Clinic for Nephrology and Rheumatology, University Medical Center Göttingen, Göttingen, Germany.
Institute of Human Genetics, Klinikumrechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Clin Genet. 2021 Jan;99(1):143-156. doi: 10.1111/cge.13861. Epub 2020 Oct 25.
Early initiation of therapy in patients with Alport syndrome (AS) slows down renal failure by many years. Genotype-phenotype correlations propose that the location and character of the individual's variant correlate with the renal outcome and any extra renal manifestations. In-depth clinical and genetic data of 60/62 children who participated in the EARLY PRO-TECT Alport trial were analyzed. Genetic variants were interpreted according to current guidelines and criteria. Genetically solved patients with X-linked inheritance were then classified according to the severity of their COL4A5 variant into less-severe, intermediate, and severe groups and disease progress was compared. Almost 90% of patients were found to carry (likely) pathogenic variants and classified as genetically solved cases. Patients in the less-severe group demonstrated a borderline significant difference in disease progress compared to those in the severe group (p = 0.05). While having only limited power according to its sample size, an obvious strength is the precise clinical and genetic data of this well ascertained cohort. As in published data differences in clinical progress were shown between patients with COL4A5 less-severe and severe variants. Therefore, clinical and segregational data are important for variant (re)classification. Genetic testing should be mandatory allowing early diagnosis and therapy of AS.
早期启动治疗可使 Alport 综合征(AS)患者的肾功能衰竭延缓多年。基因型-表型相关性研究表明,个体变异的位置和特征与肾脏结局和任何肾脏外表现相关。对参与 EARLY PROTECT Alport 试验的 60/62 名儿童的深入临床和遗传数据进行了分析。根据当前的指南和标准对遗传变异进行解释。然后,根据 COL4A5 变异的严重程度,将 X 连锁遗传的基因解决患者分为轻度、中度和重度组,并比较疾病进展情况。几乎 90%的患者携带(可能)致病性变异,并被归类为基因解决病例。与严重组相比,轻度组患者的疾病进展有边缘显著差异(p=0.05)。尽管根据其样本量,其结果仅具有有限的说服力,但该研究的优势在于该确定队列具有精确的临床和遗传数据。正如已发表的数据所示,COL4A5 轻度和重度变异患者的临床进展存在差异。因此,临床和遗传数据对于变异(重新)分类很重要。遗传检测应作为强制性要求,以实现 AS 的早期诊断和治疗。