Urinary prostaglandin D synthase (β-trace) excretion increases in the early stage of diabetes mellitus

被引:46
作者
Hirawa, N
Uehara, Y
Ikeda, T
Gomi, T
Hamano, K
Totsuka, Y
Yamakado, M
Takagi, M
Eguchi, N
Oda, H
Seiki, K
Nakajima, H
Urade, Y
机构
[1] Maruha Corp, Cent Res Inst, Ibaraki, Osaka, Japan
[2] Osaka Biosci Inst, Dept Mol Behav Biol, Suita, Osaka 565, Japan
[3] Japan Sci & Technol Corp, Suita, Osaka, Japan
[4] Tokyo Police Hosp, Dept Med, Tokyo, Japan
[5] Mitsui Mem Hosp, Hlth Serv Ctr, Tokyo 101, Japan
[6] Nippon Telegraph & Tel Corp, Kanto Med Ctr, Dept Nephrol, Tokyo, Japan
[7] Nippon Telegraph & Tel Corp, Kanto Med Ctr, Dept Endocrinol & Metab, Tokyo, Japan
[8] Yokohama City Univ, Dept Med 2, Yokohama, Kanagawa 232, Japan
[9] Univ Tokyo, Hlth Serv Ctr, Tokyo, Japan
[10] Univ Tokyo, Dept Med 2, Bunkyo Ku, Tokyo 1130033, Japan
关键词
prostaglandin; prostaglandin D; prostaglandin D synthase; diabetes mellitus; proteinuria; kidney;
D O I
10.1159/000045937
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
Objective: Circulating levels of lipocalin-type prostaglandin D synthase (L-PGDS)/beta -trace reportedly increase in renal failure as well as in cardiovascular injuries. We investigated the alterations of L-PGDS in urine and plasma in the early stage of type-2 diabetic patients. Method: Thirty-six type-2 diabetic patients and 29 normal subjects were studied. Overnight spot urine and plasma samples were obtained in the morning. L-PGDS was measured by ELISA method using anti-L-PGDS antibody. Variables indicating renal function were determined. Results: Plasma L-PGDS concentration was slightly higher in the patients with diabetes mellitus than in the control subjects, whereas the urinary L-PGDS excretion almost doubled in the diabetic patients as compared with that in the control subjects. Plasma L-PGDS was determined by plasma creatinine (Cr) concentration while urinary L-PGDS excretion was correlated solely with urinary protein excretion. There was no relationship between plasma L-PGDS concentration and urinary L-PGDS excretion. The averaged plasma concentration of L-PGDS in the diabetics with a normal Cr level ill plasma, corresponding to that in the controls, was determined by the plasma Cr concentration. On the other hand, the urinary L-PGDS excretion was determined by the amount of proteinuria and greater in the diabetics with a normal Cr level in plasma than in the controls even when the patients exhibited urinary protein excretion equal to that in the control subjects. Conclusions: Urinary L-PGDS excretion increased in the early stage of kidney injury in patients with type-2 diabetes mellitus. The urinary excretion was correlated independently with urinary protein excretion even when there was no difference in urinary protein or albumin excretions, thereby suggesting that urinary L-PGDS excretion is possibly a more sensitive indicator of renal injuries than proteinuria. Urinary L-PGDS may thus predict the progression of renal injuries in diabetic patients. Copyright (C) 2001 S. Karger AG. Basel.
引用
收藏
页码:321 / 327
页数:7
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