Atherogenic lipoprotein phenotype in end-stage renal failure: Origin and extent of small dense low-density lipoprotein formation

被引:110
作者
Deighan, CJ
Caslake, MJ
McConnell, M
Boulton-Jones, JM
Packard, CJ
机构
[1] Univ Glasgow, Glasgow Royal Infirm, NHS Trust, Renal Unit, Glasgow G4 0SF, Lanark, Scotland
[2] Univ Glasgow, Glasgow Royal Infirm, NHS Trust, Dept Pathol Biochem, Glasgow G4 0SF, Lanark, Scotland
关键词
end-stage renal failure (ESRF); lipoproteins; low density lipoprotein (LDL) subfractions; small dense low-density lipoprotein (LDLIII); cardiovascular risk;
D O I
10.1016/S0272-6386(00)70255-1
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 [临床医学]; 100201 [内科学];
摘要
End-stage renal failure (ESRF) is associated with dyslipidemia and accelerated atherosclerosis. Triglyceride-rich lipoproteins accumulate and qualitative changes take place in low-density lipoprotein (LDL), with a predominance of the small dense LDL phenotype. Increased small dense LDL (LDLIII) is a known risk factor for cardiovascular disease. To assess the extent of LDLIII formation in ESRF and identify factors contributing to LDLIII production, we analyzed LDL subfractions by density-gradient ultracentrifugation, very low-density lipoprotein subfractions, and lipase activity in 75 patients with ESRF (25 hemodialysis [HD], 25 peritoneal dialysis [PD], and 25 predialysis patients) and 40 age- and sex-matched controls. The percentage of LDLIII was increased in all three patient groups compared with controls (PD, 33% +/- 29% [mean +/- SD]; P < 0.005; HD, 30% +/- 22%; P < 0.01; predialysis, 26% +/- 26%; P < 0.01;all versus controls, 14% +/- 10%). Plasma LDLIII concentration was increased only in PD patients (median, 84 mg/dL; interquartile range [IQR], 29 to 160 mg/dL versus controls; median, 31 mg/dL; IQR, 26 to 54 mg/dL). In other patient groups, total LDL level was less, with heterogeneity in LDLIII concentrations. Forty percent of PD patients and 28% of HD and predialysis patients had LDLIII concentrations greater than 100 mg/dL compared with 2.5% of controls (P = 0.002). Plasma triglyceride levels (r(2) = 38.4%; P < 0.001) and hepatic lipase activity (r(2) = 6.7%; P < 0.03) were Independent predictors of LDLIII concentration. The strong association between LDLIII concentration and triglyceride level was present in all three patient groups (HD, r(2) = 47.9%; PD, r(2) = 45.2%; predialysis, r(2) = 25.8%); plasma triglyceride levels greater than 177 mg/dL (2.0 mmol/L) had an 86% specificity and 79% sensitivity for predicting an LDLIII concentration greater than 100 mg/dL. We conclude that the atherogenic lipoprotein phenotype predominates in ESRF, with excess LDLIII particularly prominent in PD patients. Atherogenic levels of LDLIII are found in patients with triglyceride levels greater than 177 mg/dL. This is likely to represent a further cardiovascular risk factor in this population. (C) 2000 by the National Kidney Foundation, Inc.
引用
收藏
页码:852 / 862
页数:11
相关论文
共 34 条
[1]
Influence of plasma lipid and LDL-subfraction profile on the interaction between low density lipoprotein with human arterial wall proteoglycans [J].
Anber, V ;
Griffin, BA ;
McConnell, M ;
Packard, CJ ;
Shepherd, J .
ATHEROSCLEROSIS, 1996, 124 (02) :261-271
[2]
EVIDENCE THAT REDUCED LIPOPROTEIN-LIPASE ACTIVITY IS NOT A PRIMARY PATHOGENETIC FACTOR FOR HYPERTRIGLYCERIDEMIA IN RENAL-FAILURE [J].
ARNADOTTIR, M ;
THYSELL, H ;
DALLONGEVILLE, J ;
FRUCHART, JC ;
NILSSONEHLE, P .
KIDNEY INTERNATIONAL, 1995, 48 (03) :779-784
[3]
Increased activity of plasma cholesteryl ester transfer protein in children with end-stage renal disease receiving continuous ambulatory peritoneal dialysis [J].
Asayama, K ;
Hayashibe, H ;
Mishiku, Y ;
Honda, M ;
Ito, H ;
Nakazawa, S .
NEPHRON, 1996, 72 (02) :231-236
[4]
LIPOPROTEIN METABOLISM AND RENAL-FAILURE [J].
ATTMAN, PO ;
SAMUELSSON, O ;
ALAUPOVIC, P .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 21 (06) :573-592
[5]
ATHEROGENIC LIPOPROTEIN PHENOTYPE - A PROPOSED GENETIC-MARKER FOR CORONARY HEART-DISEASE RISK [J].
AUSTIN, MA ;
KING, MC ;
VRANIZAN, KM ;
KRAUSS, RM .
CIRCULATION, 1990, 82 (02) :495-506
[6]
ENHANCED SUSCEPTIBILITY TO INVITRO OXIDATION OF THE DENSE LOW-DENSITY-LIPOPROTEIN SUBFRACTION IN HEALTHY-SUBJECTS [J].
DEGRAAF, J ;
HAKLEMMERS, HLM ;
HECTORS, MPC ;
DEMACKER, PNM ;
HENDRIKS, JCM ;
STALENHOEF, AFH .
ARTERIOSCLEROSIS AND THROMBOSIS, 1991, 11 (02) :298-306
[7]
PLASMA-CHOLESTEROL METABOLISM IN END-STAGE RENAL-DISEASE - DIFFERENCE BETWEEN TREATMENT BY HEMODIALYSIS OR PERITONEAL-DIALYSIS [J].
DIEPLINGER, H ;
SCHOENFELD, PY ;
FIELDING, CJ .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (04) :1071-1083
[8]
Clinical epidemiology of cardiovascular disease in chronic renal disease [J].
Foley, RN ;
Parfrey, PS ;
Sarnak, MJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (05) :S112-S119
[9]
Association of small low-density lipoprotein particles with the incidence of coronary artery disease in men and women [J].
Gardner, CD ;
Fortmann, SP ;
Krauss, RM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (11) :875-881
[10]
RAPID ISOLATION OF LOW-DENSITY-LIPOPROTEIN (LDL) SUBFRACTIONS FROM PLASMA BY DENSITY GRADIENT ULTRACENTRIFUGATION [J].
GRIFFIN, BA ;
CASLAKE, MJ ;
YIP, B ;
TAIT, GW ;
PACKARD, CJ ;
SHEPHERD, J .
ATHEROSCLEROSIS, 1990, 83 (01) :59-67