Endocrinol Metab 81, 23142318.Google ScholarPubMed
20.Sowers, M, Corton, G, Shapiro, B et al. (1993) Changes in bone density with lactation. JAMA 269, 31303135.CrossRefGoogle ScholarPubMed
21.Polatti, F, Capuzzo, E, Viazzo, F et al. (1999) Bone mineral changes during and after lactation. Obstet Gynecol 94, 5256.Google ScholarPubMed
22.Ritchie, LD, Fung, EB, Halloran, BP et al. (1998) A longitudinal study of calcium homeostasis during human pregnancy and lactation and after resumption of menses. Am J Clin Nutr 67, 693701.CrossRefGoogle ScholarPubMed
23.Sowers, M, Randolph, J, Shapiro, B et al. (1995) A prospective study of bone density and pregnancy after an extended period of lactation with bone loss. Obstet Gynecol 85, 258259.CrossRefGoogle ScholarPubMed
24.Pearson, D, Kaur, M, San, P et al. (2002) Recovery of pregnancy mediated bone loss during lactation. Bone 34, 570578.CrossRefGoogle Scholar
25.Food and Nutrition Board, Institute of Medicine (2002) Dietary Reference Intakes 1997–2001. Washington, DC: National Academy Press.Google Scholar
26.Ministerio de Salud, Presidencia de la Nación (2007) ENNyS. Encuesta Nacional de Nutricion y Salud. Documento de Resultados 2007. http://www.msal.gov.ar/htm/site/ennys/pdf/documento_resultados_2007.pdf (accessed March 2009).Google Scholar
27.Chan, G, Ronald, N, Slater, P et al. (1982) Decreased bone mineral status in lactating adolescent mothers. J Pediatr 101, 767770.Google ScholarPubMed
28.Weaver, CM, Peacock, M, Martin, BR et al. (1996) Calcium retention estimated from indicators of skeletal status in adolescent girls and young women. Am J Clin Nutr 64, 6770.CrossRefGoogle ScholarPubMed
29.Weaver, CM, Martin, BR, Plawecki, KL et al. (1995) Differences in calcium metabolism between adolescent and adult females. Am J Clin Nutr 61, 577581.CrossRefGoogle ScholarPubMed
30.Bezerra, F, Laboissière, FP, King, JC et al. (2002) Pregnancy and lactation affect markers of calcium and bone metabolism differently in adolescent and adult women. J Nutr 132, 21832187.CrossRefGoogle ScholarPubMed
31.Gonzalez, HF, Malpeli, A, Mansur, JL et al. (2005) Changes in body composition in lactating adolescent mothers. Arch Latinoam Nutr 55, 252256.Google ScholarPubMed
32.Butte, NF, Garza, C, Stuff, JE et al. (1984) Effect of maternal diet and body composition on lactational performance. Am J Clin Nutr 39, 296306.Google ScholarPubMed
33.Fornes, NS & Dorea, JG (1995) Subcutaneous fat changes in low-income lactating mothers and growth of breast-fed infants. J Am Coll Nutr 14, 6165.CrossRefGoogle ScholarPubMed
34.Casanueva, E, Marín, A, Gelis, P et al. (1997) Changes in weight during pregnancy and lactation in adolescents. Evaluation of a nutritional intervention. Ann N Y Acad Sci 817, 353355.CrossRefGoogle Scholar
35.Olausson, H, Laskey, MA, Goldberg, GR et al. (2008) Changes in bone mineral status and bone size during pregnancy and the influences of body weight and calcium intakes. Am J Clin Nutr 88, 10321039.Google Scholar
36.Promislow, JH, Hertz-Piccioto, I, Schramm, M et al. (2004) Bed rest and other determinants of bone loss during pregnancy. Am J Obstet Gynecol 191, 10771083.CrossRefGoogle ScholarPubMed
37.Kulkarni, B, Shatrugna, V, Nagalla, B et al. (2009) Maternal weight and lean body mass may influence the lactation-related bone changes in young undernourished Indian women. Br J Nutr 101, 15271533.CrossRefGoogle ScholarPubMed
38.Fehily, AM, Coles, RJ, Evans, WD et al. (1992) Factors affecting bone density in young adults. Am J Clin Nutr 56, 579586.CrossRefGoogle ScholarPubMed
39.Ho, AY & Kung, AW (2005) Determinants of peak bone mineral density and bone area in young women. J Bone Miner Metab 23, 470475.CrossRefGoogle ScholarPubMed
40.O’Brien, K, Schulman Nathanson, M, Mancini, J et al. (2003) Calcium absorption is significantly higher in adolescents during pregnancy than in the early post partum period. Am J Clin Nutr 78, 11881193.CrossRefGoogle Scholar
41.Sowers, MF, Hollis, BW & Shapiro, B (1996) Elevated parathyroid hormone-related peptide associated with lactation and bone density loss. JAMA 276, 549554.CrossRefGoogle ScholarPubMed
42.Kolthoff, N, Eiken, P, Kristensen, B et al. (1998) Bone mineral changes during pregnancy and lactation: a longitudinal cohort study. Clin Sci 94, 405412.CrossRefGoogle ScholarPubMed
43.De Santiago, S, Alonso, L, Halhali, A et al. (2002) Negative calcium balance during lactation in rural Mexican women. Am J Clin Nutr 76, 845851.CrossRefGoogle ScholarPubMed
44.King, J, Hallorand, B, Huq, N et al. (1992) Calcium metabolism during pregnancy and lactation. In Mechanisms Regulating Lactation and Infant Nutrient Utilization, p. 135 [MF Picciano, editor]. Philadelphia, PA: Wiley-Liss.Google Scholar
45.Hillman, L, Sateesha, S, Haussler, M et al. (1981) Control of mineral homeostasis during lactation: interrelationships of 25-hydroxyvitamin D, 24,25-dihydroxyvitamin D, parathyroid hormone, calcitonin, prolactin, and estradiol. Am J Obstet Gynecol 139, 471476.CrossRefGoogle ScholarPubMed
46.Wilson, S, Retallack, R, Kent, J et al. (1990) Serum free 1,25-dihidroxyvitamin D and the free 1,25-dihidroxyvitamin D index during a longitudinal study of human pregnancy and lactation. Clin Endocrinol (Oxf) 32, 613622.CrossRefGoogle Scholar
47.Scholl, TO, Hediger, ML, Ances, IG et al. (1988) Growth during early teenage pregnancies. Lancet i, 701702.CrossRefGoogle Scholar
Figure 0

Table 1 Dietary survey results at baseline and different times postpartum: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

Figure 1

Table 2 Anthropometric parameters during the 12-month postpartum period: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

Figure 2

Fig. 1 Bone mineral density (BMD) at the different sites studied (, lumbar spine; , femur trochanter; , femoral neck; , total hip; , total body) at baseline (within 15 d after delivery) and 90, 180 and 360 d postpartum: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

Figure 3

Table 3 BMD and BMC recovery at 12 months postpartum at the different sites studied, according to resumption of menses: adolescent mothers (n 35; 17 years old or less), La Plata, Argentina

Figure 4

Fig. 2 Bone mineral content (BMC) at baseline (within 15 d after delivery) and 90, 180 and 360 d postpartum according to age (—⧫—, 14–15 years; —▪—, 16–17 years): adolescent mothers (n 35), La Plata, Argentina