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Birthweight and subsequent risk for thyroid and autoimmune conditions in postmenopausal women

Published online by Cambridge University Press:  18 October 2021

Brian Monahan
Affiliation:
Department of Biostatistics and Epidemiology, University of Massachusetts Amherst, Amherst, Massachusetts, USA
Leslie V. Farland
Affiliation:
Department of Epidemiology and Biostatistics, Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, Arizona, USA
Aladdin H. Shadyab
Affiliation:
Herbert Wertheim School of Public Health and Human Longevity Science, University of California, San Diego, La Jolla, California, USA
Susan E. Hankinson
Affiliation:
Department of Biostatistics and Epidemiology, University of Massachusetts Amherst, Amherst, Massachusetts, USA
JoAnn E. Manson
Affiliation:
Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA Division of Preventive Medicine, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts, USA
Cassandra N. Spracklen*
Affiliation:
Department of Biostatistics and Epidemiology, University of Massachusetts Amherst, Amherst, Massachusetts, USA
*
Address for correspondence: Cassandra N. Spracklen, Department of Biostatistics and Epidemiology, University of Massachusetts Amherst, 715 North Pleasant Street, Amherst, MA 01003, USA. Email: [email protected]

Abstract

The objective of this study was to determine the association between birthweight and risk of thyroid and autoimmune conditions in a large sample of postmenopausal women. Baseline data from the Women’s Health Initiative (n = 80,806) were used to examine the associations between birthweight category (<6 lbs., 6–7 lbs. 15 oz, 8–9 lbs. 15 oz, and ≥10 lbs.) and prevalent thyroid (underactive and overactive thyroid and goiter) and autoimmune (lupus, rheumatoid arthritis (RA), multiple sclerosis, ulcerative colitis/Crohn’s disease) conditions. Follow-up questionnaire data were used to examine the associations between birthweight and incident underactive and overactive thyroid, lupus, and RA. Logistic and Cox proportional hazards regression models were used to estimate crude and adjusted odds (OR) and hazards ratios (HR), respectively. Overall, women born weighing ≥10 lbs. had an increased risk for underactive thyroid [OR 1.14 (95% CI 1.02, 1.28)] and incident lupus [HR 1.51 (95% CI 1.12, 2.03)] and a decreased risk for overactive thyroid [OR 0.67 (95% CI 0.50, 0.92)] compared to women born weighing 6–7.99 lbs., after adjustment for adult BMI, demographic variables, and lifestyle factors. Further, women born weighing <6 lbs. were at increased risk for underactive thyroid [OR 1.13 (95% CI 1.04, 1.22)]. Birthweight was not associated with other thyroid or autoimmune disorders. High birthweight was associated with later-life thyroid and autoimmune conditions while low birthweight was associated with underactive thyroid. Preconception and prenatal interventions aimed at reducing the risk of both high and low birthweights may reduce the burden of later-life thyroid and autoimmune conditions.

Type
Original Article
Copyright
© The Author(s), 2021. Published by Cambridge University Press in association with International Society for Developmental Origins of Health and Disease

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References

Wang, L, Wang, FS, Gershwin, ME. Human autoimmune diseases: a comprehensive update. J Intern Med. 2015; 278(4), 369395. DOI 10.1111/joim.12395.CrossRefGoogle ScholarPubMed
