Anti-Mullerian Hormone Levels are Lower in BRCA2 Mutation Carriers

Autor: A. Schanne, Mary D. Sammel, Susan M. Domchek, Clarisa R. Gracia, Maureen Prewitt, Lauren N.C. Johnson
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Anti-Mullerian Hormone
endocrine system diseases
Uterus
Comorbidity
Reference Values
skin and connective tissue diseases
Prospective cohort study
media_common
Ovarian Neoplasms
education.field_of_study
Obstetrics
Incidence
Confounding
Obstetrics and Gynecology
Middle Aged
female genital diseases and pregnancy complications
Dried blood spot
medicine.anatomical_structure
Female
Infertility
Female

Adult
Genetic Markers
endocrine system
medicine.medical_specialty
Heterozygote
Adolescent
media_common.quotation_subject
Population
Down-Regulation
Fertility
Breast Neoplasms
Polymorphism
Single Nucleotide

Article
03 medical and health sciences
Young Adult
medicine
Biomarkers
Tumor

Humans
Ovarian reserve
education
Gynecology
BRCA2 Protein
business.industry
Pennsylvania
medicine.disease
030104 developmental biology
Reproductive Medicine
Mutation
business
Ovarian cancer
Popis: To compare antimüllerian hormone (AMH) levels in women at high risk for hereditary breast and ovarian cancer compared with healthy low-risk control women.Prospective cohort.Not applicable.Reproductive-age women with a uterus and both ovaries were analyzed in four groups: BRCA1 mutation carriers, BRCA2 carriers, BRCA-negative women, and low-risk controls.Self-collected dried blood spot.AMH levels.One hundred ninety-five women were included: 55 BRCA1 carriers, 50 BRCA2 carriers, 26 BRCA negative women, and 64 low-risk controls. After adjusting for confounders, BRCA2 carriers had AMH levels that were 33% lower than control women and an increased odds of having AMH1 ng/mL. BRCA1 carriers and BRCA-negative women had AMH levels similar to control women. When analysis was restricted to regularly menstruating women younger than 40 years of age, BRCA2 carriers continued to demonstrate significantly lower AMH levels and increased likelihood of low AMH. Also, in this restricted group, BRCA-negative women demonstrated AMH levels that were 42% lower than control women. No difference in AMH was observed for BRCA1 carriers.We observed significantly lower AMH levels among BRCA2 carriers compared with low-risk control women. These results were stable across all models. BRCA-negative women also had lower AMH values, but only in models restricted to young regularly menstruating women. In contrast to earlier analyses, BRCA1 carriers had AMH values that were similar to low-risk control women, but this may be due to differences in the population studied.
Databáze: OpenAIRE