Sickle cell trait, estimated glomerular filtration rate, and risk of adverse outcomes in chronic kidney disease.
Sickle cell trait, estimated glomerular filtration rate, and risk of adverse outcomes in chronic kidney disease.
复制标题
镰状细胞性状、估计肾小球滤过率以及慢性肾脏病不良后果的风险。
DOI:
10.1002/ajh.25588
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发表时间:
2019
影响因子:
12.8
通讯作者:
Naik,RakhiP
中科院分区:
文献类型:
--
作者:
Sood,Rupali;Surapaneni,Aditya;Luo,Shengyuan;Appel,LawrenceJ;Winkler,Cheryl;Grams,MorganE;Naik,RakhiP
Recent evidence suggests that sickle cell trait (SCT), defined as the heterozygous inheritance of sickle hemoglobin, is associated with an increased risk of prevalent and incident chronic kidney disease (CKD). 1, 2 However, there is limited evidence as to whether SCT is associated with an increased risk of other relevant outcomes, including cardiovascular disease (CVD), CKD progression, end-stage kidney disease (ESKD), and death among those with established CKD. 1 Determining risk for these outcomes is important since referrals for nephrology care, vascular access, and transplant are largely based on the probability of adverse outcomes. Another complicating aspect of the study of CKD and SCT is the concern that serum creatinine as a filtration marker may poorly reflect true GFR for patients with sickle cell anemia due to non-GFR determinants; 3 however, the performance of creatinine in SCT is unknown. Among participants in the African American Study of Kidney Disease and Hypertension (AASK) study, a well-characterized cohort of individuals with hypertensionattributed CKD followed for a median of 10 years, we evaluated the accuracy and precision of GFR measured by 125I-iothalamate (mGFR) compared to creatinine-based GFR estimates