Malmqvist Anna, Eren Feride, Schwieler Lilly, Orhan Funda, Fatouros-Bergman Helena, Flyckt Lena, Piehl Fredrik, Cervenka Simon, Bäck Magnus, Sellgren Carl M, Engberg Göran, Erhardt Sophie
Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet & Stockholm Health Care Services, Region Stockholm, Sweden.
Schizophrenia (Heidelb). 2025 Jun 14;11(1):88. doi: 10.1038/s41537-025-00633-x.
Patients with schizophrenia have a threefold higher mortality from cardiovascular disease than people in the general population. Atherosclerosis is linked to immune activation, a process tentatively entwined with the underlying pathophysiological mechanisms of schizophrenia. The aim of the present study was to investigate an extensive array of cardiovascular biomarkers in individuals experiencing their first episode of psychosis (FEP), either drug-naïve or exposed to short-term antipsychotic treatment, alongside a group of healthy controls (HC). Using the OLINK Proximity Extension Assay, Cardiovascular II Panel, we analyzed plasma from 72 FEP patients, including 42 later diagnosed with schizophrenia and 54 HCs. Biomarker levels, that significantly differed between patients and controls, were correlated with symptom severity, cognitive performance and cardiovascular risk factors. Fifteen out of 92 cardiovascular biomarkers were higher in individuals with FEP compared to HC, and one biomarker was lower in FEP patients compared to HC. BMI, waist size, blood pressure, fp-glucose, HbA1c and serum lipid levels were similar between the groups. No correlations that held for multiple comparisons were seen between biomarker concentrations and symptom severity, cognitive performance or cardiovascular risk factors in FEP patients. Higher concentrations of several cardiovascular biomarkers were observed in individuals with FEP compared to in HC. This suggests that patients with FEP are at an increased risk of developing cardiovascular disease from the onset of psychosis, even before changes in traditional biomarkers are detectable. It underscores the need for innovative approaches to detect and monitor this risk early.
精神分裂症患者患心血管疾病的死亡率比普通人群高三倍。动脉粥样硬化与免疫激活有关,这一过程与精神分裂症的潜在病理生理机制存在一定关联。本研究的目的是调查首次发作精神病(FEP)的个体(无论是未服用药物还是接受短期抗精神病药物治疗)以及一组健康对照者(HC)体内广泛的心血管生物标志物。我们使用欧林克(OLINK)邻近延伸分析心血管II检测板,分析了72例FEP患者(包括42例后来被诊断为精神分裂症的患者)和54例健康对照者的血浆。患者与对照者之间存在显著差异的生物标志物水平与症状严重程度、认知表现和心血管危险因素相关。与健康对照者相比,92种心血管生物标志物中有15种在FEP个体中更高,而有一种生物标志物在FEP患者中更低。两组之间的体重指数、腰围、血压、空腹血糖、糖化血红蛋白和血脂水平相似。在FEP患者中,生物标志物浓度与症状严重程度、认知表现或心血管危险因素之间未发现经多重比较仍成立的相关性。与健康对照者相比,FEP个体中观察到几种心血管生物标志物的浓度更高。这表明FEP患者从精神病发作开始就有患心血管疾病的风险增加,甚至在传统生物标志物发生变化之前就可检测到。这凸显了早期检测和监测这种风险的创新方法的必要性。