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Cited 3 time in webofscience Cited 3 time in scopus
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Depressive Symptoms in Stroke Patients: Are There Sex Differences?

Authors
Lee, Eun-JaeKim, Jong S.Chang, Dae-IlPark, Jong-HoAhn, Seong HwanCha, Jae-KwanHeo, Ji HoeSohn, Sung-IlLee, Byung-ChulKim, Dong-EogKim, Hahn YoungKim, SeongheonKwon, Do-YoungKim, JeiSeo, Woo-KeunLee, JunPark, Sang-WonKoh, Seong-HoKim, Jin YoungChoi-Kwon, Smi
Issue Date
Mar-2020
Publisher
S. Karger AG
Keywords
Stroke; Depression; Sex
Citation
Cerebrovascular Diseases, v.49, no.1, pp 19 - 25
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Cerebrovascular Diseases
Volume
49
Number
1
Start Page
19
End Page
25
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/971
DOI
10.1159/000506116
ISSN
1015-9770
1421-9786
Abstract
Background: We aimed to examine sex differences in symptom characteristics and pharmacological responses in post-stroke depressive (PSD) symptoms. Methods: This is a post hoc analysis of EMOTION (ClinicalTrials.gov, NCT01278498), a randomized, placebo-controlled, double-blind trial that examined the efficacy of escitalopram for 3 months on depression in patients with acute stroke. Depressive symptoms were evaluated using the 10-item Montgomery-angstrom sberg Depression Rating Scale (MADRS). Baseline characteristics, clinical variables, and treatment responses to escitalopram were compared between male and female patients. Treatment responses were defined as changes in MADRS (total score and its components) between baseline and 3 months and were compared between the escitalopram and placebo groups within each sex group. The least square mean was calculated to determine the independent effect of escitalopram, of which interaction was evaluated with patient sex. Results: Of the 478 patients (intention-to-treat population), 187 (39%) were female. Female patients were significantly older than male patients and demonstrated more severe depressive symptoms at baseline (male vs. female, MADRS score, mean [SD]: 9.7 +/- 8.0 vs. 12.2 +/- 8.4, p = 0.001), especially in apparent sadness, reported sadness, and reduced appetite items. These differences were significant after adjustment for age and the severity of neurologic deficits. The female escitalopram group showed a significant 3-month improvement in MADRS scores (placebo [n = 86] vs. escitalopram [n = 101], least square mean [95% CI] -2.7 [-4.1 to -1.2] vs. -5.0 [-6.4 to -3.6], p = 0.007), and this efficacy was prominent in apparent sadness, reported sadness, and pessimistic thoughts items. However, there was no significant effect of escitalopram on depressive symptoms in the male group. The treatment responses of escitalopram tended to be more pronounced in the female group, particularly in alleviating a subset of depressive symptoms such as apparent sadness (p for interaction = 0.009). Conclusion: PSD may differ according to sex in its symptom characteristics and treatment responses to escitalopram, and tailored treatment strategies for PSD may therefore be needed.
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Ansan Hospital (Department of Neurology, Ansan Hospital)
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