A model to predict a risk of allergic rhinitis based on mitochondrial DNA copy number

被引:2
作者
Yuan, Huajie [1 ]
Su, Jiang [1 ]
Wang, Song [1 ]
Wang, Lingling [1 ]
Zhou, Wei [1 ]
Zhang, Bo [1 ]
Yan, Haisu [1 ]
Yang, Yuping [1 ]
Zhang, Hua [1 ]
机构
[1] Xinjiang Med Univ, Dept Otolaryngol, Affiliated Hosp 1, 137 Liyushan Ave, Urumqi 830054, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Allergic rhinitis; Nomogram; Asthma; Mitochondrial DNA copy number; Mitochondrial dysfunction; GENE-EXPRESSION; AIRWAY; SENSITIVITY; ASSOCIATION; NOMOGRAM; DISEASE;
D O I
10.1007/s00405-022-07341-7
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Purpose To determine whether mitochondrial DNA copy number (mtDNA-CN) is associated with allergic rhinitis (AR), and further establish a nomogram model for the early diagnosis of AR. Methods We carried out a case-control study involving a total of 134 subjects, including 66 healthy controls and 68 AR patients. The mtDNA-CN in peripheral blood of all subjects was detected by real-time fluorescence quantitative polymerase chain reaction, and general information of patients was recorded. And, least absolute shrinkage selection operator (LASSO) regression was used to screen clinically significant variables, which were substituted into a logistic regression analysis to determine independent risk factors. Next, a nomogram model was developed for the risk prediction of AR. Then, internal validation was performed with the bootstrap resampling. Ultimately, the clinical benefit and validity of the nomogram were assessed by receiver operating characteristic (ROC) curve, bias-corrected curve, and decision curve analysis (DCA). Results MtDNA-CN and total IgE were determined as independent risk factors of AR. The final model achieved an area under the ROC curve (AUC) of 0.869, and the DCA curve demonstrated that the nomogram was clinically beneficial for practical application. Conclusion An increase of the mtDNA-CN was linked to the occurrence risk of AR. The nomogram prediction model based on mtDNA-CN showed the potential clinical utility in improving risk prediction and providing new insights for exploring the pathogenesis of AR.
引用
收藏
页码:4997 / 5008
页数:12
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