Peking University Sixth Hospital, Peking University Institute of Mental Health, Beijing 100191, China; National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing 100191, China; NHC Key Laboratory of Mental Health (Peking University), Beijing 100191, China.
Peking University Sixth Hospital, Peking University Institute of Mental Health, Beijing 100191, China; National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing 100191, China; NHC Key Laboratory of Mental Health (Peking University), Beijing 100191, China; PKU-IDG/McGovern Institute for Brain Research, Peking University, Beijing 100871, China; Chinese Institute for Brain Research, Beijing 102206, China.
Psychiatry Res. 2023 Jun;324:115226. doi: 10.1016/j.psychres.2023.115226. Epub 2023 Apr 24.
Co-occurrence of antipsychotic-induced weight gain (AIWG) and therapeutic response (TR) did exist in clinic but was rarely studied. This study aims to identify potential TR/ AIWG biotypes and explore the clinical, genetic and neuroimaging features. This study enrolled 3030 patients to identify potential TR/AIWG biotypes and explore the clinical, genetic and neuroimaging features. We found three biotypes: TR+nonAIWG (46.91%), TR+AIWG (18.82%), and nonTR+nonAIWG (34.27%). TR+AIWG showed lower weight and lipid level at baseline, but higher changing rate, and higher genetic risk of obesity than TR+nonAIWG and nonTR+nonAIWG. GWAS identified ADIPOQ gene related to TR+AIWG biotypes and top-ranked loci enriched in one-carbon metabolic process, which related to both schizophrenia and metabolic dysfunction. Genetically predicted TR+AIWG was associated with higher odds of diabetes (OR=1.05). The left supplementary motor area was significantly negatively correlated with PRS of obesity. The distinguishing ability with multi-omics data to identify TR+AIWG reached 0.787. In a word, the "thin" patients with a higher risk of obesity are the target population of early intervention.
抗精神病药引起的体重增加(AIWG)与治疗反应(TR)在临床上确实同时存在,但很少有研究对此进行探讨。本研究旨在确定潜在的 TR/AIWG 生物型,并探索其临床、遗传和神经影像学特征。本研究纳入了 3030 名患者,以确定潜在的 TR/AIWG 生物型,并探索其临床、遗传和神经影像学特征。我们发现了三种生物型:TR+非 AIWG(46.91%)、TR+AIWG(18.82%)和非 TR+非 AIWG(34.27%)。TR+AIWG 组在基线时体重和血脂水平较低,但体重变化率较高,肥胖遗传风险高于 TR+非 AIWG 和非 TR+非 AIWG 组。全基因组关联分析(GWAS)确定了与 TR+AIWG 生物型相关的 ADIPOQ 基因,以及与精神分裂症和代谢功能障碍相关的一碳代谢过程中富集的最高排名基因座。遗传预测的 TR+AIWG 与糖尿病的发生风险增加相关(OR=1.05)。左侧补充运动区与肥胖的 PRS 呈显著负相关。使用多组学数据来识别 TR+AIWG 的区分能力达到 0.787。总之,“消瘦”且肥胖风险较高的患者是早期干预的目标人群。