TY - JOUR
T1 - Major depression, antidepressant use, and male and female fertility
AU - Reproductive Medicine Network
AU - Evans-Hoeker, Emily A.
AU - Eisenberg, Esther
AU - Diamond, Michael P.
AU - Legro, Richard S.
AU - Alvero, Ruben
AU - Coutifaris, Christos
AU - Casson, Peter R.
AU - Christman, Gregory M.
AU - Hansen, Karl R.
AU - Zhang, Heping
AU - Santoro, Nanette
AU - Steiner, Anne Z.
AU - Bartlebaugh, C.
AU - Dodson, W.
AU - Estes, S.
AU - Gnatuk, C.
AU - Ladda, R.
AU - Ober, J.
AU - Brzyski, R.
AU - Easton, C.
AU - Hernandez, A.
AU - Leija, M.
AU - Pierce, D.
AU - Robinson, R.
AU - Ager, J.
AU - Awonuga, A.
AU - Cedo, L.
AU - Cline, A.
AU - Collins, K.
AU - Krawetz, S.
AU - Puscheck, E.
AU - Singh, M.
AU - Yoscovits, M.
AU - Lecks, K.
AU - Martino, L.
AU - Marunich, R.
AU - Comfort, A.
AU - Crow, M.
AU - Hohmann, A.
AU - Mallette, S.
AU - Smith, Y.
AU - Randolph, J.
AU - Fisseha, S.
AU - Ohl, D.
AU - Ringbloom, M.
AU - Tang, J.
AU - Bates, W.
AU - Mason, S.
AU - Craig, L. B.
AU - Zornes, C.
N1 - Funding Information:
E.A.E.-H. has nothing to disclose. E.E. has nothing to disclose. M.P.D. has nothing to disclose. R.S.L. reports personal fees from Odega, Abbvie, Kindex, Fractyl, and Bayer and grants from Ferring Phamaceuticals. R.A. has nothing to disclose. C.C. has nothing to disclose. P.R.C. has nothing to disclose. G.M.C. reports grants from and advisory board membership for Abbvie Pharmaceuticals. K.R.H. reports grants from Roche Diagnostics and Ferring International Pharmascience Center US. H.Z. has nothing to disclose. N.S. has nothing to disclose. A.Z.S. has nothing to disclose.
Funding Information:
Supported by National Institutes of Health (NIH)/Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) grants R25 HD075737 (to N.S. and E.E.H), U10 HD077680 (to K.R.H) U10HD077844 (to A.Z.S), U10 HD39005 (to M.P.D.), U10 HD38992 (to R.S.L.), U10 HD38998 (to R.A.), HD055944 (to P.R.C.), U10 HD055936 (to G.M.C.), U10HD055925 (to H.Z.), and U10 U54-HD29834 (to the University of Virginia Center for Research in Reproduction Ligand Assay and Analysis Core of the Specialized Cooperative Centers Program in Reproduction and Infertility Research), NIH grant UL1 TR000127 (to Pennsylvania State University), and the American Recovery and Reinvestment Act. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NICHD or NIH.
Funding Information:
Supported by National Institutes of Health (NIH)/Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) grants R25 HD075737 (to N.S. and E.E.H), U10 HD077680 (to K.R.H) U10HD077844 (to A.Z.S), U10 HD39005 (to M.P.D.), U10 HD38992 (to R.S.L.), U10 HD38998 (to R.A.), HD055944 (to P.R.C.), U10 HD055936 (to G.M.C.), U10HD055925 (to H.Z.), and U10 U54-HD29834 (to the University of Virginia Center for Research in Reproduction Ligand Assay and Analysis Core of the Specialized Cooperative Centers Program in Reproduction and Infertility Research), NIH grant UL1 TR000127 (to Pennsylvania State University), and the American Recovery and Reinvestment Act. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NICHD or NIH.
Publisher Copyright:
© 2018 American Society for Reproductive Medicine
PY - 2018/5
Y1 - 2018/5
N2 - Objective: To determine if maternal major depression (MD), antidepressant use, or paternal MD are associated with pregnancy outcomes after non-IVF fertility treatments. Design: Cohort study. Setting: Clinics. Patient(s): Participants in two randomized trials: PPCOS II (clomiphene citrate versus letrozole for polycystic ovary syndrome), and AMIGOS (gonadotropins versus clomiphene citrate versus letrozole for unexplained infertility). Intervention(s): Female and male partners completed the Patient Health Questionnaire (PHQ-9). Female medication use was collected. PHQ-9 score ≥10 was used to define currently active MD. Main Outcome Measure(s): Primary outcome: live birth. Secondary outcomes: pregnancy, first-trimester miscarriage. Poisson regression models were used to determine relative risks after adjusting for age, race, income, months trying to conceive, smoking, and study (PPCOS II versus AMIGOS). Result(s): Data for 1,650 women and 1,608 men were included. Among women not using an antidepressant, the presence of currently active MD was not associated with poorer fertility outcomes (live birth, miscarriage), but rather was associated with a slightly increased likelihood of pregnancy. Maternal antidepressant use (n = 90) was associated with increased risk of miscarriage, and male partners with currently active MD were less likely to achieve conception. Conclusion(s): Currently active MD in the female partner does not negatively affect non-IVF treatment outcomes; however, currently active MD in the male partner may lower the likelihood of pregnancy. Maternal antidepressant use is associated with first-trimester pregnancy loss, which may depend upon the type of antidepressant. Clinical Trial Registration Numbers: NCT00719186 and NCT01044862.
AB - Objective: To determine if maternal major depression (MD), antidepressant use, or paternal MD are associated with pregnancy outcomes after non-IVF fertility treatments. Design: Cohort study. Setting: Clinics. Patient(s): Participants in two randomized trials: PPCOS II (clomiphene citrate versus letrozole for polycystic ovary syndrome), and AMIGOS (gonadotropins versus clomiphene citrate versus letrozole for unexplained infertility). Intervention(s): Female and male partners completed the Patient Health Questionnaire (PHQ-9). Female medication use was collected. PHQ-9 score ≥10 was used to define currently active MD. Main Outcome Measure(s): Primary outcome: live birth. Secondary outcomes: pregnancy, first-trimester miscarriage. Poisson regression models were used to determine relative risks after adjusting for age, race, income, months trying to conceive, smoking, and study (PPCOS II versus AMIGOS). Result(s): Data for 1,650 women and 1,608 men were included. Among women not using an antidepressant, the presence of currently active MD was not associated with poorer fertility outcomes (live birth, miscarriage), but rather was associated with a slightly increased likelihood of pregnancy. Maternal antidepressant use (n = 90) was associated with increased risk of miscarriage, and male partners with currently active MD were less likely to achieve conception. Conclusion(s): Currently active MD in the female partner does not negatively affect non-IVF treatment outcomes; however, currently active MD in the male partner may lower the likelihood of pregnancy. Maternal antidepressant use is associated with first-trimester pregnancy loss, which may depend upon the type of antidepressant. Clinical Trial Registration Numbers: NCT00719186 and NCT01044862.
KW - Infertility
KW - antidepressant
KW - depression
UR - http://www.scopus.com/inward/record.url?scp=85047205082&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85047205082&partnerID=8YFLogxK
U2 - 10.1016/j.fertnstert.2018.01.029
DO - 10.1016/j.fertnstert.2018.01.029
M3 - Article
C2 - 29778387
AN - SCOPUS:85047205082
SN - 0015-0282
VL - 109
SP - 879
EP - 887
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 5
ER -