Interpersonal sensitivity mediates the effects of child abuse and affective temperaments on depressive symptoms in the general adult population
- PMID: 29042786
- PMCID: PMC5634385
- DOI: 10.2147/NDT.S144788
Interpersonal sensitivity mediates the effects of child abuse and affective temperaments on depressive symptoms in the general adult population
Abstract
Background: Recent studies have suggested that multiple factors interact with the onset and prognosis of major depressive disorders. In this study, we investigated how child abuse, affective temperaments, and interpersonal sensitivity are interrelated, and how they affect depressive symptoms in the general adult population.
Subjects and methods: A total of 415 volunteers from the general adult population completed the Patient Health Questionnaire-9, the Temperament Evaluation of Memphis, Pisa, Paris, and San Diego-Autoquestionnaire version, the Child Abuse and Trauma Scale, and the Interpersonal Sensitivity Measure, which are all self-administered questionnaires. Data were subjected to structural equation modeling (Mplus), and single and multiple regression analyses.
Results: The effect of child abuse on depressive symptoms was mediated by interpersonal sensitivity and 4 affective temperaments, including depressive, cyclothymic, anxious, and irritable temperaments. In addition, the effect of these temperaments on depressive symptoms was mediated by interpersonal sensitivity, indicating the indirect enhancement of depressive symptoms. In contrast to these 4 temperaments, the hyperthymic temperament did not mediate the effect of child abuse on depressive symptoms; its effect was not mediated by interpersonal sensitivity. However, a greater hyperthymic temperament predicted decreased depressive symptoms and interpersonal sensitivity, independent of any mediation effect.
Limitations: Because this is a cross-sectional study, long-term prospective studies are necessary to confirm its findings. Therefore, recall bias should be considered when interpreting the results. As the subjects were adults from the general population, the results may not be generalizable towards all patients with major depression.
Conclusion: This study suggests that child abuse and affective temperaments affect depressive symptoms partly through interpersonal sensitivity. Interpersonal sensitivity may have a major role in forming the link between abuse, affective temperament, and depression.
Keywords: TEMPS-A; affective temperament; child abuse; depression; interpersonal sensitivity; structural equation modeling.
Conflict of interest statement
Disclosure Yoshikazu Takaesu has received personal compensation from Otsuka Pharmaceutical, Meiji Seika Pharma, Eli Lilly, Eisai, Mitsubishi Tanabe Pharma, and Yoshitomiyakuhin and grants from Otsuka Pharmaceutical, Meiji Seika Pharma, and Eisai. Jiro Masuya has received personal compensation from Otsuka Pharmaceutical, Eli Lilly, Astellas, and Meiji Yasuda Mental Health Foundation and grants from Pfizer. Masahiko Ichiki has received personal compensation from Otsuka Pharmaceutical, Pfizer, Eli Lilly, Mitsubishi Tanabe Pharma, Mochida Pharmaceutical, Meiji Seika Pharma, Janssen Pharmaceutical, Takeda Pharmaceutical, MSD, Dainippon Sumitomo Pharma, and Eisai, and grants from Otsuka Pharmaceutical, Eli Lilly, Eisai, Shionogi, Takeda Pharmaceutical, MSD, and Pfizer. Additionally, Masahiko Ichiki is a member of the advisory board of Meiji Seika Pharma. Ichiro Kusumi has received personal compensation from Astellas, Chugai Pharmaceutical, Janssen Pharmaceutical, and Nippon Chemiphar, grants from AbbVie GK, Asahi Kasei Pharma, and Boehringer Ingelheim, and grants and personal compensation from Daiichi Sankyo, Dainippon Sumitomo Pharma, Eisai, Eli Lilly, GlaxoSmithKline, Kyowa Hakko Kirin, Meiji Seika Pharma, MSD, Novartis Pharma, Ono Pharmaceutical, Otsuka Pharmaceutical, Pfizer, Takeda Pharmaceutical, Mitsubishi Tanabe Pharma, Shionogi, and Yoshitomiyakuhin. Takeshi Inoue has received personal compensation from GlaxoSmithKline, Mochida Pharmaceutical, Asahi Kasei Pharma, Shionogi, Dainippon Sumitomo Pharma, and Takeda Pharmaceutical, grants from Astellas, and grants and personal compensation from Otsuka Pharmaceutical, Eli Lilly, Eisai, Mitsubishi Tanabe Pharma, Pfizer, AbbVie GK, MSD, Yoshitomiyakuhin, and Meiji Seika Pharma. Takeshi Inoue is also a member of the advisory boards of GlaxoSmithKline, Pfizer, Eli Lilly, Mochida Pharmaceutical, and Mitsubishi Tanabe Pharma. The authors report no other actual or potential conflicts of interest related this work.
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