Antimüllerian hormone and leukocyte aging markers in the Coronary Artery Risk Development in Young Adults study.
antimüllerian hormone (AMH)
epigenetic
mitochondrial DNA copy number
telomere
Journal
Fertility and sterility
ISSN: 1556-5653
Titre abrégé: Fertil Steril
Pays: United States
ID NLM: 0372772
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
received:
12
01
2022
revised:
30
03
2022
accepted:
31
03
2022
pubmed:
25
5
2022
medline:
23
6
2022
entrez:
24
5
2022
Statut:
ppublish
Résumé
To examine whether premenopausal reproductive age, as indicated by serum antimüllerian hormone (AMH), is associated with leukocyte aging biomarkers. Prospective cohort analysis. The Coronary Artery Risk Development in Young Adults study, a population-based study of Black and White adults from four US communities (Birmingham, AL; Chicago, IL; Minneapolis, MN; Oakland, CA). Premenopausal women with serum AMH measures at examination year 15 as well as leukocyte aging markers. None. Telomere length, mitochondrial deoxyribonucleic acid (mtDNA) copy number, and intrinsic and extrinsic epigenetic age acceleration (EAA) at examination years 15, 20, and 25 as well as change between examination years. Women were 40.2 (standard deviation, 3.7) years of age at examination year 15 when the AMH and initial measures of telomere length and mtDNA copy number (n = 386) were obtained and EAA occurred. After adjustment for chronological age, race, and smoking history, AMH quartile at examination year 15 was not associated with telomere length at examination years 15 and 25 or telomere length change between these years, mtDNA copy number at examination years 15 and 25 or change between these years, or intrinsic EAA at examination years 15 and 20 or change between these years. Women in the second AMH quartile had faster extrinsic EAA than women in the lowest AMH quartile (β-coefficient, 1.84; 95% confidence interval, 0.20-3.49). In a population-based cohort, AMH did not have associations with leukocyte telomere length, mtDNA copy number, or intrinsic EAA.
Identifiants
pubmed: 35610095
pii: S0015-0282(22)00242-4
doi: 10.1016/j.fertnstert.2022.03.021
pmc: PMC10598775
mid: NIHMS1930279
pii:
doi:
Substances chimiques
Biomarkers
0
DNA, Mitochondrial
0
Anti-Mullerian Hormone
80497-65-0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
125-133Subventions
Organisme : NHLBI NIH HHS
ID : HHSN268201800004I
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL065611
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201800005I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201800006I
Pays : United States
Organisme : NHLBI NIH HHS
ID : K23 HL087114
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201800003I
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201800007I
Pays : United States
Organisme : NICHD NIH HHS
ID : R21 HD108508
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2022 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
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