Effect of Adjunctive Estradiol on Schizophrenia Among Women of Childbearing Age: A Randomized Clinical Trial.


Journal

JAMA psychiatry
ISSN: 2168-6238
Titre abrégé: JAMA Psychiatry
Pays: United States
ID NLM: 101589550

Informations de publication

Date de publication:
01 10 2019
Historique:
pubmed: 1 8 2019
medline: 22 1 2021
entrez: 1 8 2019
Statut: ppublish

Résumé

Several lines of evidence suggest that estradiol influences the course of schizophrenia, and a previous randomized controlled trial demonstrated that transdermal estradiol improved symptoms in female patients of childbearing age. However, many initial positive findings in schizophrenia research are not later replicated. To independently replicate the results of the effect of estradiol on schizophrenia in women of childbearing age. An 8-week randomized, placebo-controlled trial performed in the Republic of Moldova between December 4, 2015, and July 29, 2016, among 200 premenopausal women aged 19 to 46 years with schizophrenia or schizoaffective disorder as defined by the DSM-5. Patients were randomized to receive a 200-μg estradiol patch or placebo patch changed twice a week added to their antipsychotic treatment. The primary outcome was the positive subscale of the Positive and Negative Syndrome Scale (PANSS; lower scores indicated fewer symptoms and higher scores indicated more symptoms), analyzed with mixed models for repeated measures on an intention-to-treat basis. A total of 100 women (median age, 38 years; interquartile range, 34-42 years) were randomized to receive an estradiol patch and 100 women (median age, 38 years; interquartile range, 31-41 years) were randomized to receive a placebo patch; the median age at baseline for the entire group of 200 women was 38.0 years (range, 19.5-46.0 years). At baseline, the mean positive PANSS score was 19.6 for both groups combined; at week 8, the mean positive PANSS score was 14.4 in the placebo group and 13.4 in the estradiol group. Compared with placebo, participants receiving add-on estradiol patches had statistically significant improvements in the primary outcome measure, PANSS positive subscale points (-0.94; 95% CI, -1.64 to -0.24; P = .008; effect size = 0.38). Post hoc heterogeneity analyses found that this effect occurred almost entirely in 100 participants older than 38.0 years (46 in placebo group vs 54 in estradiol group; difference, -1.98 points on the PANSS positive subscale; 95% CI, -2.94 to -1.02; P < .001). Younger participants did not benefit from estradiol (difference, 0.08 points on the PANSS positive subscale; 95% CI, -0.91 to 1.07; P = .87). Breast tenderness was more common in the estradiol group (n = 15) than in the placebo group (n = 1) as was weight gain (14 in estradiol group vs 1 in placebo group). The results independently replicate the finding that transdermal estradiol is an effective add-on treatment for women of childbearing age with schizophrenia and extend it, finding improvements in negative symptoms and finding that the effect could be specific to those older than 38 years. The results should be viewed in the context of the differences in the natural course of schizophrenia between females and males. ClinicalTrials.gov identifier: NCT03848234.

Identifiants

pubmed: 31365044
pii: 2738766
doi: 10.1001/jamapsychiatry.2019.1842
pmc: PMC6669788
doi:

Substances chimiques

Antipsychotic Agents 0
Estrogens 0
Estradiol 4TI98Z838E

Banques de données

ClinicalTrials.gov
['NCT03848234']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1009-1017

Commentaires et corrections

Type : CommentIn

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Auteurs

Mark Weiser (M)

Stanley Medical Research Institute, Kensington, Maryland.
Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel.
Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Linda Levi (L)

Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel.

Daisy Zamora (D)

Department of Psychiatry, University of North Carolina, Chapel Hill.
Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health, Baltimore, Maryland.

Anat Biegon (A)

Department of Radiology, Stony Brook University Medical School, Stony Brook, New York.
Department of Neurology, Stony Brook University Medical School, Stony Brook, New York.

John Paul SanGiovanni (JP)

Section on Nutritional Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland.
Department of Biochemistry and Molecular & Cellular Biology, Georgetown School of Medicine, Washington, DC.

Michael Davidson (M)

Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel.
University of Nicosia Medical School, Engomi, Cyprus.

Shimon Burshtein (S)

Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel.

Ilan Gonen (I)

Tangent Alzheimer Care, Breaza, Romania.

Paull Radu (P)

Tangent Alzheimer Care, Breaza, Romania.

Kristina Slobozean Pavalache (K)

Republican Psychiatric Hospital, Chișinău, Moldova.

Igor Nastas (I)

Psychiatry, Narcology, and Medical Psychology, State University of Medicine and Pharmaceuticals, "Nicolae Testemianu," Chisinau, Moldova.

Rina Hemi (R)

Institute of Endocrinology, Sheba Medical Center, Tel Hashomer, Israel.

Timothy Ryan (T)

Department of Psychiatry, University of Illinois, Chicago.

John M Davis (JM)

Department of Psychiatry, University of Illinois, Chicago.
Department of Psychiatry, Johns Hopkins University, Baltimore, Maryland.

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Classifications MeSH