Antimüllerian hormone and F2-isoprostanes in the Coronary Artery Risk Development in Young Adults (CARDIA) Study.
Antimüllerian hormone and F2-isoprostanes in the Coronary Artery Risk Development in Young Adults (CARDIA) Study.
复制标题
DOI:
10.1016/j.fertnstert.2020.04.028
复制
发表时间:
2020-09
影响因子:
6.7
通讯作者:
Wellons, Melissa F.
中科院分区:
文献类型:
--
作者:
Kim, Catherine;Slaughter, James C.;Terry, James G.;Jacobs, David R., Jr.;Parikh, Nisha;Appiah, Duke;Leader, Benjamin;Moravek, Molly B.;Wellons, Melissa F.
To examine whether F2-isoprostanes, a marker of systematic oxidative stress, are associated with anti-Müllerian hormone (AMH), an indicator of ovarian reserve, in a population-based cohort of black and white women. Cross-sectional analysis The CARDIA Women’s Study, a population-based cohort Black (n=398) and white (n=432) late reproductive-age women (mean age 40 ± 3.6 years) without histories of gynecologic surgery. Log-transformed serum AMH concentrations Linear regression models evaluated whether plasma F2-isoprostanes were associated with log-transformed AMH after adjustment for age, race, smoking, body mass index, and oral contraceptive use. Higher levels of F2-isoprostanes were associated with lower AMH levels (β−0.048 per SD, 95% confidence interval −0.087, −0.01). The observed associations were stronger at younger ages (p=0.04 for interaction between levels of age and F2-isoprostanes). Indicators of other steps in the oxidative stress pathway (super-oxide dismutase, paraoxonase activity, oxidized low-density lipoprotein cholesterol, and carotenoids) were not associated with AMH, except lower phospholipase A2 activity (β 0.036 per SD, 95% CI 0.001, 0.071) was associated with lower AMH across all ages. In a population-based cohort, higher levels of F2-isoprostanes were associated with lower ovarian reserve, particularly at younger ages. In a population-based sample, higher F2-isoprostanes, an indicator of systemic oxidative stress, is associated with lower AMH, particularly in younger women.
登录
查看更多内容
影响因子:
13.3
作者:
May-Panloup, Pascale;Boucret, Lisa;Reynier, Pascal
通讯作者:
Reynier, Pascal
影响因子:
6.1
作者:
Depmann, M.;Eijkemans, M. J. C.;Broekmans, F. J. M.
通讯作者:
Broekmans, F. J. M.
DOI:
10.1161/01.atv.0000148322.89911.44
发表时间:
2005-01-01
影响因子:
8.7
作者:
Iribarren, C;Gross, MD;Loria, CM
通讯作者:
Loria, CM
影响因子:
2.1
作者:
Lee, Keane K.;Fortmann, Stephen P.;Iribarren, Carlos
通讯作者:
Iribarren, Carlos
DOI:
10.1097/gme.0b013e3181d20cd2
发表时间:
2010-07
期刊:
Menopause (New York, N.Y.)
影响因子:
--
作者:
Appt SE;Chen H;Goode AK;Hoyer PB;Clarkson TB;Adams MR;Wilson ME;Franke AA;Kaplan JR
通讯作者:
Kaplan JR