Long-term clinical effects of epalrestat, an aldose reductase inhibitor, on progression of diabetic neuropathy and other microvascular complications: multivariate epidemiological analysis based on patient background factors and severity of diabetic neuropathy

被引:192
作者
Hotta, N. [1 ]
Kawamori, R. [2 ]
Fukuda, M. [3 ]
Shigeta, Y. [4 ]
机构
[1] Chubu Rosai Hosp, Nagoya, Aichi, Japan
[2] Juntendo Univ, Grad Sch Med, Sportol Ctr, Tokyo, Japan
[3] NTT W Osaka Hosp, Osaka, Japan
[4] Shiga Univ Med Sci, Otsu, Shiga 52021, Japan
关键词
SMOOTH-MUSCLE-CELLS; KINASE-C ACTIVATION; PERIPHERAL NEUROPATHY; DIAGNOSTIC-CRITERIA; PATHWAY; TARGET; RETINOPATHY;
D O I
10.1111/j.1464-5491.2012.03684.x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Diabet. Med. 29, 15291533 (2012) Abstract Aims The goal of the study was to evaluate the efficacy of epalrestat, an aldose reductase inhibitor, on diabetic retinopathy and diabetic nephropathy, based on analysis of the results of the Aldose Reductase InhibitorDiabetes Complications Trial, a 3-year multicentre comparative clinical trial of conventional therapy (control group) and epalrestat therapy (epalrestat group) in Japanese patients with mild diabetic neuropathy. Methods The subjects of the study were patients enrolled in the Aldose Reductase InhibitorDiabetes Complications Trial for whom data for major patient characteristics, severity of diabetic neuropathy at the end of the study and time-courses of diabetic retinopathy and diabetic nephropathy were available (57 and 52 patients from the control and epalrestat groups, respectively). Progression of diabetic retinopathy/nephropathy (a primary endpoint) in relation to major patient characteristics, severity of diabetic neuropathy at the end of the study (assessed from the mean of z-scores in four neurological function tests) and epalrestat treatment were analysed using univariate analysis and multiple logistic regression analysis. Results Progression of diabetic retinopathy/nephropathy was significantly inhibited in the epalrestat group compared with the control group (odds ratio = 0.323, P = 0.014) and was dependent on the severity of diabetic neuropathy at the end of the study (odds ratio = 2.131, P = 0.025). Conclusions Epalrestat prevented progression of diabetic neuropathy and retinopathy/nephropathy. The effect on diabetic retinopathy/nephropathy may have occurred indirectly because of the prevention of progression of diabetic neuropathy, in addition to the inhibitory action of epalrestat on aldose reductase.
引用
收藏
页码:1529 / 1533
页数:5
相关论文
共 31 条
[1]
[Anonymous], CURRENT DIAGNOSIS MA
[2]
Is peripheral neuropathy associated with retinopathy and albuminuria in individuals with impaired glucose metabolism? The 1999-2000 AusDiab [J].
Barr, ELM ;
Wong, TY ;
Tapp, RJ ;
Harper, CA ;
Zimmet, PZ ;
Atkins, R ;
Shaw, JE .
DIABETES CARE, 2006, 29 (05) :1114-1116
[3]
Response to comment on: American Diabetes Association. Standards of medical care in diabetes-2011 (vol 34, pg e54, 2011) [J].
Wysham, C. H. ;
Kirkman, M. S. .
DIABETES CARE, 2011, 34 (08) :1887-1887
[4]
Low Peripheral Nerve Conduction Velocities and Amplitudes Are Strongly Related to Diabetic Microvascular Complications in Type 1 Diabetes The EURODIAB Prospective Complications Study [J].
Charles, Morten ;
Soedamah-Muthu, Sabita S. ;
Tesfaye, Solomon ;
Fuller, John H. ;
Arezzo, Joseph C. ;
Chaturvedi, Nishi ;
Witte, Daniel R. .
DIABETES CARE, 2010, 33 (12) :2648-2653
[5]
PKC inhibition and diabetic microvascular complications [J].
Clarke, Margaret ;
Dodson, Paul M. .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 21 (04) :573-586
[6]
THE PREVALENCE BY STAGED SEVERITY OF VARIOUS TYPES OF DIABETIC NEUROPATHY, RETINOPATHY, AND NEPHROPATHY IN A POPULATION-BASED COHORT - THE ROCHESTER DIABETIC NEUROPATHY STUDY [J].
DYCK, PJ ;
KRATZ, KM ;
KARNES, JL ;
LITCHY, WJ ;
KLEIN, R ;
PACH, JM ;
WILSON, DM ;
OBRIEN, PC ;
MELTON, LJ .
NEUROLOGY, 1993, 43 (04) :817-824
[7]
GABBAY KH, 1973, NEW ENGL J MED, V288, P831, DOI 10.1056/NEJM197304192881609
[8]
The Transforming Growth Factor-β Pathway Is a Common Target of Drugs That Prevent Experimental Diabetic Retinopathy [J].
Gerhardinger, Chiara ;
Dagher, Zeina ;
Sebastiani, Paola ;
Park, Yong Seek ;
Lorenzi, Mara .
DIABETES, 2009, 58 (07) :1659-1667
[9]
Stratified analyses for selecting appropriate target patients with diabetic peripheral neuropathy for long-term treatment with an aldose reductase inhibitor, epalrestat [J].
Hotta, N. ;
Kawamori, R. ;
Atsumi, Y. ;
Baba, M. ;
Kishikawa, H. ;
Nakamura, J. ;
Oikawa, S. ;
Yamada, N. ;
Yasuda, H. ;
Shigeta, Y. .
DIABETIC MEDICINE, 2008, 25 (07) :818-825
[10]
Long-term clinical effects of epalrestat, an aldose reductase inhibitor, on diabetic peripheral neuropathy - The 3-year, multicenter, comparative aldose reductase inhibitor-diabetes complications trial [J].
Hotta, Nigishi ;
Akanuma, Yasuo ;
Kawamori, Ryuzo ;
Matsuoka, Kempe ;
Oka, Yoshitomo ;
Shichiri, Motoaki ;
Toyota, Takayoshi ;
Nakashima, Mitsuyosii ;
Yoshimura, Isao ;
Sakamoto, Nobuo ;
Shigeta, Yukio .
DIABETES CARE, 2006, 29 (07) :1538-1544