Wafaa Ahmed Shehata, Mostafa Ahmed Hammam, Aya Abdo, Nermin Tayel, Shimaa Abdelsattar
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引用次数: 0
摘要
斑秃(AA)是一种有多种病因的疾病。有证据表明,线粒体脱氧核糖核酸(mtDNA)的绝对拷贝数以及突变mtDNA拷贝的比例决定了疾病的发生。本研究旨在量化AA患者和健康对照者mtDNA拷贝数的相对指标,并将结果与现有临床信息相关联。本病例对照研究包括50例AA患者和50例年龄和性别一致的健康人作为对照。AA的严重程度采用脱发严重程度评分法和Kavak分级法进行加权。实时荧光定量pcr检测mtDNA拷贝数的相对指标。病例与对照组mtDNA拷贝数差异有统计学意义(p p = 0.001)。临界值>1.619 N/µL可显著诊断AA (p = 1.36 N/µL可区分轻度AA和中度AA, p = 0.007)。mtDNA拷贝数相对指标在AA患者中显著升高,可用于诊断和评价AA的严重程度。
Mitochondrial DNA copy number as a diagnostic marker and indicator of degree of severity in alopecia areata.
Alopecia areata (AA) is a disorder with several etiologies. The evidence suggests that the absolute copy number of mitochondrial deoxyribonucleic acid (mtDNA), as well as proportion of mutated mtDNA copies, determines disease onset. This study aims to quantify the relative index of the mtDNA copy number in patients with AA and healthy controls and correlate the results with the existing clinical information. This case-control study included 50 patients with AA and 50 age- and sex-coordinated healthy persons as controls. The severity of AA was weighed using the Severity of Alopecia Tool and Kavak's classification. The relative index of the mtDNA copy number was measured by real-time qPCR. Significant statistical difference was observed between cases and controls regarding mean mtDNA copy number, p < .001. There was significant positive correlation with SALT score (p = 0.001). A cutoff value of >1.619 N/µL could significantly diagnose AA cases (p < .001), and a cutoff value of > 1.36 N/µL could discriminate mild AA cases from those with moderate AA (p = 0.007). The relative index of mtDNA copy number is significantly elevated in AA cases and could be helpful in diagnosing and evaluating AA severity.
期刊介绍:
The Journal of Immunoassay & Immunochemistry is an international forum for rapid dissemination of research results and methodologies dealing with all aspects of immunoassay and immunochemistry, as well as selected aspects of immunology. They include receptor assay, enzyme-linked immunosorbent assay (ELISA) in all of its embodiments, ligand-based assays, biological markers of ligand-receptor interaction, in vivo and in vitro diagnostic reagents and techniques, diagnosis of AIDS, point-of-care testing, clinical immunology, antibody isolation and purification, and others.