TY - JOUR
T1 - Antimullerian Hormone, a Marker of Ovarian Reserve, Is Protective Against Presence and Severity of NASH in Premenopausal Women
AU - Maldonado, Stephanie S.
AU - Cedars, Marcelle I.
AU - Yates, Katherine P.
AU - Wilson, Laura A.
AU - Gill, Ryan
AU - Terrault, Norah A.
AU - Suzuki, Ayako
AU - Sarkar, Monika A.
N1 - Publisher Copyright:
© 2024 AGA Institute
PY - 2024/2
Y1 - 2024/2
N2 - Background & Aims: Antimüllerian hormone (AMH) is a marker of ovarian reserve with emerging data linking lower levels to some metabolic and inflammatory diseases in women. Whether AMH levels influence nonalcoholic fatty liver disease (NAFLD) is unknown. Methods: Leveraging the NASH Clinical Research Network we determined the association of AMH levels within 6 months of liver biopsy with presence and severity of histologic measures of NAFLD in premenopausal women. Outcomes included presence of nonalcoholic steatohepatitis (NASH), presence and severity of fibrosis, and NAFLD Activity Score and its components. Logistic and ordinal logistic regression models were adjusted for age, race/ethnicity, homeostatic model assessment for insulin resistance, body mass index, dyslipidemia, polycystic ovary syndrome, estrogen-progestin use, and menstrual cyclicity. Results: Median cohort age was 35 years; 73% were white and 24% Hispanic. Thirty-three percent had diabetes, 81% had obesity, and 95% had dyslipidemia. On biopsy 71% had NASH, 68% had any fibrosis, and 15% had advanced fibrosis. On adjusted analysis (n = 205), higher AMH quartiles were inversely associated with NAFLD histology including prevalent NASH (adjusted odds ratio [AOR], 0.64; 95% confidence interval [CI], 0.41–1.00), NAFLD Activity Score ≥5 (AOR, 0.52; 95% CI, 0.35–0.77), Mallory hyaline (AOR, 0.54; 95% CI, 0.35–0.82), and higher fibrosis stage (AOR, 0.70; 95% CI, 0.51–0.98). The protective effects of AMH were more pronounced among women without polycystic ovary syndrome (n = 164), including lower odds of NASH (AOR, 0.53; 95% CI, 0.32–0.90) and any NASH fibrosis (AOR, 0.54; 95% CI, 0.32–0.93). Conclusions: AMH may reflect a unique biomarker of NASH in premenopausal women and findings suggest a novel link between reproductive aging and histologic severity of NAFLD in women.
AB - Background & Aims: Antimüllerian hormone (AMH) is a marker of ovarian reserve with emerging data linking lower levels to some metabolic and inflammatory diseases in women. Whether AMH levels influence nonalcoholic fatty liver disease (NAFLD) is unknown. Methods: Leveraging the NASH Clinical Research Network we determined the association of AMH levels within 6 months of liver biopsy with presence and severity of histologic measures of NAFLD in premenopausal women. Outcomes included presence of nonalcoholic steatohepatitis (NASH), presence and severity of fibrosis, and NAFLD Activity Score and its components. Logistic and ordinal logistic regression models were adjusted for age, race/ethnicity, homeostatic model assessment for insulin resistance, body mass index, dyslipidemia, polycystic ovary syndrome, estrogen-progestin use, and menstrual cyclicity. Results: Median cohort age was 35 years; 73% were white and 24% Hispanic. Thirty-three percent had diabetes, 81% had obesity, and 95% had dyslipidemia. On biopsy 71% had NASH, 68% had any fibrosis, and 15% had advanced fibrosis. On adjusted analysis (n = 205), higher AMH quartiles were inversely associated with NAFLD histology including prevalent NASH (adjusted odds ratio [AOR], 0.64; 95% confidence interval [CI], 0.41–1.00), NAFLD Activity Score ≥5 (AOR, 0.52; 95% CI, 0.35–0.77), Mallory hyaline (AOR, 0.54; 95% CI, 0.35–0.82), and higher fibrosis stage (AOR, 0.70; 95% CI, 0.51–0.98). The protective effects of AMH were more pronounced among women without polycystic ovary syndrome (n = 164), including lower odds of NASH (AOR, 0.53; 95% CI, 0.32–0.90) and any NASH fibrosis (AOR, 0.54; 95% CI, 0.32–0.93). Conclusions: AMH may reflect a unique biomarker of NASH in premenopausal women and findings suggest a novel link between reproductive aging and histologic severity of NAFLD in women.
KW - Hepatic Fibrosis
KW - Nonalcoholic Fatty Liver Disease
KW - Polycystic Ovary Syndrome
KW - Reproductive Aging
KW - Sex Hormones
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U2 - 10.1016/j.cgh.2023.08.020
DO - 10.1016/j.cgh.2023.08.020
M3 - Article
C2 - 37678489
AN - SCOPUS:85173222510
SN - 1542-3565
VL - 22
SP - 339-346.e5
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 2
ER -