Show simple item record

Cumulative Endogenous Estrogen Exposure Is Associated With Postmenopausal Fracture Risk: The Women’s Health Initiative Study

dc.contributor.authorLeBlanc, Erin S
dc.contributor.authorHovey, Kathleen M
dc.contributor.authorCauley, Jane A
dc.contributor.authorStefanick, Marcia
dc.contributor.authorPeragallo, Rachel
dc.contributor.authorNaughton, Michelle J
dc.contributor.authorAndrews, Christopher A
dc.contributor.authorCrandall, Carolyn J
dc.date.accessioned2022-08-02T18:57:55Z
dc.date.available2023-08-02 14:57:53en
dc.date.available2022-08-02T18:57:55Z
dc.date.issued2022-07
dc.identifier.citationLeBlanc, Erin S; Hovey, Kathleen M; Cauley, Jane A; Stefanick, Marcia; Peragallo, Rachel; Naughton, Michelle J; Andrews, Christopher A; Crandall, Carolyn J (2022). "Cumulative Endogenous Estrogen Exposure Is Associated With Postmenopausal Fracture Risk: The Women’s Health Initiative Study." Journal of Bone and Mineral Research 37(7): 1260-1269.
dc.identifier.issn0884-0431
dc.identifier.issn1523-4681
dc.identifier.urihttps://hdl.handle.net/2027.42/173119
dc.description.abstractWe aimed to evaluate the relationship between cumulative endogenous estrogen exposure and fracture risk in 150,682 postmenopausal women (aged 50 to 79 years at baseline) who participated in the Women’s Health Initiative. We hypothesized that characteristics indicating lower cumulative endogenous estrogen exposure would be associated with increased fracture risk. We determined ages at menarche and menopause as well as history of irregular menses from baseline questionnaires and calculated years of endogenous estrogen exposure from ages at menarche and menopause. Incident clinical fractures were self-reported over an average 16.7 years of follow-up. We used multivariable proportional hazards models to assess the associations between the estrogen-related variables and incidence of any clinical fracture. In fully adjusted models, those with the fewest years of endogenous estrogen exposure (<30) had an 11% higher risk of developing central body fractures and a 9% higher risk of lower extremity fractures than women with 36 to 40 years of endogenous estrogen exposure (the reference category). In contrast, women with the most years of endogenous estrogen exposure (more than 45 years) had a 9% lower risk of lower extremity fractures than the reference category. Women with irregular (not monthly) menstrual cycles were 7% to 8% more likely to experience lower extremity fractures than women with regular monthly cycles. Our findings support the hypothesis that characteristics signifying lower cumulative endogenous estrogen exposure are associated with higher fracture risk. © 2022 American Society for Bone and Mineral Research (ASBMR).
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.otherMENARCHE
dc.subject.otherFRACTURE
dc.subject.otherMENOPAUSE
dc.subject.otherIRREGULAR MENSES
dc.titleCumulative Endogenous Estrogen Exposure Is Associated With Postmenopausal Fracture Risk: The Women’s Health Initiative Study
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelInternal Medicine and Specialities
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/173119/1/jbmr4613_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/173119/2/jbmr4613.pdf
dc.identifier.doi10.1002/jbmr.4613
dc.identifier.sourceJournal of Bone and Mineral Research
dc.identifier.citedreferenceWalsh LJ, Lewis SA, Wong CA, et al. The impact of oral corticosteroid use on bone mineral density and vertebral fracture. Am J Respir Crit Care Med. 2002; 166 ( 5 ): 691 - 695.
dc.identifier.citedreferenceAnderson GL, Manson J, Wallace R, et al. Implementation of the Women’s Health Initiative study design. Ann Epidemiol. 2003; 13 ( 9 Suppl ): S5 - S17.
dc.identifier.citedreferenceHays J, Hunt JR, Hubbell FA, et al. The Women’s Health Initiative recruitment methods and results. Ann Epidemiol. 2003; 13 ( 9 Suppl ): S18 - S77.
dc.identifier.citedreferenceRossouw JE, Prentice RL, Manson JE, et al. Postmenopausal hormone therapy and risk of cardiovascular disease by age and years since menopause. JAMA. 2007; 297 ( 13 ): 1465 - 1477.
dc.identifier.citedreferenceLeBlanc ES, Kapphahn K, Hedlin H, et al. Reproductive history and risk of type 2 diabetes mellitus in postmenopausal women: findings from the Women’s Health Initiative. Menopause. 2017; 24 ( 1 ): 64 - 72.
dc.identifier.citedreferenceLey SH, Li Y, Tobias DK, et al. Duration of reproductive life span, age at menarche, and age at menopause are associated with risk of cardiovascular disease in women. J Am Heart Assoc. 2017; 6 ( 11 ): e006713.
dc.identifier.citedreferenceWeinstein M, Gorrindo T, Riley A, et al. Timing of menopause and patterns of menstrual bleeding. Am J Epidemiol. 2003; 158 ( 8 ): 782 - 791.
dc.identifier.citedreferenceYermachenko A, Dvornyk V. Nongenetic determinants of age at menarche: a systematic review. Biomed Res Int. 2014; 2014: 371583.
dc.identifier.citedreferenceMcKinlay SM, Brambilla DJ, Posner JG. The normal menopause transition. Maturitas. 1992; 14 ( 2 ): 103 - 115.
dc.identifier.citedreferenceChao S. The effect of lactation on ovulation and fertility. Clin Perinatol. 1987; 14 ( 1 ): 39 - 50.
