Tokarski Rudy, Barbosa Susana, Pignon Baptiste, Aouizerate Bruno, Andrieu Christelle, Andre Myrtille, Boukouaci Wahid, Capdevielle Delphine, Chereau Isabelle, Dondé Clément, Kobayashi Julie Clauss, Dorey J M, Dubertret Caroline, Fakra Eric, Fond Guillaume, Goze Tudy, Leignier Sylvain, Llorca Pierre-Michel, Mallet Jasmina, Misdrahi David, Oriol Nicolas, Rey Romain, Roux Paul, Schürhoff Franck, Schorr Benoit, Szöke Andrei, Urbach Mathieu, Very Etienne, Wu Ching-Li, Leboyer Marion, Tamouza Ryad, Godin Ophelia
Université Paris Est Créteil (UPEC), INSERM, Institut Henri Mondor the Recherche Biomédicale, Laboratoire Neuro-Psychiatrie Translationnelle, Créteil, France.
Université Côte d'Azur, Centre National de la Recherche Scientifique, Institut de Pharmacologie Moléculaire et Cellulaire, Valbonne, France.
J Psychosom Res. 2025 Aug;195:112192. doi: 10.1016/j.jpsychores.2025.112192. Epub 2025 Jun 22.
Recent studies on Metabolic dysfunction-associated fatty liver (MAFLD) in schizophrenia show inconsistent findings, often based on small or specific samples. This study aims to assess the prevalence of MAFLD and its sociodemographic, clinical, and treatment-related risk factors in a large cohort of chronic patients with schizophrenia. A secondary goal is to identify an immuno-inflammatory signature associated with MAFLD.
1009 stable outpatients with schizophrenia were included in the cross-sectional analysis. Individuals with liver disease, hepatitis B/C, or current alcohol use disorder were excluded. MAFLD was screened using the Fatty Liver Index (FLI), with FLI > 60 indicating MAFLD. Risk factors were assessed using multivariate logistic regression, and inflammatory markers were analysed with penalized logistic regression.
In a sample of 1009 individuals with schizophrenia, MAFLD prevalence was 36.6 %, higher in men than in women (38.3 % vs 32.0 %, p < 0.0001). Multivariate analysis identified male gender, older age, current smokers, mood stabilizers, antidepressant, clozapine, olanzapine and quetiapine as risk factors for MAFLD. The use of risperidone was associated with a lower risk of MAFLD (0.63 (0.42-0.94). Elevated levels of inflammatory markers such as TNF-α, CRP, and IL-12/IL-23p40 were also linked to a higher likelihood of MAFLD.
Although not generalizable to all patients with schizophrenia, this study confirms the high prevalence of MAFLD in individuals with schizophrenia. Psychiatrists should promote healthy lifestyle changes, such as weight control, improved diet, better sleep, and increased physical activity, to improve both physical health and quality of life in these patients.
近期关于精神分裂症患者代谢功能障碍相关脂肪性肝病(MAFLD)的研究结果不一致,且往往基于小样本或特定样本。本研究旨在评估一大群慢性精神分裂症患者中MAFLD的患病率及其社会人口学、临床和治疗相关危险因素。第二个目标是识别与MAFLD相关的免疫炎症特征。
1009名病情稳定的精神分裂症门诊患者纳入横断面分析。排除患有肝病、乙型/丙型肝炎或当前存在酒精使用障碍的个体。使用脂肪肝指数(FLI)筛查MAFLD,FLI>60表明存在MAFLD。使用多因素逻辑回归评估危险因素,并使用惩罚逻辑回归分析炎症标志物。
在1009名精神分裂症患者样本中,MAFLD患病率为36.6%,男性高于女性(38.3%对32.0%,p<0.0001)。多因素分析确定男性、年龄较大、当前吸烟者、心境稳定剂、抗抑郁药、氯氮平、奥氮平和喹硫平为MAFLD的危险因素。使用利培酮与较低的MAFLD风险相关(0.63(0.42 - 0.94))。炎症标志物如肿瘤坏死因子-α、C反应蛋白和白细胞介素-12/白细胞介素-23p40水平升高也与MAFLD的较高可能性相关。
尽管本研究结果不能推广至所有精神分裂症患者,但证实了精神分裂症患者中MAFLD的高患病率。精神科医生应促进健康的生活方式改变,如控制体重、改善饮食、更好的睡眠和增加体育活动,以改善这些患者的身体健康和生活质量。