PMID- 29896133 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 1664-0640 (Print) IS - 1664-0640 (Electronic) IS - 1664-0640 (Linking) VI - 9 DP - 2018 TI - The Impact of Aging, Psychotic Symptoms, Medication, and Brain-Derived Neurotrophic Factor on Cognitive Impairment in Japanese Chronic Schizophrenia Patients. PG - 232 LID - 10.3389/fpsyt.2018.00232 [doi] LID - 232 AB - Background: Cognitive impairment in schizophrenia can result in considerable difficulty in performing functions of daily life or social rehabilitation. Cognitive impairment in schizophrenia is related to various factors, such as the psychotic severity, aging, medication, and brain-derived neurotrophic factor (BDNF). To date, however, no studies investigating the impact of these factors on cognitive functioning in chronic schizophrenia patients have been performed. Objective: The aim of this study is to identify those factors that influence the cognitive functioning in patients with chronic schizophrenia. Methods: Sixty-five of 116 long-term hospitalized chronic schizophrenia patients (63.8 +/- 12.1 years old, M/F = 29/36) were enrolled this cross-sectional study. We investigated the relationship among the patients' age, psychotic severity, treatment medication, serum BDNF levels, and cognitive functioning (measured by the Japanese-language version of the Brief Assessment of Cognition in Schizophrenia; BACS-J). Additionally, we performed a multivariable linear regression analysis. Results: According to the partial correlation analysis, certain parameters [i.e., age, chlorpromazine (CP) equivalent, biperiden (BP) equivalent, and serum BDNF] were significantly correlated with cognitive functioning, including working memory (WM), motor function (MF), attention and processing speed (AP), and executive function (EF). For the multivariate analysis, the MF component, which had the highest correlation, was selected as the dependent variable, and the independent variables included age, Manchester Scale for chronic psychosis (ManS) total score, CP equivalent, BP equivalent, serum BDNF, estimated full scale IQ, and years of education. According to the multiple regression analysis of this model, R (multiple regression coefficient) was 0.542, the adjusted R(2) (coefficient of determination) was 0.201, and only BP equivalent (beta = -0.305, p = 0.030), but not age, ManS score, CP equivalent, or serum BDNF, could significantly explain MF at the 5% significant level. Conclusion: In conclusion, aging, medication (administering more antipsychotics or anticholinergics), and serum BDNF concentration are significantly correlated with cognitive dysfunction in chronic schizophrenia patients but not with the severity of psychotic symptoms. Furthermore, only the anticholinergic dosage had a significant causal relationship with MF. Thus, the use of anticholinergics in chronic schizophrenia patients with deteriorating cognitive functioning must be reconsidered. FAU - Atake, Kiyokazu AU - Atake K AD - Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. FAU - Nakamura, Tomoyuki AU - Nakamura T AD - Department of Neuropsychiatry, Kurume University, Kurume, Japan. FAU - Ueda, Nobuhisa AU - Ueda N AD - Tsutsumi Hospital, Okagaki, Japan. FAU - Hori, Hikaru AU - Hori H AD - Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. FAU - Katsuki, Asuka AU - Katsuki A AD - Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. FAU - Yoshimura, Reiji AU - Yoshimura R AD - Department of Psychiatry, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. LA - eng PT - Journal Article DEP - 20180529 PL - Switzerland TA - Front Psychiatry JT - Frontiers in psychiatry JID - 101545006 PMC - PMC5987164 OTO - NOTNLM OT - Japanese-language version of the Brief Assessment of Cognition in Schizophrenia OT - aging OT - brain-derived neurotrophic factor OT - cognitive impairment OT - schizophrenia EDAT- 2018/06/14 06:00 MHDA- 2018/06/14 06:01 PMCR- 2018/05/29 CRDT- 2018/06/14 06:00 PHST- 2017/12/29 00:00 [received] PHST- 2018/05/11 00:00 [accepted] PHST- 2018/06/14 06:00 [entrez] PHST- 2018/06/14 06:00 [pubmed] PHST- 2018/06/14 06:01 [medline] PHST- 2018/05/29 00:00 [pmc-release] AID - 10.3389/fpsyt.2018.00232 [doi] PST - epublish SO - Front Psychiatry. 2018 May 29;9:232. doi: 10.3389/fpsyt.2018.00232. eCollection 2018.