{"title":"生物制剂对银屑病患者血脂及血象参数的影响","authors":"Kağan Cingöz, Gülsüm Gençoğlan","doi":"10.1007/s00403-025-04192-0","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of biological agents on laboratory parameters in patients with psoriasis remain incompletely characterized, with conflicting data reported. To investigate the effects of five biological agents on lipid profiles, hemogram parameters, inflammatory markers, and their correlation with disease activity in psoriasis patients. This retrospective study analyzed hemogram parameters (<i>n</i> = 153) and lipid profiles (<i>n</i> = 124) in psoriasis patients treated with adalimumab, etanercept, infliximab, ustekinumab, or secukinumab for ≥ 6 months. Parameters were evaluated at baseline, week 12, and week 24. Patients with conditions potentially affecting these parameters were excluded. Platelet counts decreased significantly in etanercept and secukinumab groups (<i>p</i> < 0.001, <i>p</i> < 0.05) and all patients (<i>p</i> < 0.001). Lymphocyte counts increased in adalimumab and etanercept groups (<i>p</i> < 0.001, <i>p</i> < 0.01) and all patients (<i>p</i> < 0.001). Neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio decreased significantly in adalimumab, etanercept, secukinumab groups (<i>p</i> < 0.05). Triglyceride levels increased in the ustekinumab group (10.91%) and all patients (3.2%) (<i>p</i> < 0.05). Total cholesterol, LDL, HDL, and atherogenic index showed no significant changes. A strong positive correlation was found between neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio changes (<i>r</i> = 0.646, <i>p</i> < 0.001). Biological agents have specific effects on hematological and lipid parameters in psoriasis patients. The observed changes in inflammatory markers and triglycerides suggest the importance of laboratory monitoring during biological therapy.</p></div>","PeriodicalId":8203,"journal":{"name":"Archives of Dermatological Research","volume":"317 1","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of biological agents on lipid profile and hemogram parameters in patients with psoriasis\",\"authors\":\"Kağan Cingöz, Gülsüm Gençoğlan\",\"doi\":\"10.1007/s00403-025-04192-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The effects of biological agents on laboratory parameters in patients with psoriasis remain incompletely characterized, with conflicting data reported. To investigate the effects of five biological agents on lipid profiles, hemogram parameters, inflammatory markers, and their correlation with disease activity in psoriasis patients. This retrospective study analyzed hemogram parameters (<i>n</i> = 153) and lipid profiles (<i>n</i> = 124) in psoriasis patients treated with adalimumab, etanercept, infliximab, ustekinumab, or secukinumab for ≥ 6 months. Parameters were evaluated at baseline, week 12, and week 24. Patients with conditions potentially affecting these parameters were excluded. Platelet counts decreased significantly in etanercept and secukinumab groups (<i>p</i> < 0.001, <i>p</i> < 0.05) and all patients (<i>p</i> < 0.001). Lymphocyte counts increased in adalimumab and etanercept groups (<i>p</i> < 0.001, <i>p</i> < 0.01) and all patients (<i>p</i> < 0.001). Neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio decreased significantly in adalimumab, etanercept, secukinumab groups (<i>p</i> < 0.05). Triglyceride levels increased in the ustekinumab group (10.91%) and all patients (3.2%) (<i>p</i> < 0.05). Total cholesterol, LDL, HDL, and atherogenic index showed no significant changes. A strong positive correlation was found between neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio changes (<i>r</i> = 0.646, <i>p</i> < 0.001). Biological agents have specific effects on hematological and lipid parameters in psoriasis patients. The observed changes in inflammatory markers and triglycerides suggest the importance of laboratory monitoring during biological therapy.</p></div>\",\"PeriodicalId\":8203,\"journal\":{\"name\":\"Archives of Dermatological Research\",\"volume\":\"317 1\",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-04-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Dermatological Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00403-025-04192-0\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Dermatological Research","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s00403-025-04192-0","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
生物制剂对银屑病患者实验室参数的影响仍不完全表征,报告的数据相互矛盾。探讨五种生物制剂对银屑病患者血脂、血象参数、炎症标志物的影响及其与疾病活动度的相关性。这项回顾性研究分析了阿达木单抗、依那西普、英夫利昔单抗、ustekinumab或secukinumab治疗≥6个月的银屑病患者的血图参数(n = 153)和脂质谱(n = 124)。在基线、第12周和第24周评估参数。排除了可能影响这些参数的患者。依那西普组和secukinumab组的血小板计数显著下降(p < 0.001, p < 0.05),所有患者的血小板计数均显著下降(p < 0.001)。阿达木单抗组和依那西普组的淋巴细胞计数增加(p < 0.001, p < 0.01),所有患者的淋巴细胞计数增加(p < 0.001)。阿达木单抗、依那西普、secukinumab组中性粒细胞与淋巴细胞比值、血小板与淋巴细胞比值显著降低(p < 0.05)。在ustekinumab组(10.91%)和所有患者(3.2%)中甘油三酯水平升高(p < 0.05)。总胆固醇、低密度脂蛋白、高密度脂蛋白及动脉粥样硬化指数无明显变化。中性粒细胞与淋巴细胞比值与血小板与淋巴细胞比值变化呈显著正相关(r = 0.646, p < 0.001)。生物制剂对银屑病患者血液学和脂质参数有特异性影响。观察到的炎症标志物和甘油三酯的变化提示在生物治疗期间实验室监测的重要性。
Effects of biological agents on lipid profile and hemogram parameters in patients with psoriasis
The effects of biological agents on laboratory parameters in patients with psoriasis remain incompletely characterized, with conflicting data reported. To investigate the effects of five biological agents on lipid profiles, hemogram parameters, inflammatory markers, and their correlation with disease activity in psoriasis patients. This retrospective study analyzed hemogram parameters (n = 153) and lipid profiles (n = 124) in psoriasis patients treated with adalimumab, etanercept, infliximab, ustekinumab, or secukinumab for ≥ 6 months. Parameters were evaluated at baseline, week 12, and week 24. Patients with conditions potentially affecting these parameters were excluded. Platelet counts decreased significantly in etanercept and secukinumab groups (p < 0.001, p < 0.05) and all patients (p < 0.001). Lymphocyte counts increased in adalimumab and etanercept groups (p < 0.001, p < 0.01) and all patients (p < 0.001). Neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio decreased significantly in adalimumab, etanercept, secukinumab groups (p < 0.05). Triglyceride levels increased in the ustekinumab group (10.91%) and all patients (3.2%) (p < 0.05). Total cholesterol, LDL, HDL, and atherogenic index showed no significant changes. A strong positive correlation was found between neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio changes (r = 0.646, p < 0.001). Biological agents have specific effects on hematological and lipid parameters in psoriasis patients. The observed changes in inflammatory markers and triglycerides suggest the importance of laboratory monitoring during biological therapy.
期刊介绍:
Archives of Dermatological Research is a highly rated international journal that publishes original contributions in the field of experimental dermatology, including papers on biochemistry, morphology and immunology of the skin. The journal is among the few not related to dermatological associations or belonging to respective societies which guarantees complete independence. This English-language journal also offers a platform for review articles in areas of interest for dermatologists and for publication of innovative clinical trials.