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Association of SLC6A3 variants with treatment-resistant schizophrenia: a genetic association study of dopamine-related genes in schizophrenia.
Kogure, Masanobu; Kanahara, Nobuhisa; Miyazawa, Atsuhiro; Shiko, Yuki; Otsuka, Ikuo; Matsuyama, Koichi; Takase, Masayuki; Kimura, Makoto; Kimura, Hiroshi; Ota, Kiyomitsu; Idemoto, Keita; Tamura, Masaki; Oda, Yasunori; Yoshida, Taisuke; Okazaki, Satoshi; Yamasaki, Fumiaki; Nakata, Yusuke; Watanabe, Yoshinori; Niitsu, Tomihisa; Hishimoto, Akitoyo; Iyo, Masaomi.
Afiliação
  • Kogure M; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Kanahara N; Division of Medical Treatment and Rehabilitation, Center for Forensic Mental Health, Chiba University, Chiba, Japan.
  • Miyazawa A; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Shiko Y; Doujin-kai Kisarazu Hospital, Kisarazu, Japan.
  • Otsuka I; Biostatistics Section, Clinical Research Center, Chiba University Hospital, Chiba, Japan.
  • Matsuyama K; Department of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Takase M; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Kimura M; Douwa-kai Chiba Hospital, Funabashi, Japan.
  • Kimura H; Shoushin-kai Mobara Mental Hospital, Mobara, Japan.
  • Ota K; Chiba Psychiatric Medical Center, Chiba, Japan.
  • Idemoto K; Department of Psychiatry, Kameda Medical Center, Kamogawa, Japan.
  • Tamura M; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Oda Y; Gakuji-kai Kimura Hospital, Chiba, Japan.
  • Yoshida T; Department of Psychiatry, School of Medicine, International University of Health and Welfare, Narita, Japan.
  • Okazaki S; Doujin-kai Kisarazu Hospital, Kisarazu, Japan.
  • Yamasaki F; Choshi-kokoro Clinic, Choshi, Japan.
  • Nakata Y; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Watanabe Y; Doujin-kai Kisarazu Hospital, Kisarazu, Japan.
  • Niitsu T; Doujin-kai Kisarazu Hospital, Kisarazu, Japan.
  • Hishimoto A; Department of Cognitive Behavioral Psychology, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Iyo M; Department of Psychiatry, Chiba University Graduate School of Medicine, Chiba, Japan.
Front Psychiatry ; 14: 1334335, 2023.
Article em En | MEDLINE | ID: mdl-38476817
ABSTRACT

Background:

Most genetic analyses that have attempted to identify a locus or loci that can distinguish patients with treatment-resistant schizophrenia (TRS) from those who respond to treatment (non-TRS) have failed. However, evidence from multiple studies suggests that patients with schizophrenia who respond well to antipsychotic medication have a higher dopamine (DA) state in brain synaptic clefts whereas patients with TRS do not show enhanced DA synthesis/release pathways. Patients and

methods:

To examine the contribution (if any) of genetics to TRS, we conducted a genetic association analysis of DA-related genes in schizophrenia patients (TRS, n = 435; non-TRS, n = 539) and healthy controls (HC n = 489).

Results:

The distributions of the genotypes of rs3756450 and the 40-bp variable number tandem repeat on SLC6A3 differed between the TRS and non-TRS groups. Regarding rs3756450, the TRS group showed a significantly higher ratio of the A allele, whereas the non-TRS group predominantly had the G allele. The analysis of the combination of COMT and SLC6A3 yielded a significantly higher ratio of the putative low-DA type (i.e., high COMT activity + high SLC6A3 activity) in the TRS group compared to the two other groups. Patients with the low-DA type accounted for the minority of the non-TRS group and exhibited milder psychopathology.

Conclusion:

The overall results suggest that (i) SLC6A3 could be involved in responsiveness to antipsychotic medication and (ii) genetic variants modulating brain DA levels may be related to the classification of TRS and non-TRS.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article