Growth Differentiation Factor-15 and Risk of CKD Progression

被引:139
|
作者
Nair, Viji [1 ]
Robinson-Cohen, Cassianne [4 ]
Smith, Michelle R. [1 ]
Bellovich, Keith A. [5 ]
Bhat, Zeenat Yousuf [6 ]
Bobadilla, Maria [7 ]
Brosius, Frank [1 ]
de Boer, Ian H. [4 ]
Essioux, Laurent [8 ]
Formentini, Ivan [8 ,11 ]
Gadegbeku, Crystal A. [9 ]
Gipson, Debbie [2 ]
Hawkins, Jennifer [1 ]
Himmelfarb, Jonathan [4 ]
Kestenbaum, Bryan [4 ]
Kretzler, Matthias [1 ,3 ]
Magnone, Maria Chiara [8 ,11 ]
Perumal, Kalyani [10 ]
Steigerwalt, Susan [2 ]
Ju, Wenjun [1 ,3 ]
Bansal, Nisha [4 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Nephrol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Pediat, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
[4] Univ Washington, Kidney Res Inst, Div Nephrol, Seattle, WA 98104 USA
[5] St Clair Nephrol Res, Div Nephrol, Detroit, MI USA
[6] Wayne State Univ, Dept Internal Med, Div Nephrol, Detroit, MI 48202 USA
[7] F Hoffmann La Roche, Roche Partnering, Basel, Switzerland
[8] Roche Innovat Ctr Basel, Discovery Biol Pharmaceut Sci, Roche Pharmaceut Res & Early Dev, Basel, Switzerland
[9] Temple Univ, Dept Med, Sch Med, Philadelphia, PA 19122 USA
[10] John H Stroger Jr Hosp Cook Cty, Chicago, IL USA
[11] AstraZeneca, Cardiovasc & Metab Dis Innovat Med, Pepparedsleden 1, Molndal, Sweden
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2017年 / 28卷 / 07期
基金
美国国家卫生研究院;
关键词
CHRONIC KIDNEY-DISEASE; MYOCARDIAL-INFARCTION; ALL-CAUSE; MORTALITY; HEART; ATHEROSCLEROSIS; ASSOCIATION; BIOMARKERS; PROTECTS; MARKER;
D O I
10.1681/ASN.2016080919
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Growth differentiation factor-15 (GDF-15) is a member of the TGF-beta cytokine superfamily that is widely expressed and may be induced in response to tissue injury. Elevations in GDF-15may identify a novel pathway involved in loss of kidney function among patients with CKD. Among participants in the Clinical Phenotyping and Resource Biobank (C-PROBE) study and the Seattle Kidney Study (SKS), we tested whether kidney tissue expression ofGDF15mRNA correlates with circulating levels of GDF-15 and whether elevations in circulating GDF-15 are associated with decline in kidney function. In matching samples of 24 patients with CKD from the C-PROBE study, circulating GDF-15 levels significantly correlated with intrarenal GDF15 transcript levels (r=0.54, P=0.01). Among the 224 C-PROBE and 297 SKS participants, 72 (32.1%) and 94 (32.0%) patients, respectively, reached a composite end point of 30% decline in eGFR or progression to ESRD over a median of 1.8 and 2.0 years of follow up, respectively. In multivariable models, after adjusting for potential confounders, every doubling of GDF-15 level associated with a 72% higher (95% confidence interval, 1.21 to 4.45; P=0.003) and 65% higher (95% confidence interval, 1.08 to 2.50; P=0.02) risk of progression of kidney disease in C-PROBE and SKS participants, respectively. These results show that circulating GDF-15 levels strongly correlated with intrarenal expression of GDF15 and significantly associated with increased risk of CKD progression in two independent cohorts. Circulating GDF-15may be a marker for intrarenal GDF15-related signaling pathways associated with CKD and CKD progression.
引用
收藏
页码:2233 / 2240
页数:8
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