Dinse, GE, Parks, CG, Weinberg, CR, et al. Increasing prevalence of antinuclear antibodies in the United States. Arthritis Rheumatol. 2020; 72(6), 10261035. DOI 10.1002/art.v72.6.CrossRefGoogle ScholarPubMed
Feller, M, Snel, M, Moutzouri, E, et al. Association of thyroid hormone therapy with quality of life and thyroid-related symptoms in patients with subclinical hypothyroidism: a systematic review and meta-analysis. JAMA. 2018; 320(13), 13491359. DOI 10.1001/jama.2018.13770.CrossRefGoogle ScholarPubMed
McLeod, DS, Cooper, DS. The incidence and prevalence of thyroid autoimmunity. Endocrine. 2012; 42(2), 252265. DOI 10.1007/s12020-012-9703-2.CrossRefGoogle ScholarPubMed
Antonelli, A, Ferrari, SM, Corrado, A, Di Domenicantonio, A, Fallahi, P. Autoimmune thyroid disorders. Autoimmun Rev. 2015; 14(2), 174180. DOI 10.1016/j.autrev.2014.10.016.CrossRefGoogle ScholarPubMed
Conigliaro, P, DʼAntonio, A, Pinto, S, et al. Autoimmune thyroid disorders and rheumatoid arthritis: a bidirectional interplay. Autoimmun Rev. 2020; 19(6), 102529. DOI 10.1016/j.autrev.2020.102529.CrossRefGoogle ScholarPubMed
Ortona, E, Pierdominici, M, Maselli, A, Veroni, C, Aloisi, F, Shoenfeld, Y. Sex-based differences in autoimmune diseases. Ann Ist Super Sanita. 2016; 52, 205212. DOI 10.4415/ann_16_02_12.Google ScholarPubMed
Bel Lassen, P, Kyrilli, A, Lytrivi, M, Corvilain, B. Gravesʼ disease, multinodular goiter and subclinical hyperthyroidism. Ann Endocrinol (Paris). 2019; 80(4), 240249. DOI 10.1016/j.ando.2018.09.004.CrossRefGoogle ScholarPubMed
De Leo, S, Lee, SY, Braverman, LE. Hyperthyroidism. Lancet. 2016; 388(10047), 906918. DOI 10.1016/s0140-6736(16)00278-6.CrossRefGoogle ScholarPubMed
Rees, F, Doherty, M, Grainge, M, Davenport, G, Lanyon, P, Zhang, W. The incidence and prevalence of systemic lupus erythematosus in the UK, 1999-2012. Ann Rheum Dis. 2016; 75(1), 136141. DOI 10.1136/annrheumdis-2014-206334.CrossRefGoogle Scholar
Barker, DJ. The developmental origins of adult disease. J Am Coll Nutr. 2004; 23(sup6), 588S595S.CrossRefGoogle ScholarPubMed
Ryckman, KK, Rillamas-Sun, E, Spracklen, CN, et al. Ethnic differences in the relationship between birth weight and type 2 diabetes mellitus in postmenopausal women. Diabetes Metab. 2014; 40(5), 379385. DOI 10.1016/j.diabet.2014.03.003.CrossRefGoogle ScholarPubMed
Smith, CJ, Ryckman, KK, Barnabei, VM, et al. The impact of birth weight on cardiovascular disease risk in the Women’s Health Initiative. Nutr Metab Cardiovasc Dis. 2016; 26, 239245. DOI 10.1016/j.numecd.2015.10.015.CrossRefGoogle ScholarPubMed
Spracklen, CN, Ryckman, KK, Robinson, JG, et al. Low birth weight and risk of later-life physical disability in women. J Gerontol A Biol Sci Med Sci. 2017; 72, 543547. DOI 10.1093/gerona/glw134.Google ScholarPubMed
Spracklen, CN, Wallace, RB, Sealy-Jefferson, S, et al. Birth weight and subsequent risk of cancer. Cancer Epidemiol. 2014; 38(5), 538543. DOI 10.1016/j.canep.2014.07.004.CrossRefGoogle ScholarPubMed
Chandran, U, Demissie, K, Echeverria, SE, Long, JB, Mizan, S, Mino, J. Food allergy among low birthweight children in a national survey. Matern Child Health J. 2013; 17(1), 165171. DOI 10.1007/s10995-012-0960-8.CrossRefGoogle ScholarPubMed
Xu, X-F, Li, Y-J, Sheng, Y-J, Liu, J-L, Tang, L-F, Chen, Z-M. Effect of low birth weight on childhood asthma: a meta-analysis. BMC Pediatr. 2014; 14(1), 275. DOI 10.1186/1471-2431-14-275.CrossRefGoogle ScholarPubMed
Brix, TH, Kyvik, KO, Hegedüs, L. Low birth weight is not associated with clinically overt thyroid disease: a population based twin case-control study. Clin Endocrinol. 2000; 53(2), 171176. DOI 10.1046/j.1365-2265.2000.01025.x.CrossRefGoogle Scholar
