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揭示代谢负担:慢性斑块状银屑病的临床病理研究及其与代谢综合征的关联

Unveiling the Metabolic Burden: A Clinicopathological Study of Chronic Plaque Psoriasis and Its Association With Metabolic Syndrome.

作者信息

Shah Siddharth, Parikh Kunjal, Shah Monal L, Kothari Atul

机构信息

Department of Pathology, Sumandeep Vidyapeeth University, Vadodara, IND.

Department of Pathology, Thadiq General Hospital, Thadiq, SAU.

出版信息

Cureus. 2025 Aug 3;17(8):e89289. doi: 10.7759/cureus.89289. eCollection 2025 Aug.

DOI:10.7759/cureus.89289
PMID:40909067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12406071/
Abstract

Introduction Psoriasis is a chronic, immune-mediated inflammatory skin disease with systemic manifestations. Among its significant comorbidities, metabolic syndrome (MS) - a constellation of obesity, hypertension, dyslipidemia, and insulin resistance - has gained recognition due to its association with increased cardiovascular risk and reduced life expectancy. Chronic systemic inflammation, shared immunological pathways, and elevated pro-inflammatory cytokines are thought to underlie this association. This study aimed to explore the relationship between histopathologically confirmed chronic plaque psoriasis and MS. Methods A single-center, cross-sectional, hospital-based observational study was conducted between January 2022 and June 2023 at Smt. B. K. Shah Medical Institute and Research Centre, Gujarat. A total of 43 patients with histopathologically confirmed chronic plaque psoriasis were enrolled. Skin biopsies were stained with hematoxylin-eosin and analyzed microscopically. Metabolic parameters, including lipid profile, fasting blood glucose, and HbA1c, were measured using automated analyzers. MS was diagnosed based on National Cholesterol Education Program Adult Treatment Panel III criteria. Patients were categorized into two groups: MS (n=6, 14%) and non-MS (n=37, 86%). Clinical severity was assessed using the Psoriasis Area and Severity Index (PASI) and Body Surface Area (BSA) scoring systems. Statistical analysis was performed using IBM SPSS Statistics (IBM Corp., Armonk, USA), with significance set at p<0.05. Results Six out of 43 patients had MS (14%), with a mean age of 47.83 ± 21.78 years and male predominance of 83.3%. MS was more prevalent among married (6/6, 100%), middle-class (4/6, 66.7%), and non-vegetarian (5/6, 83.3%) male patients. PASI scores were higher (5-6) in 4/6 (66.7%) patients within the MS group, though this difference was not statistically significant. However, moderate BSA involvement (3-10%) was significantly more common among MS patients than non-MS patients. Specifically, 4/6 MS patients (66.7%) had moderate BSA involvement, whereas the majority of non-MS patients had mild involvement (<3%). This difference was found to be statistically significant (p=0.036). Compared to non-MS patients, those with MS had significantly higher weight, BMI, waist circumference, and systolic and diastolic blood pressure (all p<0.05). Biochemically, MS patients exhibited significantly elevated levels of random blood glucose, total cholesterol, triglycerides, very low-density lipoprotein, and low-density lipoprotein, alongside lower high-density lipoprotein levels (all p<0.05). Conclusion The study highlights a significant association between chronic plaque psoriasis and MS, reinforcing the need for early screening and integrated management of metabolic risk factors in psoriatic patients. A significant proportion of patients with chronic plaque psoriasis exhibit features of MS, even in the absence of clinically severe disease. These findings reinforce the need for routine MS screening in all psoriatic patients, regardless of severity scores (PASI or BSA). Dermatologists, often the first point of contact for these patients, can play a vital role in the early identification and management of metabolic risk factors through lifestyle modification and multidisciplinary care. Larger, multi-centric studies with control groups are recommended to confirm these associations and explore the pathophysiological mechanisms further.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3d4/12406071/cd192e61774e/cureus-0017-00000089289-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3d4/12406071/cd192e61774e/cureus-0017-00000089289-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3d4/12406071/cd192e61774e/cureus-0017-00000089289-i01.jpg
摘要

引言

银屑病是一种具有全身表现的慢性、免疫介导的炎症性皮肤病。在其重要的合并症中,代谢综合征(MS)——肥胖、高血压、血脂异常和胰岛素抵抗的组合——因其与心血管风险增加和预期寿命缩短有关而受到关注。慢性全身炎症、共同的免疫途径以及促炎细胞因子升高被认为是这种关联的基础。本研究旨在探讨组织病理学确诊的慢性斑块状银屑病与MS之间的关系。

方法

2022年1月至2023年6月在古吉拉特邦的Smt. B. K. Shah医学研究所和研究中心进行了一项单中心、横断面、基于医院的观察性研究。共纳入43例组织病理学确诊的慢性斑块状银屑病患者。皮肤活检标本用苏木精-伊红染色并进行显微镜分析。使用自动分析仪测量代谢参数,包括血脂谱、空腹血糖和糖化血红蛋白。根据美国国家胆固醇教育计划成人治疗小组第三次报告的标准诊断MS。患者分为两组:MS组(n = 6,14%)和非MS组(n = 37,86%)。使用银屑病面积和严重程度指数(PASI)和体表面积(BSA)评分系统评估临床严重程度。使用IBM SPSS Statistics(IBM公司,美国阿蒙克)进行统计分析,显著性设定为p<0.05。

结果

43例患者中有6例患有MS(14%),平均年龄为47.83±21.78岁,男性占比8

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