dc.identifier.citedreferenceHays RD, Sherbourne CD, Mazel RM. The RAND 36-item health survey 1.0. Health Econ. 1993; 2 ( 3 ): 217 - 227.
dc.identifier.citedreferenceRankin K, Bove R. Caring for women with multiple sclerosis across the lifespan. Curr Neurol Neurosci Rep. 2018; 18 ( 7 ): 36.
dc.identifier.citedreferenceKusters CDJ, Paul KC, Duarte Folle A, et al. Increased menopausal age reduces the risk of Parkinson’s disease: a Mendelian randomization approach. Mov Disord. 2021; 36 ( 10 ): 2264 - 2272.
dc.identifier.citedreferenceHall PS, Nah G, Howard BV, et al. Reproductive factors and incidence of heart failure hospitalization in the Women’s Health Initiative. J Am Coll Cardiol. 2017; 69 ( 20 ): 2517 - 2526.
dc.identifier.citedreferenceLim JH, Kang D, Hong YS, et al. Association between reproductive lifespan and lung function among postmenopausal women. J Thorac Dis. 2020; 12 ( 8 ): 4243 - 4252.
dc.identifier.citedreferenceDennison EM, Compston JE, Flahive J, et al. Effect of co-morbidities on fracture risk: findings from the Global Longitudinal Study of Osteoporosis in Women (GLOW). Bone. 2012; 50 ( 6 ): 1288 - 1293.
dc.identifier.citedreferenceViswanathan M, Reddy S, Berkman N, et al. Screening to prevent osteoporotic fractures: updated evidence report and systematic review for the US Preventive Services Task Force. JAMA. 2018; 319 ( 24 ): 2532 – 51.
dc.identifier.citedreferenceMerlijn T, Swart KMA, van der Horst HE, Netelenbos JC, Elders PJM. Fracture prevention by screening for high fracture risk: a systematic review and meta-analysis. Osteoporos Int. 2020; 31 ( 2 ): 251 - 257.
dc.identifier.citedreferenceMcCormick DP, Ponder SW, Fawcett HD, Palmer JL. Spinal bone mineral density in 335 normal and obese children and adolescents: evidence for ethnic and sex differences. J Bone Miner Res. 1991; 6 ( 5 ): 507 - 513.
dc.identifier.citedreferenceOtt SM. Bone density in adolescents. N Engl J Med. 1991; 325 ( 23 ): 1646 - 1647.
dc.identifier.citedreferenceSvejme O, Ahlborg HG, Nilsson J, Karlsson MK. Early menopause and risk of osteoporosis, fracture and mortality: a 34-year prospective observational study in 390 women. BJOG. 2012; 119 ( 7 ): 810 - 816.
dc.identifier.citedreferenceHarlow SD, Ephross SA. Epidemiology of menstruation and its relevance to women’s health. Epidemiol Rev. 1995; 17 ( 2 ): 265 - 286.
dc.identifier.citedreferenceChen Z, Kooperberg C, Pettinger MB, et al. Validity of self-report for fractures among a multiethnic cohort of postmenopausal women: results from the Women’s Health Initiative observational study and clinical trials. Menopause. 2004; 11 ( 3 ): 264 - 274.
dc.identifier.citedreferenceColditz GA, Stampfer MJ, Willett WC, et al. Reproducibility and validity of self-reported menopausal status in a prospective cohort study. Am J Epidemiol. 1987; 126 ( 2 ): 319 - 325.
dc.identifier.citedreferenceden Tonkelaar I. Validity and reproducibility of self-reported age at menopause in women participating in the DOM-project. Maturitas. 1997; 27 ( 2 ): 117 - 123.
dc.identifier.citedreferenceLundblad MW, Jacobsen BK. The reproducibility of self-reported age at menarche: the Tromsø study. BMC Womens Health. 2017; 17 ( 1 ): 62.
dc.identifier.citedreferenceCooper R, Blell M, Hardy R, et al. Validity of age at menarche self-reported in adulthood. J Epidemiol Community Health. 2006; 60 ( 11 ): 993 - 997.
dc.identifier.citedreferenceClarke BL, Khosla S. Female reproductive system and bone. Arch Biochem Biophys. 2010; 503 ( 1 ): 118 - 128.
dc.identifier.citedreferencePaganini-Hill A, Atchison KA, Gornbein JA, Nattiv A, Service SK, White SC. Menstrual and reproductive factors and fracture risk: the Leisure World Cohort Study. J Womens Health (Larchmt). 2005; 14 ( 9 ): 808 - 819.
dc.identifier.citedreferenceCooper GS, Sandler DP. Long-term effects of reproductive-age menstrual cycle patterns on peri- and postmenopausal fracture risk. Am J Epidemiol. 1997; 145 ( 9 ): 804 - 809.
dc.identifier.citedreferenceNicodemus KK, Folsom AR, Anderson KE. Menstrual history and risk of hip fractures in postmenopausal women. The Iowa Women’s Health Study. Am J Epidemiol. 2001; 153 ( 3 ): 251 - 255.
dc.identifier.citedreferenceNguyen TV, Jones G, Sambrook PN, White CP, Kelly PJ, Eisman JA. Effects of estrogen exposure and reproductive factors on bone mineral density and osteoporotic fractures. J Clin Endocrinol Metab. 1995; 80 ( 9 ): 2709 - 2714.
dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.