Department of Pharmaceutical Biochemistry, Faculty of Medicine, Pharmacy and Dentistry, Cheikh Anta Diop University, Dakar, Senegal.
Albert Royer National University Hospital of Children, Dakar, Senegal.
PLoS One. 2022 Nov 21;17(11):e0273745. doi: 10.1371/journal.pone.0273745. eCollection 2022.
Sickle cell anemia (SCA) is caused by a single point variation in the β-globin gene (HBB): c.20A> T (p.Glu7Val), in homozygous state. SCA is characterized by sickling of red blood cells in small blood vessels which leads to a range of multiorgan complications, including kidney dysfunction. This case-control study aims at identifying sickle cell nephropathy biomarkers in a group of patients living with SCA from Senegal. A total of 163 patients living with SCA and 177 ethnic matched controls were investigated. Biological phenotyping included evaluation of glycemia, glucosuria, albuminuria, proteinuria, tubular proteinuria, serum creatinine, urine creatinine, urine specific gravity and glomerular filtration rate. Descriptive statistics of biomarkers were performed using the χ2 -test, with the significance level set at p<0.05. Patients living with SCA had a median age of 20 years (range 4 to 57) with a female sex frequency of 53.21%. The median age of the control participants was 29 years (range: 4-77) with a female sex frequency of 66.09%. The following proportions of abnormal biological indices were observed in SCA patients versus (vs.) controls, as follows: hyposthenuria: 35.3%vs.5.2% (p<0.001); glomerular hyperfiltration: 47.66%vs.19.75% (p<0.001), renal insufficiency: 5.47%vs.3.82% (p = 0.182); microalbuminuria: 42.38%vs.5.78% (p<0.001); proteinuria: 39.33%vs.4.62% (p<0.001); tubular proteinuria: 40.97%vs.4.73% (p<0.001) and microglucosuria: 22.5%vs.5.1% (p<0.001). This study shows a relatively high proportion of SCA nephropathy among patients living with SCA in Senegal. Microglucosuria, proteinuria, tubular proteinuria, microalbuminuria, hyposthenuria and glomerular hyperfiltration are the most prevalent biomarkers of nephropathy in this group of Senegalese patients with SCA.
镰状细胞贫血症(SCA)是由β-珠蛋白基因(HBB)中的单个点变异引起的:c.20A>T(p.Glu7Val),纯合状态。SCA 的特征是红细胞在小血管中镰状化,导致一系列多器官并发症,包括肾功能障碍。本病例对照研究旨在确定来自塞内加尔的一组 SCA 患者中的镰状细胞肾病生物标志物。共调查了 163 名 SCA 患者和 177 名种族匹配的对照者。生物学表型包括血糖、糖尿、白蛋白尿、蛋白尿、管状蛋白尿、血清肌酐、尿肌酐、尿比重和肾小球滤过率的评估。使用 χ2-检验对生物标志物进行描述性统计,显著性水平设为 p<0.05。SCA 患者的中位年龄为 20 岁(范围为 4 至 57 岁),女性频率为 53.21%。对照参与者的中位年龄为 29 岁(范围:4-77 岁),女性频率为 66.09%。与对照组相比,SCA 患者存在以下异常生物指标的比例如下:低渗尿:35.3%vs.5.2%(p<0.001);肾小球高滤过:47.66%vs.19.75%(p<0.001),肾功能不全:5.47%vs.3.82%(p=0.182);微量白蛋白尿:42.38%vs.5.78%(p<0.001);蛋白尿:39.33%vs.4.62%(p<0.001);管状蛋白尿:40.97%vs.4.73%(p<0.001);微量糖尿:22.5%vs.5.1%(p<0.001)。本研究显示塞内加尔 SCA 患者中 SCA 肾病的比例相对较高。微量糖尿、蛋白尿、管状蛋白尿、微量白蛋白尿、低渗尿和肾小球高滤过是该组塞内加尔 SCA 患者中最常见的肾病生物标志物。