Department of Nephrology, Ochsner Health System, New Orleans, Louisiana, USA.
Ochsner Clinical School, The University of Queensland, Brisbane, Queensland, Australia.
Kidney Blood Press Res. 2022;47(9):586-591. doi: 10.1159/000522081. Epub 2022 May 24.
It has been noted in observational and interventional studies that individuals exposed to fenofibrate can exhibit a rise in serum creatinine (sCr) concentration. However, it is not known to what extent this phenomenon impacts kidney function in patients who are referred to a nephrology clinic for consultation for chronic kidney disease (CKD).
We conducted a prospective observational study of patients referred to our nephrology clinic for a new evaluation of a rise in sCr or worsening CKD and who were on fenofibrate therapy. We examined the effect of discontinuation of fenofibrate on kidney function, change in sCr, and estimated glomerular filtration (eGFR) at 3, 6, and 12 months.
A total of 22 patients (59% women, 86% White, 59% with type 2 diabetes, and 18% with peripheral arterial disease) were captured over 2.5 years. Median sCr at the time of fenofibrate discontinuation was 1.9 (1.1-3.3) mg/dL and eGFR, 32 (17-57) mL/min; proteinuria was absent in 17 (77%). Upon discontinuation of fenofibrate, median sCr decreased to 1.5 (0.9-2.4), 1.4 (1.0-2.5), and 1.4 (1.0-2.3) mg/dL at 3, 6, and 12 months, respectively (p < 0.05); whereas median eGFR increased to 44 (27-71), 45 (23-71), and 42 (21-71) mL/min, respectively (p < 0.05). A ≥30% rise in eGFR was observed in 59% of the patients at 3 months, and it persisted in 45% and 50% of patients at 6 and 12 months, respectively.
Discontinuation of fenofibrate in patients referred for CKD evaluation can result in sustained reduction in sCr in about half of the patients and for up to 1 year. There is a need to raise awareness among primary practitioners about this phenomenon. Recognition of fenofibrate as a cause of rise in sCr could reduce unnecessary nephrology consultation and resource utilization.
在观察性和干预性研究中,已经注意到接触非诺贝特的个体可能会出现血清肌酐(sCr)浓度升高。然而,目前尚不清楚这种现象在因慢性肾脏病(CKD)就诊于肾病科的患者中对肾功能的影响程度。
我们对因 sCr 升高或 CKD 恶化而就诊于我院肾病科进行新评估并正在服用非诺贝特的患者进行了前瞻性观察性研究。我们检查了停用非诺贝特对肾功能、sCr 变化和肾小球滤过率(eGFR)的影响,分别在 3、6 和 12 个月时进行评估。
在 2.5 年期间共捕获了 22 名患者(59%为女性,86%为白人,59%患有 2 型糖尿病,18%患有外周动脉疾病)。停用非诺贝特时的 sCr 中位数为 1.9(1.1-3.3)mg/dL,eGFR 中位数为 32(17-57)mL/min;17 名(77%)患者无蛋白尿。停用非诺贝特后,sCr 中位数分别在 3、6 和 12 个月时降至 1.5(0.9-2.4)、1.4(1.0-2.5)和 1.4(1.0-2.3)mg/dL(p<0.05);eGFR 中位数分别增至 44(27-71)、45(23-71)和 42(21-71)mL/min(p<0.05)。3 个月时,59%的患者 eGFR 升高≥30%,在 6 个月和 12 个月时,分别有 45%和 50%的患者持续出现该现象。
在因 CKD 评估而就诊的患者中停用非诺贝特可导致约一半患者的 sCr 持续降低,最长可持续 1 年。需要提高初级保健医生对这一现象的认识。认识到非诺贝特是 sCr 升高的原因,可以减少不必要的肾病科咨询和资源利用。