
Lifetime number of years of menstruation as a risk index for postmenopausal endometrial cancer in the Norwegian Women and Cancer Study
Author(s) -
Gavrilyuk Oxana,
Braaten Tonje,
Weiderpass Elisabete,
Licaj Idlir,
Lund Eiliv
Publication year - 2018
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.1111/aogs.13381
Subject(s) - medicine , endometrial cancer , hazard ratio , proportional hazards model , gynecology , attributable risk , confounding , body mass index , confidence interval , population , cancer , obstetrics , relative risk , demography , epidemiology , environmental health , sociology
Lifetime number of years of menstruation ( LNYM ) reflects a woman's cumulative exposure to endogenous estrogen and can be used as a measure of the combined effect of reproductive factors related to endometrial cancer ( EC ) risk. Material and methods We aimed to study the association between LNYM and EC risk among postmenopausal women and calculate the population attributable fraction of EC for different LNYM categories. Our study sample consisted of 117 589 women from the Norwegian Women and Cancer ( NOWAC ) Study. All women were aged 30‐70 years at enrollment and completed a baseline questionnaire between 1991 and 2006. Women were followed up for EC to December 2014 through linkages to national registries. We used Cox proportional hazards models to estimate hazard ratios with 95% confidence intervals (95% CI s), adjusted for potential confounders. Results In all, 720 women developed EC . We found a statistically significant, positive dose‐response relationship between LNYM and EC , with a 9.1% higher risk for each additional year of LNYM ( P for trend < .001). Using the LNYM category ≥40 as a reference, the hazard ratios for LNYM <25, 25‐29, 30‐34, 35‐39 were 0.17 (95% CI 0.22‐0.27), 0.25 (95% CI 0.17‐0.36), 0.43 (95% CI 0.32‐0.58), and 0.68 (95% CI 0.51‐0.92), respectively. The association between LNYM and EC was independent of incomplete pregnancies, menopausal hormone therapy, diabetes, and body mass index. When considering the population attributable fraction, 67% of EC was estimated to be attributable to LNYM ≥25 years. Conclusions Our study supports that increasing LNYM is an important and independent predictor of EC risk.