Kajantie, E, Phillips, DIW, Osmond, C, Barker, DJP, Forsén, T, Eriksson, JG. Spontaneous hypothyroidism in adult women is predicted by small body size at birth and during childhood. J Clin Endocr Metab. 2006; 91(12), 49534956. DOI 10.1210/jc.2006-1093.CrossRefGoogle ScholarPubMed
Mandl, LA, Costenbader, KH, Simard, JF, Karlson, EW. Is birthweight associated with risk of rheumatoid arthritis? Data from a large cohort study. Ann Rheum Dis. 2009; 68(4), 514518. DOI 10.1136/ard.2007.080937.CrossRefGoogle ScholarPubMed
Parks, CG, DʼAloisio, AA, Sandler, DP. Early life factors associated with adult-onset systemic lupus erythematosus in women. Front Immunol. 2016; 7(Suppl 1), 103. DOI 10.3389/fimmu.2016.00103.CrossRefGoogle ScholarPubMed
Desai, MK, Brinton, RD. Autoimmune disease in women: endocrine transition and risk across the lifespan. Front Endocrinol. 2019; 10, 265. DOI 10.3389/fendo.2019.00265.CrossRefGoogle ScholarPubMed
Anderson, GL, Manson, J, Wallace, R, et al. Implementation of the Women’s Health Initiative study design. Ann Epidemiol. 2003; 13(9), S5S17.CrossRefGoogle ScholarPubMed
Manson, JAE, Chlebowski, RT, Stefanick, ML, et al. Menopausal hormone therapy and health outcomes during the intervention and extended poststopping phases of the Women’s Health Initiative randomized trials. JAMA. 2013; 310(13), 13531368. DOI 10.1001/jama.2013.278040.CrossRefGoogle ScholarPubMed
Prentice, RL, Anderson, GL. The women’s health initiative: lessons learned. Annu Rev Public Health. 2008; 29(1), 131150. DOI 10.1146/annurev.publhealth.29.020907.090947.CrossRefGoogle ScholarPubMed
Troy, LM, Michels, KB, Hunter, DJ, et al. Self-reported birthweight and history of having been breastfed among younger women: an assessment of validity. Int J Epidemiol. 1996; 25(1), 122127. DOI 10.1093/ije/25.1.122.CrossRefGoogle Scholar
Walitt, BT, Constantinescu, F, Katz, JD, et al. Validation of self-report of rheumatoid arthritis and systemic lupus erythematosus: the Women’s Health Initiative. J Rheumatol. 2008; 35, 811818.Google ScholarPubMed
Johnson, W, Choh, AC, Soloway, LE, Czerwinski, SA, Towne, B, Demerath, EW. Eighty-year trends in infant weight and length growth: the Fels Longitudinal Study. J Pediatr. 2012; 160(5), 762768. DOI 10.1016/j.jpeds.2011.11.002.CrossRefGoogle ScholarPubMed
Costenbader, KH, Karlson, EW. Cigarette smoking and autoimmune disease: what can we learn from epidemiology? Lupus. 2006; 15(11), 737745. DOI 10.1177/0961203306069344.CrossRefGoogle ScholarPubMed
Farland, LV, Correia, KFB, Dodge, LE, et al. The importance of mediation in reproductive health studies. Hum Reprod. 2020; 35(6), 12621266. DOI 10.1093/humrep/deaa064.CrossRefGoogle ScholarPubMed
Tu, YK, West, R, Ellison, GT, Gilthorpe, MS. Why evidence for the fetal origins of adult disease might be a statistical artifact: the "reversal paradox" for the relation between birth weight and blood pressure in later life. Am J Epidemiol. 2005; 161(1), 2732. DOI 10.1093/aje/kwi002.CrossRefGoogle ScholarPubMed
Santin, AP, Furlanetto, TW. Role of estrogen in thyroid function and growth regulation. J Thyroid Res. 2011; 2011, 875125. DOI 10.4061/2011/875125.CrossRefGoogle ScholarPubMed
Korada, M, Pearce, MS, Avis, E, Turner, S, Cheetham, T. TSH levels in relation to gestation, birth weight and sex. Horm Res. 2009; 72(2), 120123. DOI 10.1159/000232165.Google ScholarPubMed
Korevaar, TIM, Chaker, L, Jaddoe, VWV, Visser, TJ, Medici, M, Peeters, RP. Maternal and birth characteristics are determinants of offspring thyroid function. J Clin Endocr Metab. 2016; 101(1), 206213. DOI 10.1210/jc.2015-3559.CrossRefGoogle ScholarPubMed
