TY - JOUR
T1 - Later age of natural menopause among women with the pathogenic
CHEK2 c.1100delC variant
T2 - a validation study.
AU - Schreurs, Maartje A C
AU - Hollestelle, Antoinette
AU - Adank, Muriel A
AU - Louwers, Yvonne
AU - van Asperen, Christi J
AU - Ausems, Margreet G E M
AU - van de Beek, Irma
AU - Collee, Margriet J
AU - Dommering, Charlotte J
AU - Gómez García, Encarna B
AU - Wevers, Marijke R
AU - Vieveen, Emma M
AU - Yigit, Refika
AU - Schmidt, Marjanka K
AU - Visser, Jenny A
AU - Hooning, Maartje J
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2026. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.
PY - 2026/4/20
Y1 - 2026/4/20
N2 - BACKGROUND: The average age of natural menopause (ANM) for European women is 50-52 years. Reproductive risk and lifestyle factors have been found to be associated with ANM. Furthermore, a genome-wide association study found that women with a
CHEK2 variant reach ANM 3.49 years later than women without a
CHEK2 variant ('non-carriers'). With this study, we aim to validate this association within
CHEK2 c.1100delC families.
METHODS: As part of the HEreditary Breast and Ovarian cancer Netherlands (Hebon) study, all women who underwent genetic testing for pathogenic variants associated with breast or ovarian cancer were invited to participate and complete a questionnaire on established risk factors. We compared the reported ANM between groups and within selected birth cohorts. HRs and 95% CIs for the association of
CHEK2 status with ANM were estimated via Cox regression models, adjusted for age of menarche, parity, smoking status and hormonal contraceptive use.
RESULTS: We included 661
CHEK2 c.1100delC heterozygotes, 175 non-carrier relatives and 8839 unrelated non-carriers.
CHEK2 c.1100delC women reached ANM at a significantly later age (51.8±4.8 years) compared with non-carrier relatives (50.3±4.0 years) and unrelated non-carriers (49.6±4.8 years). Similar patterns were found within the birth cohorts. In Cox regression analysis, heterozygotes were associated with a later ANM compared with unrelated non-carriers (HR 1.58; 95% CI 1.21 to 2.08) and non-carrier relatives (HR 1.83; 95% CI 1.13 to 2.95).
CONCLUSION:
CHEK2 c.1100delC is associated with 1.5-2.2 years later ANM compared with non-carriers, underlining the independence of
CHEK2 c.1100delC irrespective of heritability of ANM within families.
AB - BACKGROUND: The average age of natural menopause (ANM) for European women is 50-52 years. Reproductive risk and lifestyle factors have been found to be associated with ANM. Furthermore, a genome-wide association study found that women with a
CHEK2 variant reach ANM 3.49 years later than women without a
CHEK2 variant ('non-carriers'). With this study, we aim to validate this association within
CHEK2 c.1100delC families.
METHODS: As part of the HEreditary Breast and Ovarian cancer Netherlands (Hebon) study, all women who underwent genetic testing for pathogenic variants associated with breast or ovarian cancer were invited to participate and complete a questionnaire on established risk factors. We compared the reported ANM between groups and within selected birth cohorts. HRs and 95% CIs for the association of
CHEK2 status with ANM were estimated via Cox regression models, adjusted for age of menarche, parity, smoking status and hormonal contraceptive use.
RESULTS: We included 661
CHEK2 c.1100delC heterozygotes, 175 non-carrier relatives and 8839 unrelated non-carriers.
CHEK2 c.1100delC women reached ANM at a significantly later age (51.8±4.8 years) compared with non-carrier relatives (50.3±4.0 years) and unrelated non-carriers (49.6±4.8 years). Similar patterns were found within the birth cohorts. In Cox regression analysis, heterozygotes were associated with a later ANM compared with unrelated non-carriers (HR 1.58; 95% CI 1.21 to 2.08) and non-carrier relatives (HR 1.83; 95% CI 1.13 to 2.95).
CONCLUSION:
CHEK2 c.1100delC is associated with 1.5-2.2 years later ANM compared with non-carriers, underlining the independence of
CHEK2 c.1100delC irrespective of heritability of ANM within families.
KW - Genetics, Population
UR - https://www.scopus.com/pages/publications/105030727360
U2 - 10.1136/jmg-2025-111339
DO - 10.1136/jmg-2025-111339
M3 - Article
C2 - 41690710
SN - 0022-2593
VL - 63
SP - 291
EP - 298
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
M1 - jmg-2025-111339
ER -