SUIT, secretory units of islets in transplantation: An index for therapeutic management of islet transplanted patients and its application to type 2 diabetes

被引:69
作者
Yamada, Yuichiro
Fukuda, Kazuhito
Fujimoto, Shimpei
Masaya, Hosokawa
Tsukiyama, Katsushi
Nagashima, Kazuaki
Fukushima, Mitsuo
Suzuki, Haruhiko
Toyoda, Kentaro
Sassa, Mariko
Funakoshi, Shogo
Inagaki, Nobuya
Taniguchi, Ataru
Sato, T. Shun
Matsumoto, Shinichi
Tanaka, Koichi
Seino, Yutaka
机构
[1] Kyoto Univ, Grad Sch Med, Dept Diabet & Clin Nutr, Sakyo Ku, Kyoto 6068507, Japan
[2] Kansai Elect Power Hosp, Osaka, Japan
[3] Kyoto Univ, Sch Publ Hlth, Dept Biostat, Kyoto, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Transplantat & Immunol, Sakyo Ku, Kyoto 6068507, Japan
关键词
islet transplantation; insulin; diabetes;
D O I
10.1016/j.diabres.2006.03.030
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Evaluation of a patient's pancreatic beta-cell function is important in both diagnosis and treatment of diabetes. We sought to determine beta-cell function with a single sampling of blood. Examination of fasting blood glucose (F-BG, mM) and C-peptide (FCPR, nM) levels in seven post-islet-transplanted states of four patients revealed a linear relationship between F-BG and F-CPR. Assuming that normal subjects aged < 40 years have 100% pancreatic beta-cell function, we developed the secretory units of islets in transplantation (SUIT) as an index of beta-cell function by the formula: 250 x F-CPR/(F-BG - 3.43). The SUIT index was correlated with the stimulated C-peptide levels not only in islet-transplanted patients (R-2 = 0.68, P < 0.05) but also in type 2 patients (R-2 = 0.34, P < 0.001). Since the SUIT index can be calculated from data obtained at a single fasting blood sampling and predict the pancreatic beta-cell function, the formula may be a useful tool in clinical management of diabetes. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:222 / 226
页数:5
相关论文
共 20 条
[1]
Glucokinase mutations, insulin secretion, and diabetes mellitus [J].
Bell, GI ;
Pilkis, SJ ;
Weber, IT ;
Polonsky, KS .
ANNUAL REVIEW OF PHYSIOLOGY, 1996, 58 :171-+
[2]
PHYSIOLOGIC EVALUATION OF FACTORS CONTROLLING GLUCOSE-TOLERANCE IN MAN - MEASUREMENT OF INSULIN SENSITIVITY AND BETA-CELL GLUCOSE SENSITIVITY FROM THE RESPONSE TO INTRAVENOUS GLUCOSE [J].
BERGMAN, RN ;
PHILLIPS, LS ;
COBELLI, C .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (06) :1456-1467
[3]
β-cell deficit and increased β-cell apoptosis in humans with type 2 diabetes [J].
Butler, AE ;
Janson, J ;
Bonner-Weir, S ;
Ritzel, R ;
Rizza, RA ;
Butler, PC .
DIABETES, 2003, 52 (01) :102-110
[4]
DCCT Res Grp, 1987, J CLIN ENDOCR METAB, V65, P30
[5]
DEFRONZO RA, 1979, AM J PHYSIOL, V237, P214
[7]
Increased islet apoptosis in Pdx1+/- mice [J].
Johnson, JD ;
Ahmed, NT ;
Luciani, DS ;
Han, ZQ ;
Tran, H ;
Fujita, J ;
Misler, S ;
Edlund, H ;
Polonsky, KS .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (08) :1147-1160
[8]
Alterations in the glucose-stimulated insulin secretory dose-response curve and in insulin clearance in nondiabetic insulin-resistant individuals [J].
Jones, CNO ;
Pei, D ;
Staris, P ;
Polonsky, KS ;
Chen, YDI ;
Reaven, GM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (06) :1834-1838
[9]
Insulin independence after living-donor distal pancreatectomy and islet allotransplantation [J].
Matsumoto, S ;
Okitsu, T ;
Wanaga, Y ;
Noguchi, H ;
Nagata, H ;
Yonekawa, Y ;
Yamada, Y ;
Fukuda, K ;
Tsukiyama, K ;
Suzuki, H ;
Kawasaki, Y ;
Shimodaira, M ;
Matsuoka, K ;
Shibata, T ;
Kasai, Y ;
Maekawa, T ;
Shapiro, AMJ ;
Tanaka, K .
LANCET, 2005, 365 (9471) :1642-1644
[10]
Effect of the two-layer (University of Wisconsin solution-perfluorochemical plus O2) method of pancreas preservation on human islet isolation, as assessed by the Edmonton isolation protocol [J].
Matsumoto, S ;
Qualley, SA ;
Goel, S ;
Hagman, DK ;
Sweet, IR ;
Poitout, V ;
Strong, DM ;
Robertson, RP ;
Reems, JA .
TRANSPLANTATION, 2002, 74 (10) :1414-1419