Sheyyab Ahmed, Wahdan Rania, Al-Aitan Al-Ameen, Abukhadra Mahmoud, Ayed Naimat Laith Hussein
Department of Internal Medicine, Hashemite University Faculty of Medicine, Zarqa, Jordan.
Laboratory of Genetics, Prince Hamzah Hospital, Ministry of Health, Amman, Jordan.
Eurasian J Med. 2024 Sep 24;56(3):153-158. doi: 10.5152/eurasianjmed.2024.24457.
Familial Mediterranean Fever (FMF) is an inherited autosomal recessive disorder resulting from the inheritance of MEFV gene mutations. Patients with FMF are at increased risk of secondary amyloidosis, namely type AA. In some Mediterranean populations, the α genotype was associated with the development of renal amyloidosis, a finding not reproduced in other populations. Our study aimed to assess the association of SAA1 genotypes with renal involvement. This is a retrospective analysis of FMF patients which were followed at our institute between January 2016 and August 2022. Familial Mediterranean Fever screening was performed using polymerase chain reaction and reverse hybridization techniques. Statistical analysis was performed using bivariate logistic regression. MEFV analysis of the studied patients (n=427) identified 52 patients with a homozygous genotype (12.1%) and 374 with a heterozygous genotype (87.5%). The heterozygous group were mostly heterozygous carriers of a single FMF variant (81%), while 19% were compound heterozygous. Renal involvement was revealed in 95 patients (22.2%), which were manifested as proteinuria (21.3%) and/or renal impairment in 4 patients (3%). The clinical diagnosis of amyloidosis was suspected in 6 patients only (1.4%). Analysis for SAA1 gene genotype-phenotype correlation showed that patients with the SAA1.1/1.1 (OR=0.54, P=.452) was not statistically associated with renal involvement. Pearson Chi-square was performed to examine the association between FMF homozygosity and each SAA1 genotype, which showed a significant association between FMF gene homozygosity with SAA1.1/1.1 genotype (χ2 = 8.06, P=.018). In our Jordanian FMF population, we report low rates of renal involvement with a high rate of the β haplotype (SAA1.5). Neither the α/α nor the β/β genotypes were associated with evidence of renal involvement.
家族性地中海热(FMF)是一种常染色体隐性遗传病,由MEFV基因突变遗传所致。FMF患者发生继发性淀粉样变性(即AA型)的风险增加。在一些地中海人群中,α基因型与肾淀粉样变性的发生有关,但这一发现未在其他人群中得到验证。我们的研究旨在评估SAA1基因型与肾脏受累之间的关联。这是一项对2016年1月至2022年8月在我们研究所随访的FMF患者进行的回顾性分析。采用聚合酶链反应和反向杂交技术进行家族性地中海热筛查。使用双变量逻辑回归进行统计分析。对427例研究患者进行的MEFV分析发现,52例患者为纯合基因型(12.1%),374例为杂合基因型(87.5%)。杂合组大多是单一FMF变异的杂合携带者(81%),而19%为复合杂合子。95例患者(22.2%)出现肾脏受累,表现为蛋白尿(21.3%)和/或4例患者(3%)出现肾功能损害。仅6例患者(1.4%)临床怀疑为淀粉样变性。SAA1基因基因型-表型相关性分析显示,SAA1.1/1.1患者(OR=0.54,P=0.452)与肾脏受累无统计学关联。采用Pearson卡方检验来检验FMF纯合性与每种SAA1基因型之间关联,结果显示FMF基因纯合性与SAA1.1/1.1基因型之间存在显著关联(χ2 = 8.06,P=0.018)。在我们约旦的FMF人群中,我们报告肾脏受累率较低,β单倍型(SAA1.5)发生率较高。α/α和β/β基因型均与肾脏受累证据无关。