Literature DB >> 20843950

Longitudinal study of insulin resistance and sex hormones over the menstrual cycle: the BioCycle Study.

Edwina H Yeung1, Cuilin Zhang, Sunni L Mumford, Aijun Ye, Maurizio Trevisan, Liwei Chen, Richard W Browne, Jean Wactawski-Wende, Enrique F Schisterman.   

Abstract

CONTEXT: Conflicting findings have been reported regarding the effect of menstrual cycle phase and sex hormones on insulin sensitivity.
OBJECTIVE: The aim was to determine the pattern of insulin resistance over the menstrual cycle and whether variations in sex hormones explain these patterns.
DESIGN: The BioCycle study is a longitudinal study that measured hormones at different phases of the menstrual cycle. Participants had up to eight visits per cycle; each visit was timed using fertility monitors to capture sensitive windows of hormonal changes.
SETTING: The study was conducted in the general community of the University at Buffalo (Buffalo, NY). PARTICIPANTS: A total of 257 healthy, premenopausal women (age, 27±8 yr; body mass index, 24±4 kg/m2) participated in the study. MAIN OUTCOME MEASURES: We measured fasting insulin, glucose, and insulin resistance by the homeostasis model of insulin resistance (HOMA-IR).
RESULTS: Significant changes in HOMA-IR were observed over the menstrual cycle; from a midfollicular phase level of 1.35, levels rose to 1.59 during the early luteal phase and decreased to 1.55 in the late-luteal phase. HOMA-IR levels primarily reflected changes in insulin and not glucose. After adjustment for age, race, cycle, and other sex hormones, HOMA-IR was positively associated with estradiol (β=0.082; P<0.001) and progesterone (β=0.025; P<0.001), and inversely associated with FSH (adjusted β=-0.040; P<0.001) and SHBG (β=-0.085; P<0.001). LH was not associated with HOMA-IR. Further adjustment for BMI weakened the association with SHBG (β=-0.057; P=0.06) but did not affect other associations.
CONCLUSION: Insulin exhibited minor menstrual cycle variability. Estradiol and progesterone were positively associated with insulin resistance and should be considered in studies of insulin resistance among premenopausal women.

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Year:  2010        PMID: 20843950      PMCID: PMC2999972          DOI: 10.1210/jc.2010-0702

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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