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Neuromelanin accumulation in patients with schizophrenia: A systematic review and meta-analysis

期刊

NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
卷 132, 期 -, 页码 1205-1213

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neubiorev.2021.10.028

关键词

Dopamine; Neuromelanin; NM-MRI; Review; Schizophrenia; Substantia nigra

资金

  1. Ontario Mental Health Foundation (OMHF) Type A grant
  2. Canadian Institutes of Health Research (CIHR) [MOP-142493, MOP-141968]
  3. Japan Society for the Promotion of Science [18H02755]
  4. Japan Research Foundation for Clinical Pharmacology
  5. Takeda Science Foundation
  6. Uehara Memorial Foundation
  7. Naito Foundation
  8. Grants-in-Aid for Scientific Research [18H02755] Funding Source: KAKEN

向作者/读者索取更多资源

This study found that patients with schizophrenia have increased levels of neuromelanin in the substantia nigra, suggesting that it may serve as a potential biomarker for stratifying schizophrenia.
Although schizophrenia is associated with increased presynaptic dopamine function in the striatum, it remains unclear if neuromelanin levels, which are thought to serve as a biomarker for midbrain dopamine neuron function, are increased in patients with schizophrenia. We conducted a systematic review and meta-analysis of magnetic resonance imaging (MRI) and postmortem studies comparing neuromelanin (NM) levels between patients with schizophrenia and healthy controls (HCs). Standard mean differences were calculated to assess group differences in NM accumulation levels between patients with schizophrenia and HCs. This study included 7 articles in total. Five studies employed NM-sensitive MRI (NM-MRI) and two were postmortem brain studies. The patient group (n = 163) showed higher NM levels in the substantia nigra (SN) than HCs (n = 228) in both the analysis of the seven studies and the subgroup analysis of the 5 NM-MRI studies. This analysis suggest increased NM levels in the SN may be a potential biomarker for stratifying schizophrenia, warranting further research that accounts for the heterogeneity of this disorder.

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