文章摘要
亚临床甲减合并肥胖患者的血清鸢尾素NesfatiN-1水平与动脉粥样硬化的关系
Relationship between serum irisin, Nesfatin-1 levels and atherosclerosis in patients with subclinical hypothyroidism complicated with obesity
投稿时间:2025-10-15  
DOI:10.3969/j.issn.1000-0399.2026.06.009
中文关键词: 亚临床甲减  肥胖  鸢尾素  耐斯他汀-1/摄食抑制因子-1  动脉粥样硬化
英文关键词: Subclinical hypothyroidism  Obesity  Irisin  NesfatiN-1  Atherosclerosis
基金项目:吕梁市重点研发项目(编号:2024SHFZ29)
作者单位
王丽丽 032200 山西汾阳 山西省汾阳医院内分泌科 
田瑶 032200 山西汾阳 山西省汾阳医院内分泌科 
王峰云 032200 山西汾阳 山西省汾阳医院内分泌科 
王丽静 032200 山西汾阳 山西省汾阳医院内分泌科 
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中文摘要:
      目的 探讨亚临床甲减(SCH)合并肥胖患者血清鸢尾素、耐斯他汀-1/摄食抑制因子-1(NesfatiN-1)与动脉粥样硬化(AS)的关系。方法 回顾性分析2024年1月—2025年1月山西省汾阳医院内分泌科144例SCH患者的临床资料,根据是否合并肥胖分为肥胖组(n=86)和非肥胖组(n=58),选取同期健康体检者作为对照组(n=45)。比较三组患者血清鸢尾素、NesfatiN-1水平,并根据SCH患者是否发生AS进行再次分组,比较合并AS组、未合并AS组的临床资料,采用logistic回归分析SCH合并肥胖患者发生AS的影响因素,进一步采用受试者工作特征曲线(ROC)分析鸢尾素、NesfatiN-1评估SCH患者合并肥胖患AS风险的价值。结果 与对照组比较,肥胖组、非肥胖组血清鸢尾素升高、NesfatiN-1水平则降低,差异有统计学意义(P<0.05)。单因素分析结果中,与非肥胖组比较,肥胖组鸢尾素升高[(861.35±108.47)ng/mL比(759.62±99.85)ng/mL]、NesfatiN-1水平降低[(3.64±0.63)ng/mL比(4.50±0.71)ng/mL],体质量、TSH、LDL-C更高,差异有统计学意义(P<0.05)。多因素结果显示,SCH合并肥胖患者AS独立危险因素包括TSH、LDL-C、鸢尾素水平升高及NesfatiN-1水平降低(P<0.05);ROC结果显示,鸢尾素、NesfatiN-1对SCH合并肥胖患者出现AS风险的预测AUC值分别为0.767、0.841,联合预测AUC则为0.893,高于单独预测曲线下面积(AUC)(P<0.05)。结论 SCH合并肥胖患者血清鸢尾素水平升高,血清NesfatiN-1水平降低,且鸢尾素、NesfatiN-1水平与AS发生独立相关,能预测SCH合并肥胖患者AS的发生。
英文摘要:
      Objective To explore the relationship between serum irisin, Nesfatin-1 and atherosclerosis(AS) in patients with subclinical hypothyroidism(SCH) complicated with obesity. Methods A retrospective analysis was conducted on the clinical data of 144 patients with SCH enrolled in the Department of Endocrinology, Fenyang Hospital of Shanxi Province, from January 2024 to January 2025. According to the presence or absence of obesity, the patients were divided into the obese group(n=86) and non-obese group(n=58). Meanwhile, 45 healthy subjects undergoing physical examination were enrolled as the control group. The serum levels of irisin and Nesfatin-1 were compared among the three groups. SCH patients were re-grouped according to whether AS occurred, and the clinical data were compared between the AS group and non-AS group. Logistic regression analysis was used to analyze the influencing factors of AS in SCH patients complicated with obesity. Receiver operating characteristic(ROC) curve analysis was further performed to evaluate the predictive value of irisin and Nesfatin-1 for AS risk in this population. Results Compared with the control group, the obese group and non-obese group presented significantly increased serum irisin and decreased Nesfatin-1 levels(P<0.05). Univariate analysis showed that, compared with the non-obese group, the obese group had higher irisin [(861.35±108.47) ng/mL vs. (759.62±99.85) ng/mL], lower Nesfatin-1[(3.64±0.63) ng/mL vs. (4.50±0.71) ng/mL], as well as higher body mass, TSH and LDL-C, with statistically significant differences(P<0.05). Multivariate analysis indicated that elevated TSH, LDL-C and irisin, together with reduced Nesfatin-1, were independent risk factors for AS in SCH patients complicated with obesity(P<0.05). ROC analysis revealed that the AUC value of irisin and Nesfatin-1 in predicting AS risk was 0.767 and 0.841, respectively, and the combined predictive AUC reached 0.893, which was significantly higher than that of single index prediction(P<0.05). Conclusion The serum irisin level in patients with SCH complicated with obesity is significantly increased, and the serum NesfatiN-1 level is significantly decreased. Moreover, the levels of irisin and NesfatiN-1 are independently associated with the occurrence of AS, which can predict the occurrence of AS in patients with SCH complicated with obesity.
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