Frost, M, Petersen, I, Hegedüs, L, Christiansen, L, Brix, T, Christensen, K. Regulation of the pituitary-thyroid axis in adulthood is not related to birth weight: evidence from extremely birth weight-discordant monozygotic Danish twin pairs. Thyroid. 2013; 23(7), 785790. DOI 10.1089/thy.2012.0095.CrossRefGoogle Scholar
Phillips, DI, Barker, DJ, Osmond, C. Infant feeding, fetal growth and adult thyroid function. Acta Endocrinol. 1993; 129(2), 134138. DOI 10.1530/acta.0.1290134.CrossRefGoogle ScholarPubMed
Phillips, DI, Cooper, C, Fall, C, et al. Fetal growth and autoimmune thyroid disease. Q J Med. 1993; 86, 247253.Google ScholarPubMed
Brix, TH, Hansen, PS, Rudbeck, AB, et al. Low birth weight is not associated with thyroid autoimmunity: a population-based twin study. J Clin Endocr Metab. 2006; 91(9), 34993502. DOI 10.1210/jc.2006-1348.CrossRefGoogle Scholar
Hashemipour, M, Hovsepian, S, Ansari, A, Keikha, M, Khalighinejad, P, Niknam, N. Screening of congenital hypothyroidism in preterm, low birth weight and very low birth weight neonates: a systematic review. Pediatr Neonatol. 2018; 59(1), 314. DOI 10.1016/j.pedneo.2017.04.006.CrossRefGoogle ScholarPubMed
Zhou, J, Luo, J, Lin, J, et al. Perinatal risk factors for congenital hypothyroidism: a retrospective cohort study performed at a tertiary hospital in China. Medicine. 2020; 99(26), e20838. DOI 10.1097/md.0000000000020838.CrossRefGoogle Scholar
Franco, B, Laura, F, Sara, N, Salvatore, G. Thyroid function in small for gestational age newborns: a review. J Clin Res Pediatr Endocrinol. 2013; 5(Suppl 1), 27. DOI 10.4274/jcrpe.846.Google ScholarPubMed
Carlens, C, Jacobsson, L, Brandt, L, Cnattingius, S, Stephansson, O, Askling, J. Perinatal characteristics, early life infections and later risk of rheumatoid arthritis and juvenile idiopathic arthritis. Ann Rheum Dis. 2009; 68(7), 11591164. DOI 10.1136/ard.2008.089342.CrossRefGoogle ScholarPubMed
Parks, CG, DʼAloisio, AA, DeRoo, LA, et al. Childhood socioeconomic factors and perinatal characteristics influence development of rheumatoid arthritis in adulthood. Ann Rheum Dis. 2013; 72(3), 350356. DOI 10.1136/annrheumdis-2011-201083.CrossRefGoogle ScholarPubMed
Svendsen, AJ, Kyvik, KO, Houen, G, et al. Newborn infant characteristics and risk of future rheumatoid arthritis: a twin-control study. Rheumatol Int. 2014; 34(4), 523528. DOI 10.1007/s00296-013-2886-x.CrossRefGoogle ScholarPubMed
Gardener, H, Munger, KL, Chitnis, T, Michels, KB, Spiegelman, D, Ascherio, A. Prenatal and perinatal factors and risk of multiple sclerosis. Epidemiology. 2009; 20(4), 611618. DOI 10.1097/EDE.0b013e31819ed4b9.CrossRefGoogle ScholarPubMed
Ramagopalan, SV, Valdar, W, Dyment, DA, et al. No effect of preterm birth on the risk of multiple sclerosis: a population based study. BMC Neurol. 2008; 8(1), 30. DOI 10.1186/1471-2377-8-30.CrossRefGoogle ScholarPubMed
Luetic, GG, Menichini, ML, Deri, N, et al. High birth weight and risk of multiple sclerosis: a multicentre study in Argentina. Mult Scler Relat Disord. 2021; 47(6), 102628. DOI 10.1016/j.msard.2020.102628.CrossRefGoogle ScholarPubMed
Arkema, EV, Simard, JF. Perinatal risk factors for future SLE: a population-based nested case-control study. Lupus. 2015; 24(8), 869874. DOI 10.1177/0961203315570160.CrossRefGoogle ScholarPubMed
Coleman, L A, Naleway, A L, Davis, M E, Greenlee, R T, Wilson, D, McCarty, D J. Birth weight and systemic lupus erythematosus. Lupus. 2005; 14(7), 526528. DOI 10.1191/0961203305lu2152oa.CrossRefGoogle ScholarPubMed
