Serum lipids status in patients with diabetic uremia on 10 years of maintenance hemodialysis

被引:2
作者
Sakurai, T
Akiyama, H
Oka, T
Sekita, K
Yokono, K
Goto, T
机构
[1] Kobe Univ, Sch Med, Dept Geriatr Med, Div Dialysis & Metab, Kobe, Hyogo 650, Japan
[2] Takasago Municipal Hosp, Dept Internal Med, Hyogo, Japan
关键词
APO E allele; apolipoprotein; LCAT; lipid abnormalities; long-term hemodialysis;
D O I
10.1046/j.1523-1755.1999.07156.x
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. Dyslipidemia in patients with diabetic uremic patients remains unclear. We previously reported that lipid abnormalities in diabetic uremia on short-term (3 to 28 months) hemodialysis therapy were more severe than those in nondiabetic uremic patients. The object of this study is to investigate the serum lipid profiles in diabetic uremic patients on 10 years of maintenance hemodialysis treatment. Methods. Thirty diabetic uremic subjects and 40 age-matched nondiabetic subjects on long-term hemodialysis therapy were selected, and their clinical characteristics and serum concentrations of lipids, apolipoproteins, lecithin cholesterol acyltransferase (LCAT) activity, and apolipoprotein (apo) E phenotype were evaluated, Results. Patients with diabetic uremia had a higher prevalence of macrovascular complications, including ischemic heart diseases and cerebrovascular diseases. The mean levels of serum total cholesterol, triglyceride, and high-density lipoprotein cholesterol remained normal. Nondiabetic uremic patients exhibited a reduction in serum apo A-1, serum apo A-2, serum apo C-2, and LCAT activity and an increase in serum Apo C-3, Diabetic uremic patients showed a further reduction in serum apo A-1. serum apo A-2, serum apo E, and LCAT activity. Frequencies of apo E isoforms were not significantly different between two groups of uremic patients. Conclusions. These results clearly indicate that lipid abnormalities in diabetic uremic patients on long-term hemodialysis therapy are more enhanced than those in nondiabetic uremic patients. suggesting that diabetic hemodialyzed patients an more prone to increase the individual risk for accelerated atherosclerosis to cause a higher incidence of cardiovascular diseases.
引用
收藏
页码:S216 / S218
页数:3
相关论文
共 10 条
[1]   LIPOPROTEIN METABOLISM AND RENAL-FAILURE [J].
ATTMAN, PO ;
SAMUELSSON, O ;
ALAUPOVIC, P .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 21 (06) :573-592
[2]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P599
[3]   CURRENT STATUS OF TYPE-2 (NON-INSULIN-DEPENDENT) DIABETIC SUBJECTS ON DIALYSIS THERAPY IN JAPAN [J].
KIKKAWA, R ;
ARIMURA, T ;
HANEDA, M ;
NISHIO, T ;
SAWADA, K ;
YAGISAWA, M ;
SHIGETA, Y .
DIABETOLOGIA, 1993, 36 (10) :1105-1108
[4]   APOLIPOPROTEIN-E - CHOLESTEROL TRANSPORT PROTEIN WITH EXPANDING ROLE IN CELL BIOLOGY [J].
MAHLEY, RW .
SCIENCE, 1988, 240 (4852) :622-630
[5]   APOLIPOPROTEIN-E PHENOTYPING FROM SERUM BY WESTERN BLOTTING [J].
MENZEL, HJ ;
UTERMANN, G .
ELECTROPHORESIS, 1986, 7 (11) :492-495
[6]   ABNORMAL LIPOPROTEIN METABOLISM IN NON-INSULIN-DEPENDENT DIABETES-MELLITUS - PATHOGENESIS AND TREATMENT [J].
REAVEN, GM .
AMERICAN JOURNAL OF MEDICINE, 1987, 83 (3A) :31-39
[7]   COMPARISON OF LIPIDS, APOPROTEINS AND ASSOCIATED ENZYME-ACTIVITIES BETWEEN DIABETIC AND NONDIABETIC END-STAGE RENAL-DISEASE [J].
SAKURAI, T ;
OKA, T ;
HASEGAWA, H ;
IGAKI, N ;
MIKI, S ;
GOTO, T .
NEPHRON, 1992, 61 (04) :409-414
[8]  
Uustitupa Mij, 1990, CIRCULATION, V82, P27
[9]   HYPERLIPOPROTEINEMIA IN CHRONIC-RENAL-FAILURE - PATHOPHYSIOLOGICAL AND THERAPEUTIC ASPECTS [J].
WANNER, C ;
FROMMHERZ, K ;
HORL, WH .
CARDIOLOGY, 1991, 78 (03) :202-217
[10]   DOSE-DEPENDENT ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET, SPORADIC ALZHEIMERS-DISEASE [J].
YOSHIZAWA, T ;
YAMAKAWAKOBAYASHI, K ;
KOMATSUZAKI, Y ;
ARINAMI, T ;
OGUNI, E ;
MIZUSAWA, H ;
SHOJI, S ;
HAMAGUCHI, H .
ANNALS OF NEUROLOGY, 1994, 36 (04) :656-659