Insulin-Like Growth Factor Binding Protein 7 Predicts Renal and Cardiovascular Outcomes in the Canagliflozin Cardiovascular Assessment Study

被引:17
作者
Januzzi Jr, James L. [1 ,2 ]
Butler, Javed [3 ]
Sattar, Naveed [4 ]
Xu, Jialin [5 ]
Shaw, Wayne [6 ]
Rosenthal, Norman [6 ]
Pfeifer, Michael [7 ]
Mahaffey, Kenneth W. [8 ]
Neal, Bruce [9 ,10 ,11 ]
Hansen, Michael K.
机构
[1] Massachusetts Gen Hosp, Cardiol Div, Boston, MA 02114 USA
[2] Baim Inst Clin Res, Boston, MA USA
[3] Univ Mississippi, Jackson, MS 39216 USA
[4] Glasgow Cardiovasc Res, Glasgow, Lanark, Scotland
[5] Janssen Res & Dev LLC, Spring House, PA USA
[6] Janssen Res & Dev LLC, Raritan, NJ USA
[7] Janssen Sci Affairs LLC, Titusville, NJ USA
[8] Stanford Univ, Dept Med, Sch Med, Stanford Ctr Clin Res, Stanford, CA 94305 USA
[9] Univ Sydney, George Inst Global Hlth, Sydney, NSW, Australia
[10] Univ Sydney, Charles Perkins Ctr, Sydney, NSW, Australia
[11] Imperial Coll London, London, England
关键词
BASE-LINE CHARACTERISTICS; HEART-FAILURE; EJECTION FRACTION; BIOMARKER; RATIONALE; DESIGN;
D O I
10.2337/dc20-1889
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To analyze the association between concentrations of plasma insulin-like growth factor binding protein 7 (IGFBP7) with renal and cardiac outcomes among participants with type 2 diabetes and high cardiovascular risk. RESEARCH DESIGN AND METHODS Associations between IGFBP7 levels and clinical outcomes were assessed among participants in the Canagliflozin Cardiovascular Assessment Study (CANVAS) with type 2 diabetes and high cardiovascular risk. RESULTS Among CANVAS participants, 3,577 and 2,898 had IGFBP7 measured at baseline and 1 year, respectively. Per log-unit higher concentration, baseline IGFBP7 was significantly associated with the composite renal end point of sustained 40% reduction in estimated glomerular filtration rate, need for renal replacement therapy, or renal death (hazard ratio [HR] 3.51; P < 0.001) and the composite renal end point plus cardiovascular death (HR 4.90; P < 0.001). Other outcomes, including development or progression of albuminuria, were also predicted by baseline IGFBP7. Most outcomes were improved by canagliflozin regardless of baseline IGFBP7; however, those with baseline concentrations >= 96.5 ng/mL appeared to benefit more from canagliflozin relative to the first progression of albuminuria compared with those with lower baseline IGFBP7 (HR 0.64 vs. 0.95; P-interaction = 0.003). Canagliflozin did not lower IGFBP7 concentrations by 1 year; however, at 1 year, higher IGFBP7 concentrations more strongly predicted the composite renal end point (HR 15.7; P < 0.001). Patients with rising IGFBP7 between baseline and 1 year had the highest number of composite renal events. CONCLUSIONS Plasma IGFBP7 concentrations predicted renal and cardiac events among participants with type 2 diabetes and high cardiovascular risk. More data are needed regarding circulating IGFBP7 and progression of diabetic kidney disease and its complications.
引用
收藏
页码:210 / 216
页数:7
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