Please use this identifier to cite or link to this item: https://doi.org/10.1136/bmjdrc-2020-001951
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dc.titleCross-sectional and prospective relationships of endogenous progestogens and estrogens with glucose metabolism in men and women: A KORA F4/FF4 Study
dc.contributor.authorLau, Lina Hui Ying
dc.contributor.authorNano, Jana
dc.contributor.authorCecil, Alexander
dc.contributor.authorSchederecker, Florian
dc.contributor.authorRathmann, Wolfgang
dc.contributor.authorPrehn, Cornelia
dc.contributor.authorZeller, Tanja
dc.contributor.authorLechner, Andreas
dc.contributor.authorAdamski, Jerzy
dc.contributor.authorPeters, Annette
dc.contributor.authorThorand, Barbara
dc.date.accessioned2022-10-13T07:55:08Z
dc.date.available2022-10-13T07:55:08Z
dc.date.issued2021-02-01
dc.identifier.citationLau, Lina Hui Ying, Nano, Jana, Cecil, Alexander, Schederecker, Florian, Rathmann, Wolfgang, Prehn, Cornelia, Zeller, Tanja, Lechner, Andreas, Adamski, Jerzy, Peters, Annette, Thorand, Barbara (2021-02-01). Cross-sectional and prospective relationships of endogenous progestogens and estrogens with glucose metabolism in men and women: A KORA F4/FF4 Study. BMJ Open Diabetes Research and Care 9 (1) : e001951. ScholarBank@NUS Repository. https://doi.org/10.1136/bmjdrc-2020-001951
dc.identifier.issn2052-4897
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/233237
dc.description.abstractIntroduction Relationships between endogenous female sex hormones and glycemic traits remain understudied, especially in men. We examined whether endogenous 17?-hydroxyprogesterone (17-OHP), progesterone, estradiol (E2), and free estradiol (fE2) were associated with glycemic traits and glycemic deterioration. Research design and methods 921 mainly middle-aged and elderly men and 390 perimenopausal/postmenopausal women from the German population-based Cooperative Health Research in the Region of Augsburg (KORA) F4/FF4 cohort study were followed up for a median of 6.4 years. Sex hormones were measured at baseline using mass spectrometry. We calculated regression coefficients (?) and ORs with 95% CIs using multivariable-adjusted linear and logistic regression models for Z-standardized hormones and glycemic traits or glycemic deterioration (ie, worsening of categorized glucose tolerance status), respectively. Results In the cross-sectional analysis (n=1222 men and n=594 women), in men, 17-OHP was inversely associated with 2h-glucose (2hG) (?=-0.067, 95% CI-0.120 to-0.013) and fasting insulin (?=-0.074, 95% CI-0.118 to-0.030), and positively associated with Quantitative Insulin Sensitivity Check Index (QUICKI) (?=0.061, 95% CI 0.018 to 0.105). Progesterone was inversely associated with fasting insulin (?=-0.047, 95% CI-0.088 to-0.006) and positively associated with QUICKI (?=0.041, 95% CI 0.001 to 0.082). E2 was inversely associated with fasting insulin (?=-0.068, 95% CI-0.116 to-0.020) and positively associated with QUICKI (?=0.059, 95% CI 0.012 to 0.107). fE2 was positively associated with glycated hemoglobin (HbA 1c) (?=0.079, 95% CI 0.027 to 0.132). In women, 17-OHP was positively associated with fasting glucose (FG) (?=0.068, 95% CI 0.014 to 0.123). fE2 was positively associated with FG (?=0.080, 95% CI 0.020 to 0.141) and HbA 1c (?=0.121, 95% CI 0.062 to 0.180). In the sensitivity analyses restricted to postmenopausal women, we observed a positive association between 17-OHP and glycemic deterioration (OR=1.518, 95% CI 1.033 to 2.264). Conclusions Inter-relations exist between female sex hormones and glucose-related traits among perimenopausal/postmenopausal women and insulin-related traits among men. Endogenous progestogens and estrogens appear to be involved in glucose homeostasis not only in women but in men as well. Further well-powered studies assessing causal associations between endogenous female sex hormones and glycemic traits are warranted. © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY. Published by BMJ.
dc.publisherBMJ Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectDiabetes mellitus
dc.subjectEstrogens
dc.subjectProgesterone
dc.typeArticle
dc.contributor.departmentBIOCHEMISTRY
dc.description.doi10.1136/bmjdrc-2020-001951
dc.description.sourcetitleBMJ Open Diabetes Research and Care
dc.description.volume9
dc.description.issue1
dc.description.pagee001951
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