TY - JOUR
T1 - Estrogen deprivation and cardiovascular disease risk in primary ovarian insufficiency
AU - Christ, Jacob P.
AU - Gunning, Marlise N.
AU - Palla, Giulia
AU - Eijkemans, Marinus J.C.
AU - Lambalk, Cornelis B.
AU - Laven, Joop S.E.
AU - Fauser, Bart C.J.M.
N1 - Funding Information:
J.P.C. reports grants from the Fulbright US Student Program, during the conduct of the study. M.N.G. reports grants from the Dutch Heart Foundation (grant no. 2013T083) and personal fees from Merck, outside the submitted work. C.B.L. reports grants from Ferring and Merck, outside the submitted work. J.S.E.L. reports grants from Ferring and Merck Serono and personal fees from Euroscreen, Danone, and Ferring during the conduct of the study. B.C.J.M.F. reports personal fees from Preglem, Ferring, Euroscreen, Ovascience, Allergan, Actavis, and the Dutch Heart Foundation, outside the submitted work. G.P. has nothing to disclose. M.J.C.E. has nothing to disclose.
Publisher Copyright:
© 2017 American Society for Reproductive Medicine
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Objective: To evaluate the association between estrogen (E) exposure and deficiency and cardiovascular disease (CVD) risk among women with primary ovarian insufficiency (POI). Design: Cross-sectional study conducted between 1996 and 2016. Setting: Tertiary referral centers. Patient(s): A total of 385 women with POI, defined by amenorrhea and FSH levels ≥40 IU/L before 40 years of age, were recruited. Intervention(s): None. Main Outcome Measure(s): Women underwent a standardized intake questionnaire including data on menstrual cyclicity. Lifetime E exposure and E-free period were assessed. Serum was analyzed for endocrine and CVD profiles. The Framingham 30-year risk of CVD was calculated. Result(s): Lifetime E exposure (mean ± SD) was 19.3 ± 7.0 years, E-free period was 3.1 ± 4.1 years, and age at screening was 34.8 ± 7.4 years. In multivariate models E-free interval associated positively with estimated risk of hard and general CVD events (β 0.18 [95% confidence interval 0.08, 0.29]; 0.20 [0.05, 0.35], respectively), and lifetime E exposure associated negatively with estimated risk of hard and general CVD events (−0.15 [−0.24, −0.05]; −0.16 [−0.29, −0.03], respectively), as well as low density lipoprotein cholesterol (−0.03 [−0.06, 0.00]) and non–high density lipoprotein cholesterol (−0.04 [−0.07, 0.00]). Conclusion(s): Prolonged E deprivation is associated with an increased estimated risk of CVD, whereas prolonged E exposure is associated with a reduced estimated risk. These results support the policy of early and continued use of E replacement therapy in women with POI. Clinical Trial Registration Number: NCT0230904.
AB - Objective: To evaluate the association between estrogen (E) exposure and deficiency and cardiovascular disease (CVD) risk among women with primary ovarian insufficiency (POI). Design: Cross-sectional study conducted between 1996 and 2016. Setting: Tertiary referral centers. Patient(s): A total of 385 women with POI, defined by amenorrhea and FSH levels ≥40 IU/L before 40 years of age, were recruited. Intervention(s): None. Main Outcome Measure(s): Women underwent a standardized intake questionnaire including data on menstrual cyclicity. Lifetime E exposure and E-free period were assessed. Serum was analyzed for endocrine and CVD profiles. The Framingham 30-year risk of CVD was calculated. Result(s): Lifetime E exposure (mean ± SD) was 19.3 ± 7.0 years, E-free period was 3.1 ± 4.1 years, and age at screening was 34.8 ± 7.4 years. In multivariate models E-free interval associated positively with estimated risk of hard and general CVD events (β 0.18 [95% confidence interval 0.08, 0.29]; 0.20 [0.05, 0.35], respectively), and lifetime E exposure associated negatively with estimated risk of hard and general CVD events (−0.15 [−0.24, −0.05]; −0.16 [−0.29, −0.03], respectively), as well as low density lipoprotein cholesterol (−0.03 [−0.06, 0.00]) and non–high density lipoprotein cholesterol (−0.04 [−0.07, 0.00]). Conclusion(s): Prolonged E deprivation is associated with an increased estimated risk of CVD, whereas prolonged E exposure is associated with a reduced estimated risk. These results support the policy of early and continued use of E replacement therapy in women with POI. Clinical Trial Registration Number: NCT0230904.
KW - Cardiovascular disease
KW - estrogen
KW - hormone replacement therapy
KW - primary ovarian insufficiency
UR - http://www.scopus.com/inward/record.url?scp=85044514021&partnerID=8YFLogxK
U2 - 10.1016/j.fertnstert.2017.11.035
DO - 10.1016/j.fertnstert.2017.11.035
M3 - Article
C2 - 29605405
AN - SCOPUS:85044514021
SN - 0015-0282
VL - 109
SP - 594-600.e1
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 4
ER -