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Observational Study
. 2025 Jul 1;25(1):631.
doi: 10.1186/s12888-025-07089-4.

Understanding anhedonia in major depressive disorder in Japan: epidemiology and unmet needs from patients' and physicians' perspectives

Affiliations
Observational Study

Understanding anhedonia in major depressive disorder in Japan: epidemiology and unmet needs from patients' and physicians' perspectives

Mami Kasahara-Kiritani et al. BMC Psychiatry. .

Abstract

Background: Anhedonia (ANH), one of the core symptoms of major depressive disorder (MDD), poses a significant health challenge. We evaluated the prevalence of ANH among MDD patients in Japan, and elucidated patient journey from patients' and physicians' perspective.

Methods: This cross-sectional observational study (April-May 2023) utilized a self-reported, online-based survey targeting the general population (non-physicians) and physicians. The general population (aged ≥ 18 years) were screened for MDD using Patient Health Questionnaire-9 (PHQ-9 ≥ 10); MDD patients were further screened for ANH using Snaith-Hamilton Pleasure Scale (SHAPS; MDD-ANH: SHAPS > 2, MDD non-ANH: SHAPS ≤ 2). The age- and gender-weighted prevalences of MDD and MDD-ANH, patient journey, and treatment goals and satisfaction between patients and physicians were reported. P-value < 0.05 was considered statistically significant.

Results: The prevalence of MDD was 3.4% (n = 514; N = 15,266) and the prevalence of ANH in MDD was 66.9% (n = 344). Mean (± standard deviation) age of MDD-ANH patients (n = 282) was 46.1 ± 12.5 years, while for MDD non-ANH patients (n = 50) was 49.6 ± 8.5 years. Physicians (n = 60) had mean 21.9 years of experience working as psychiatrists. Physicians reported that 33.9% of their MDD patients had anhedonia. MDD-ANH patients scored significantly higher (p < 0.05) than MDD non-ANH patients on all PHQ-9 items, except for feeling tired/having little energy and poor appetite/overeating. A higher percentage of MDD-ANH patients reported current prescription use for depression than MDD non-ANH patients (67.0% vs. 51.3%; p = 0.0677). Treatment duration with multiple prescriptions was significantly longer in MDD-ANH than MDD non-ANH patients (102.1 ± 89.8 vs. 53.8 ± 33.7 months; p = 0.0035). The majority of physicians (90.0%) reported that they do not focus on treating anhedonia separately from MDD. Patients with MDD-ANH perceived "reduce psychological anxiety", "control depressed mood", and "improve sleep quality" as more important treatment goals, compared to physicians' importance to avoid suicidal thoughts, restore normal social function, and regain interest in hobbies. Treatment satisfaction levels were higher among physicians than MDD-ANH patients across all treatment goals.

Conclusion: This study in Japan reported high prevalence of ANH among MDD patients which was significantly underestimated by physicians. Discordances in treatment goals and satisfaction were observed between physicians and MDD patients, highlighting the need for aligning patient and physician expectations.

Trial registration: Not applicable.

Keywords: Anhedonia; Japan; Major depressive disorder; Physicians' perspectives; Prevalence; Treatment goals; Treatment satisfaction.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: The study adhered to the ethical principles outlined in the Declaration of Helsinki and followed Good Epidemiological Practices (GEP) as defined by the International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Approval for the study protocol was obtained from the Toukeikai Kitamachi Clinic Ethical Review Board in Japan (approval number: EJP09413). Appropriate confidentiality measures were implemented throughout the study to safeguard the privacy of all respondents’ records, ensuring that individual respondents always remained unidentified. Each respondent had provided informed electronic consent prior to participating in the study. Consent for publication: Not applicable. Competing interests: MK, AW, and NL are employee of Janssen Pharmaceutical K.K., Tokyo, Japan. TK reports personal fees from Janssen Asia Pacific/Vista Health related to this work, reports grants from Sumitomo Pharma Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Eli Lilly Japan K.K., Teijin Pharma, Daiichi Sankyo Co., Ltd., EA Pharma Co., Ltd., and Eisai Co., Ltd., personal fees from Sumitomo Pharma Co., Ltd., Otsuka Pharmaceutical Co., Ltd., Takeda Pharmaceutical Co., Ltd., Eisai Co., Ltd., Meiji Seika Pharma Co., Ltd., Shionogi & Co., Ltd., Mochida Pharmaceutical Co., Janssen Pharmaceutical K.K., Janssen Asia Pacific, Vista Health, Yoshitomiyakuhin, MSD K.K., Japan Boehringer Ingelheim, Kyowa Pharmaceutical Industry Co., Ltd., Viatris, Mylan EPD, H.U. Frontier, Lundbeck Japan K.K., Nihon Medi-physics Co., Ltd., Glaxo-SmithKline, Novartis Pharma, EA Pharma Co., and Ono Pharmaceutical Co., Ltd., outside the submitted work. TW and KH are employees of Janssen Asia Pacific, a division of Johnson & Johnson Pte Ltd, Singapore. LV is an employee of Oracle Life Sciences, Singapore.

Figures

Fig. 1
Fig. 1
Study design. * MDD without diagnosis of bipolar disorder or schizophrenia. # MDD patients with self-reported diagnosis and PHQ-9 score ≥ 10; n = 93 did not complete the SHAPS questionnaire. $MDD Patients who completed all survey questions and included in analysis

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