Association of urinary C-megalin with albuminuria and renal function in diabetes: a cross-sectional study (Diabetes Distress and Care Registry at Tenri [DDCRT 21])

被引:5
作者
Kurita, Noriaki [1 ,2 ,3 ,4 ]
Kinoshita, Maki [5 ]
Fujimura, Maki [6 ]
Kurosawa, Kentaro [6 ]
Sakuramachi, Yui [6 ]
Takano, Kiyoko [6 ]
Okamura, Shintaro [6 ]
Kitatani, Mako [6 ]
Tsujii, Satoru [6 ]
Norton, Edward C. [7 ]
Hayashino, Yasuaki [6 ]
机构
[1] Fukushima Med Univ, Grad Sch Med, Dept Clin Epidemiol, 1 Hikarigaoka, Fukushima, Fukushima 9601295, Japan
[2] Fukushima Med Univ Hosp, Dept Innovat Res & Educ Clinicians & Trainees DiR, Fukushima, Japan
[3] Fukushima Med Univ, Ctr Innovat Res Commun & Clin Excellence CIRC2LE, Fukushima, Japan
[4] Inst Hlth Outcomes & Proc Evaluat Res iHope Int, Kyoto, Japan
[5] Tenri Hosp, Dept Clin Lab, Nara, Japan
[6] Tenri Hosp, Dept Endocrinol, Nara, Japan
[7] Univ Michigan, Sch Publ Hlth, Dept Hlth Management & Policy, Ann Arbor, MI 48109 USA
基金
日本学术振兴会;
关键词
C-megalin; Diabetes; Diabetic kidney disease; Biomarker; Renal function; PROSPECTIVE COHORT; PROTEIN; MICROALBUMINURIA; NEPHROPATHY; DIAGNOSIS;
D O I
10.1007/s40620-021-00995-2
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
Background A urinary biomarker sensitive to glomerular functional or structural changes in diabetic kidney disease is required. This study examined whether urinary C-megalin reflects renal function or albuminuria in diabetes. Methods This was a cross-sectional study involving 1576 patients with type 1 or 2 diabetes. The exposure variables were estimated glomerular filtration rate (eGFR) and urinary albumin-to-creatinine ratio (UACR), and the outcomes were urinary C-megalin excretion and concentration. Two-part models were used to examine the associations between eGFR and UACR with urinary C-megalin excretion or concentration. Results The UACR was linearly associated with urinary C-megalin excretion (per 100 mg/gCr of UACR; 11.8 fM/gCr [95% CI 8.9-14.7]). There was no association between decreasing eGFR and increasing urinary C-megalin excretion. The UACR was also linearly associated with the urinary C-megalin concentration (per 100 mg/gCr of UACR, 7.7 fM/L [95% CI 5.8-9.6]). At eGFR values > 60 mL/min/1.73 m(2), the eGFR and urinary C-megalin concentration were inversely linearly related (per 10 mL/min/1.73 m(2) decline, 7.7 fM/L [95% CI 0.2-15.1]). Conclusion Urinary C-megalin excretion as well as concentration levels are potentially useful biomarkers to detect early changes in diabetic kidney disease.
引用
收藏
页码:201 / 210
页数:10
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