Treatment Resistance in Schizophrenia Is Associated with Attention Deficit/Hyperactivity Disorder and Gut Microbiota: A Genetic Correlation and Mendelian Randomization Study.

IF 2.3 4区 心理学 Q3 NEUROSCIENCES Neuropsychobiology Pub Date : 2023-01-01 DOI:10.1159/000528316
Bolun Cheng, Shiqiang Cheng, Chun'e Li, Wenming Wei, Li Liu, Peilin Meng, Xuena Yang, Yumeng Jia, Yan Wen, Feng Zhang
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引用次数: 1

Abstract

Introduction: Observational studies highlight associations of common diseases with individual schizophrenia symptoms. However, it is unclear whether these diseases are associated with individual treatment-resistant schizophrenia (TRS). We aimed to explore the genetic associations between common immune diseases, metabolic diseases, psychiatric disorders, gut microbiota and TRS.

Methods: Genome-wide association study (GWAS) summary data of European participants (n = ∼456,327) included TRS, 11 psychiatric disorders, 23 immune and metabolic diseases, body mass index, height, and 211 gut microbiota. In this genetic correlation and two-sample Mendelian randomization (MR) study, linkage disequilibrium score (LDSC) regression was applied to infer genetic correlation estimates. Two-sample MR tested potential causal associations of genetic variants associated with common immune diseases, metabolic diseases, psychiatric disorders, and gut microbiota with TRS.

Results: LDSC revealed candidate associations between attention deficit/hyperactivity disorder (ADHD), schizophrenia, intestinal infectious diseases, obesity and TRS (genetic correlation range, 0.230-0.702; p < 0.05). Two-sample MR analyses suggested that ADHD was positively associated with TRS (estimate [SE] = 0.204 [0.073], p = 0.005), a finding that remained stable across statistical models. Besides, schizophrenia and genus Barnesiella levels were causally associated with TRS but not consistent across MR approaches.

Conclusion: This study reports genetic correlations between ADHD, schizophrenia, intestinal infectious diseases, obesity and TRS. The study also found that genus Barnesiella was associated with TRS. These findings may have clinical implications, highlighting the possible strategy for TRS prevention.

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精神分裂症治疗抵抗与注意缺陷/多动障碍和肠道微生物群相关:遗传相关性和孟德尔随机化研究
观察性研究强调了常见疾病与个体精神分裂症症状的关联。然而,尚不清楚这些疾病是否与个体治疗抵抗性精神分裂症(TRS)相关。我们旨在探索常见免疫疾病、代谢性疾病、精神疾病、肠道微生物群与TRS之间的遗传关联。方法:欧洲参与者的全基因组关联研究(GWAS)汇总数据(n = ~ 456,327)包括TRS、11种精神疾病、23种免疫和代谢疾病、体重指数、身高和211种肠道微生物群。在这个遗传相关和双样本孟德尔随机化(MR)研究中,连锁不平衡评分(LDSC)回归应用于推断遗传相关估计。双样本磁共振检测了与常见免疫疾病、代谢性疾病、精神疾病和肠道微生物群相关的遗传变异与TRS的潜在因果关系。结果:LDSC显示注意缺陷/多动障碍(ADHD)、精神分裂症、肠道传染病、肥胖与TRS存在候选相关性(遗传相关范围为0.230 ~ 0.702;P < 0.05)。双样本MR分析表明ADHD与TRS呈正相关(估计[SE] = 0.204 [0.073], p = 0.005),这一发现在各统计模型中保持稳定。此外,精神分裂症和巴尼斯氏菌属水平与TRS有因果关系,但在不同的MR方法中并不一致。结论:本研究报告了ADHD、精神分裂症、肠道传染病、肥胖和TRS之间的遗传相关性。该研究还发现巴尼斯氏菌属与TRS有关。这些发现可能具有临床意义,强调了TRS预防的可能策略。
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来源期刊
Neuropsychobiology
Neuropsychobiology 医学-精神病学
CiteScore
7.20
自引率
0.00%
发文量
26
审稿时长
6 months
期刊介绍: The biological approach to mental disorders continues to yield innovative findings of clinical importance, particularly if methodologies are combined. This journal collects high quality empirical studies from various experimental and clinical approaches in the fields of Biological Psychiatry, Biological Psychology and Neuropsychology. It features original, clinical and basic research in the fields of neurophysiology and functional imaging, neuropharmacology and neurochemistry, neuroendocrinology and neuroimmunology, genetics and their relationships with normal psychology and psychopathology. In addition, the reader will find studies on animal models of mental disorders and therapeutic interventions, and pharmacoelectroencephalographic studies. Regular reviews report new methodologic approaches, and selected case reports provide hints for future research. ''Neuropsychobiology'' is a complete record of strategies and methodologies employed to study the biological basis of mental functions including their interactions with psychological and social factors.
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