OBJECTIVES: To examine whether a number of nutritional and familial factors were associated with menopausal development. METHODS: A prospective postal survey amongst a random sample of 1227 women aged 47 to 51 who were premenopausal in a cross-sectional survey 2 years previously. Women were classed into three groups; premenopause (regular menstruation); irregular menstruation; postmenopausal (absence of menstrual cycle for at least 6 months). Proportional odds regression was used to identify those factors which were independently predictive of subsequent menopausal development. RESULTS: There was an 80% (n = 983) survey response rate. After exclusion of current HRT users (n = 178); 150 (19%) women were postmenopausal, 277 (34%) had erratic menstruation and 378 (47%) were premenopause. There were significant univariate associations between menopausal status and age (P < 0.001), age of maternal menopause (P = 0.006), alcohol consumption (P = 0.005) and social class (P = 0.03). Maternal age and alcohol consumption were significantly correlated with estradiol levels (r = 0.45, P = 0.02, and r = 0.61, P = 0.02 for maternal age and alcohol consumption, respectively). In proportional odds regression analyses, age, maternal menopausal age, alcohol consumption and smoking were independently associated with menopausal status. CONCLUSIONS: These results suggest that, (1) there is a strong familial association in menopausal age, and (2) moderate consumption of alcohol is associated with delayed menopausal development.
OBJECTIVES: To examine whether a number of nutritional and familial factors were associated with menopausal development. METHODS: A prospective postal survey amongst a random sample of 1227 women aged 47 to 51 who were premenopausal in a cross-sectional survey 2 years previously. Women were classed into three groups; premenopause (regular menstruation); irregular menstruation; postmenopausal (absence of menstrual cycle for at least 6 months). Proportional odds regression was used to identify those factors which were independently predictive of subsequent menopausal development. RESULTS: There was an 80% (n = 983) survey response rate. After exclusion of current HRT users (n = 178); 150 (19%) women were postmenopausal, 277 (34%) had erratic menstruation and 378 (47%) were premenopause. There were significant univariate associations between menopausal status and age (P < 0.001), age of maternal menopause (P = 0.006), alcohol consumption (P = 0.005) and social class (P = 0.03). Maternal age and alcohol consumption were significantly correlated with estradiol levels (r = 0.45, P = 0.02, and r = 0.61, P = 0.02 for maternal age and alcohol consumption, respectively). In proportional odds regression analyses, age, maternal menopausal age, alcohol consumption and smoking were independently associated with menopausal status. CONCLUSIONS: These results suggest that, (1) there is a strong familial association in menopausal age, and (2) moderate consumption of alcohol is associated with delayed menopausal development.
Authors: Brian W Whitcomb; Alexandra Purdue-Smithe; Susan E Hankinson; JoAnn E Manson; Bernard A Rosner; Elizabeth R Bertone-Johnson Journal: J Clin Endocrinol Metab Date: 2018-10-01 Impact factor: 5.958
Authors: Alexandra C Purdue-Smithe; Brian W Whitcomb; Kathleen L Szegda; Maegan E Boutot; JoAnn E Manson; Susan E Hankinson; Bernard A Rosner; Lisa M Troy; Karin B Michels; Elizabeth R Bertone-Johnson Journal: Am J Clin Nutr Date: 2017-05-10 Impact factor: 7.045
Authors: D Stock; J A Knight; J Raboud; M Cotterchio; S Strohmaier; W Willett; A H Eliassen; B Rosner; S E Hankinson; E Schernhammer Journal: Hum Reprod Date: 2019-03-01 Impact factor: 6.918
Authors: Jennifer D Peck; B Mitchell Peck; Valerie J Skaggs; Miyuki Fukushima; Howard B Kaplan Journal: J Adolesc Health Date: 2010-09-16 Impact factor: 5.012
Authors: Brian W Whitcomb; Alexandra C Purdue-Smithe; Kathleen L Szegda; Maegan E Boutot; Susan E Hankinson; JoAnn E Manson; Bernard Rosner; Walter C Willett; A Heather Eliassen; Elizabeth R Bertone-Johnson Journal: Am J Epidemiol Date: 2018-04-01 Impact factor: 4.897