Simard, JF, Karlson, EW, Costenbader, KH, et al. Perinatal factors and adult-onset lupus. Arthritis Rheum. 2008; 59(8), 11551161. DOI 10.1002/art.23930.CrossRefGoogle ScholarPubMed
Khalili, H, Ananthakrishnan, AN, Higuchi, LM, Richter, JM, Fuchs, CS, Chan, AT. Early life factors and risk of inflammatory bowel disease in adulthood. Inflamm Bowel Dis. 2013; 19(3), 542547. DOI 10.1097/MIB.0b013e31828132f8.CrossRefGoogle ScholarPubMed
Mendall, M, Jensen, CB, Ängquist, LH, Baker, JL, Jess, T. Childhood growth and risk of inflammatory bowel disease: a population-based study of 317,030 children. Scand J Gastroenterol. 2019; 54(7), 863868. DOI 10.1080/00365521.2019.1635201.CrossRefGoogle ScholarPubMed
Class, QA, Rickert, ME, Lichtenstein, P, DʼOnofrio, BM. Birth weight, physical morbidity, and mortality: a population-based sibling-comparison study. Am J Epidemiol. 2014; 179(5), 550558. DOI 10.1093/aje/kwt304.CrossRefGoogle ScholarPubMed
Ward, AM, Syddall, HE, Wood, PJ, Chrousos, GP, Phillips, DI. Fetal programming of the hypothalamic-pituitary-adrenal (HPA) axis: low birth weight and central HPA regulation. J Clin Endocr Metab. 2004; 89(3), 12271233. DOI 10.1210/jc.2003-030978.CrossRefGoogle ScholarPubMed
Imrich, R. The role of neuroendocrine system in the pathogenesis of rheumatic diseases (minireview). Endocr Regul. 2002; 36, 95106.Google Scholar
Gutiérrez, MA, Garcia, ME, Rodriguez, JA, Rivero, S, Jacobelli, S. Hypothalamic-pituitary-adrenal axis function and prolactin secretion in systemic lupus erythematosus. Lupus. 1998; 7(6), 404408. DOI 10.1191/096120398678920343.CrossRefGoogle ScholarPubMed
Gold, SM, Mohr, DC, Huitinga, I, Flachenecker, P, Sternberg, EM, Heesen, C. The role of stress-response systems for the pathogenesis and progression of MS. Trends Immunol. 2005; 26(12), 644652. DOI 10.1016/j.it.2005.09.010.CrossRefGoogle ScholarPubMed
Stasi, C, Orlandelli, E. Role of the brain-gut axis in the pathophysiology of Crohn’s disease. Dig Dis. 2008; 26(2), 156166. DOI 10.1159/000116774.CrossRefGoogle ScholarPubMed
Kc, K, Shakya, S, Zhang, H. Gestational diabetes mellitus and macrosomia: a literature review. Ann Nutr Metab. 2015; 66(Suppl. 2), 1420. DOI 10.1159/000371628.CrossRefGoogle ScholarPubMed
Regnault, TR, Nijland, MJ, Budge, H, Morrison, JL. Basic experimental and clinical advances in the mechanisms underlying abnormal pregnancy outcomes. J Pregnancy. 2013; 2013, 327638. DOI 10.1155/2013/327638.CrossRefGoogle ScholarPubMed
Phillips, D. Endocrine programming and fetal origins of adult disease. Trends Endocrinol Metab. 2002; 13(9), 363. DOI 10.1016/s1043-2760(02)00696-3.CrossRefGoogle ScholarPubMed
Jaworowicz, DJ, Nie, J, Bonner, MR, et al. Agreement between self-reported birth weight and birth certificate weights. J Dev Orig Health Dis. 2010; 1(2), 106113. DOI 10.1017/S2040174410000012.CrossRefGoogle ScholarPubMed
Wodskou, PM, Hundrup, YA, Obel, EB, Jorgensen, T. Validity of self-reported birthweight among middle-aged and elderly women in the Danish Nurse Cohort Study. Acta Obstet Gyn Scan. 2010; 89(9), 11341139. DOI 10.3109/00016349.2010.500370.CrossRefGoogle ScholarPubMed
American Thyroid Associaiton. American Thyroid Associaiton General Inforamtion/Press Room. 2021. https://www.thyroid.org/media-main/press-room/.Google Scholar
Leung, AM, Braverman, LE. Consequences of excess iodine. Nat Rev Endocrinol. 2014; 10(3), 136142. DOI 10.1038/nrendo.2013.251.CrossRefGoogle ScholarPubMed
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