Paraoxonase 1 activity: A new vascular marker of dementia

被引:47
作者
Dantoine, TF
Debord, J
Merle, L
Lacroix-Raminandrisoa, H
Bourzeix, L
Charmes, JP
机构
[1] Ctr Hosp Univ, Dept Gerontol Clin, F-87042 Limoges, France
[2] Fac Med, Pharmacol Lab, F-87000 Limoges, France
来源
ALZHEIMER'S DISEASE: VASCULAR ETIOLOGY AND PATHOLOGY | 2002年 / 977卷
关键词
Alzheimer's disease; vascular dementia; cognitive disorder; paraoxonase 1 (PON1) activity;
D O I
10.1111/j.1749-6632.2002.tb04802.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Paraoxonase 1 (PON1), an A-esterase with peroxidase-like activity present on the surface of HDL, decreases the peroxidation of LDL. Serum PON1 activity (PON1a) decreases with aging and in disorders associated with a high risk of adverse cardiovascular events (acute myocardial infarction, diabetes mellitus, and chronic renal failure). The implication of vascular factors in Alzheimer-type dementia (ATD) is strongly suspected. We measured PON1a by spectrophotometry using the paraoxon substrate in 180 healthy subjects (controls; mean age: 75.3 +/- 8.9 years; 98 women) and 154 patients admitted for cognitive testing. According to criteria, 45 patients had mild cognitive impairments (MCI; mean age: 75.6 +/- 9.3 years; 28 women), 60 had ATD (mean age: 75.6 +/- 8.3 years; 47 women), and 49 had vascular dementia (VaD; mean age: 77.5 +/- 7.2 years; 33 women). Mean PON1a was lower in VaD (0.25 +/- 0.1 U/mL) than in controls or ATD (both 0.41 +/- 0.2 U/mL,p < 0.01). Mean PON1a values in MCI (0.34 +/- 0.2 U/mL) and ATD (0.41 +/- 0.2 U/mL) were not significantly different. In multiple linear regression, PON1a was negatively correlated with male sex, age, and VaD, and positively correlated with ATD (each correlation p < 0.001). As shown in other high-risk cardiovascular disorders, PON1a seems to be a reliable marker of VaD. Its modification in Alzheimer's disease supports the implication of vascular risk factors in this type of dementia.
引用
收藏
页码:96 / 101
页数:6
相关论文
共 24 条
[1]   Dementia is the major cause of functional dependence in the elderly:: 3-year follow-up data from a population-based study [J].
Agüero-Torres, H ;
Fratiglioni, L ;
Guo, ZC ;
Viitanen, M ;
von Strauss, E ;
Winblad, B .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1998, 88 (10) :1452-1456
[2]   Human serum paraoxonases (PON1) Q and R selectively decrease lipid peroxides in human coronary and carotid atherosclerotic lesions - PON1 esterase and peroxidase-like activities [J].
Aviram, M ;
Hardak, E ;
Vaya, J ;
Mahmood, S ;
Milo, S ;
Hoffman, A ;
Billicke, S ;
Draganov, D ;
Rosenblat, M .
CIRCULATION, 2000, 101 (21) :2510-2517
[3]   Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions - A possible peroxidative role for paraoxonase [J].
Aviram, M ;
Rosenblat, M ;
Bisgaier, CL ;
Newton, RS ;
Primo-Parmo, SL ;
La Du, BN .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (08) :1581-1590
[4]   IDENTIFICATION OF A DISTINCT HUMAN HIGH-DENSITY-LIPOPROTEIN SUBSPECIES DEFINED BY A LIPOPROTEIN-ASSOCIATED PROTEIN, K-45 - IDENTITY OF K-45 WITH PARAOXONASE [J].
BLATTER, MC ;
JAMES, RW ;
MESSMER, S ;
BARJA, F ;
POMETTA, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 211 (03) :871-879
[5]   REVERSAL OF AGE-RELATED INCREASE IN BRAIN PROTEIN OXIDATION, DECREASE IN ENZYME-ACTIVITY, AND LOSS IN TEMPORAL AND SPATIAL MEMORY BY CHRONIC ADMINISTRATION OF THE SPIN-TRAPPING COMPOUND N-TERT-BUTYL-ALPHA-PHENYLNITRONE [J].
CARNEY, JM ;
STARKEREED, PE ;
OLIVER, CN ;
LANDUM, RW ;
CHENG, MS ;
WU, JF ;
FLOYD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3633-3636
[6]   OXIDATIVE STRESS AND ALZHEIMERS-DISEASE [J].
CHOI, BH .
NEUROBIOLOGY OF AGING, 1995, 16 (04) :675-678
[7]  
Dantoine TF, 1998, J AM SOC NEPHROL, V9, P2082
[8]   Worldwide prevalence and incidence of dementia [J].
Fratiglioni, L ;
De Ronchi, D ;
Agüero-Torres, H .
DRUGS & AGING, 1999, 15 (05) :365-375
[9]   BETA-AMYLOID PEPTIDE-DERIVED, OXYGEN-DEPENDENT FREE-RADICALS INHIBIT GLUTAMATE UPTAKE IN CULTURED ASTROCYTES - IMPLICATIONS FOR ALZHEIMERS-DISEASE [J].
HARRIS, ME ;
CARNEY, JM ;
COLE, PS ;
HENSLEY, K ;
HOWARD, BJ ;
MARTIN, L ;
BUMMER, P ;
WANG, YN ;
PEDIGO, NW ;
BUTTERFIELD, DA .
NEUROREPORT, 1995, 6 (14) :1875-1879
[10]   A MODEL FOR BETA-AMYLOID AGGREGATION AND NEUROTOXICITY BASED ON FREE-RADICAL GENERATION BY THE PEPTIDE - RELEVANCE TO ALZHEIMER-DISEASE [J].
HENSLEY, K ;
CARNEY, JM ;
MATTSON, MP ;
AKSENOVA, M ;
HARRIS, M ;
WU, JF ;
FLOYD, RA ;
BUTTERFIELD, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (08) :3270-3274