Division of Paediatric Rheumatology, Department of Paediatrics, Schulich School of Medicine & Dentistry, University of Western Ontario, 800 Commissioners Rd E. B1-146, London, ON, N6A 5W9, Canada.
Department of Pediatric Rheumatology, ASST G Pini, Milano, Italy.
Sci Rep. 2020 Oct 27;10(1):18374. doi: 10.1038/s41598-020-75433-7.
Chronic inflammation and proteinuria is a risk factor for cardiovascular disease (CVD) in patients with chronic kidney diseases and rheumatologic disorders. Our aim was to investigate the CVD events (CVDEs) and survival between the patients with FMF-related AA amyloidosis and glomerulonephropathies (GN) to define possible predictors for CVDEs. A prospective follow-up study with FMF-amyloidosis and glomerulonephropathy (GN) was performed and patients were followed for CVDEs. Flow-mediated dilatation (FMD), FGF-23, serum lipid, hsCRP levels, BMI and HOMA were assessed. A Cox regression analysis was performed to evaluate the risk factors for CVDEs. There were 107 patients in the FMF-amyloidosis group and 126 patients with GN group. Forty-seven CVDEs were observed during the 4.2-years follow up; all 28 patients in the FMF-amyloidosis group and 14/19 patients with GN developed CVDEs before the age of 40 (p = 0.002). CVD mortality was 2.8 times higher (95% CI 1.02-7.76) in patients with FMF-amyloidosis. Across both groups, FMD and FGF23 (p < 0.001) levels were independently associated with the risk of CVDEs. Patients with FMF-amyloidosis are at increased risk of early CVDEs with premature mortality age. FGF 23, FMD and hsCRP can stratify the risk of early CVD in patients with FMF-related AA amyloidosis.
慢性炎症和蛋白尿是慢性肾脏疾病和风湿性疾病患者心血管疾病(CVD)的危险因素。我们的目的是研究家族性地中海热相关淀粉样变和肾小球肾炎(GN)患者的 CVD 事件(CVDEs)和存活率,以确定 CVDEs 的可能预测因素。对家族性地中海热相关淀粉样变和肾小球肾炎(GN)进行了前瞻性随访研究,并对患者进行了 CVDEs 的随访。评估了血流介导的扩张(FMD)、FGF-23、血清脂质、hsCRP 水平、BMI 和 HOMA。进行 Cox 回归分析以评估 CVDEs 的危险因素。在家族性地中海热相关淀粉样变组中有 107 例患者,在 GN 组中有 126 例患者。在 4.2 年的随访中观察到 47 例 CVDEs;家族性地中海热相关淀粉样变组中所有 28 例患者和 GN 组中 14/19 例患者在 40 岁之前发生 CVDEs(p=0.002)。家族性地中海热相关淀粉样变组的 CVD 死亡率是 GN 组的 2.8 倍(95%CI 1.02-7.76)。在两组中,FMD 和 FGF23(p<0.001)水平均与 CVDEs 的风险独立相关。家族性地中海热相关淀粉样变患者发生早期 CVDEs 的风险增加,且死亡年龄较早。FGF 23、FMD 和 hsCRP 可分层家族性地中海热相关 AA 淀粉样变患者早期 CVD 的风险。