Substance use disorders in schizophrenia: Prevalence, etiology, biomarkers, and treatment

Heather Burrell Ward , Charles B. Nemeroff , Linda Carpenter , Adrienne Grzenda , William M. McDonald , Carolyn I. Rodriguez , Nina Vanessa Kraguljac
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Abstract

Substance use disorders (SUDs) are common among individuals with schizophrenia and negatively affect the clinical course of the illness. Despite the high prevalence and significant impact on outcomes, the etiology of SUDs in individuals with schizophrenia remains poorly understood. A better understanding of the etiology, shared mechanisms, temporal evolution, and complex interplay between pathophysiologies will provide the foundation for rational development of targeted therapeutics. We review the literature on the prevalence, etiology, biomarkers, and treatment for individuals with comorbid SUDs and schizophrenia. Substance use is associated with increased risk of subsequent development of schizophrenia. However, the directionality of the relationship between substance use and schizophrenia remains unclear. While several SUDs are associated with increased psychotic symptoms, others are correlated with less severe psychopathology. Individuals with schizophrenia who have more severe symptoms are more likely to have a SUD. There is evidence for shared genetic risk for SUDs and schizophrenia. Comorbid SUDs and schizophrenia share abnormalities in the mesolimbic dopamine system, affecting drug reward, sensitization, and craving. Neuroimaging studies have identified molecular, structural, and functional pathophysiology in co-occurring schizophrenia and SUDs. Neuroinflammation may also represent a shared pathophysiology between SUDs and schizophrenia. While treatments for SUDs exist, they are generally less effective and underutilized for individuals with schizophrenia. Future research is essential to understand the underlying etiology of SUDs in schizophrenia. We propose that neuromodulatory experiments can establish this etiology and identify therapeutic targets. Longitudinal studies across multiple modalities (i.e. neuroimaging, serum, genetics) may help to identify risk factors and biomarkers.

精神分裂症的物质使用障碍:患病率、病因、生物标志物和治疗
物质使用障碍(SUD)在精神分裂症患者中很常见,并对疾病的临床进程产生负面影响。尽管SUDs的发病率很高,对结果有显著影响,但对精神分裂症患者的SUDs病因仍知之甚少。更好地了解病因、共同机制、时间进化以及病理生理学之间的复杂相互作用,将为合理开发靶向治疗方法奠定基础。我们回顾了关于合并SUDs和精神分裂症患者的患病率、病因、生物标志物和治疗的文献。药物使用与随后发展为精神分裂症的风险增加有关。然而,物质使用与精神分裂症之间关系的方向性仍然不清楚。虽然一些SUD与精神病症状增加有关,但其他SUD与不太严重的精神病理学有关。症状更严重的精神分裂症患者更有可能患SUD。有证据表明SUDs和精神分裂症有共同的遗传风险。合并SUDs和精神分裂症在中边缘多巴胺系统中有共同的异常,影响药物奖励、致敏和渴望。神经影像学研究已经确定了同时发生的精神分裂症和SUDs的分子、结构和功能病理生理学。神经炎症也可能代表SUDs和精神分裂症之间的共同病理生理学。虽然存在SUD的治疗方法,但对于精神分裂症患者来说,它们通常效果较差,使用不足。未来的研究对于了解精神分裂症SUDs的潜在病因至关重要。我们提出神经调节实验可以确定这种病因并确定治疗靶点。跨多种模式(即神经成像、血清、遗传学)的纵向研究可能有助于识别风险因素和生物标志物。
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