Movement Disorders (revue)

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Serum Cholesterol Levels and the Risk of Multiple System Atrophy : A Case-Control Study

Identifieur interne : 000F14 ( PascalFrancis/Corpus ); précédent : 000F13; suivant : 000F15

Serum Cholesterol Levels and the Risk of Multiple System Atrophy : A Case-Control Study

Auteurs : PHIL HYU LEE ; TAE SUNG LIM ; Hae-Won Shin ; SEOK WOO YONG ; HYO SUK NAM ; Young H. Sohn

Source :

RBID : Pascal:09-0218148

Descripteurs français

English descriptors

Abstract

Cholesterol in brain membranes may modulate the conformational state and accumulation of α-synuclein in α-synucleinopathies. We examined the association between serum cholesterol and the risk of multiple system atrophy (MSA), one of the α-synucleinopathies. We enrolled 142 patients with probable MSA from two tertiary referral hospitals and 155 age- and gender-matched healthy people with no neurological disease. The levels of total cholesterol, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were significantly lower in MSA patients than in controls (total cholesterol: 172.7 vs. 196.3 mg/dL, P < 0.001; LDL-C: 104.0 vs. 115.3 mg/dL, P = 0.001; HDL-C: 47.3 vs. 54.2 mg/dL, P < 0.001). After adjusting for age, gender, use of cholesterol-lowering drugs, and histories of hypertension, diabetes mellitus, and smoking, the odds ratios was 5.9 (95% CI = 2.3-11.5, P < 0.001) for MSA patients in the lowest quartile of total cholesterol and 2.6 (95% CI = 1.2-5.5, P = 0.016) for those in the lowest quartile of HDL-C, compared with the highest quartiles. Levels of serum cholesterol did not significantly correlate with disease duration or severity. Our data suggest that lower levels of total cholesterol and HDL may be associated with an increased risk of MSA.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
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A03   1    @0 Mov. disord.
A05       @2 24
A06       @2 5
A08 01  1  ENG  @1 Serum Cholesterol Levels and the Risk of Multiple System Atrophy : A Case-Control Study
A11 01  1    @1 PHIL HYU LEE
A11 02  1    @1 TAE SUNG LIM
A11 03  1    @1 SHIN (Hae-Won)
A11 04  1    @1 SEOK WOO YONG
A11 05  1    @1 HYO SUK NAM
A11 06  1    @1 SOHN (Young H.)
A14 01      @1 Department of Neurology, Yonsei University College of Medicine @2 Seoul @3 KOR @Z 1 aut. @Z 5 aut. @Z 6 aut.
A14 02      @1 Department of Neurology, Ajou University School of Medicine @2 Suwon @3 KOR @Z 2 aut. @Z 4 aut.
A14 03      @1 Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine @2 Seoul @3 KOR @Z 3 aut.
A20       @1 752-758
A21       @1 2009
A23 01      @0 ENG
A43 01      @1 INIST @2 20953 @5 354000186090170180
A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
A45       @0 37 ref.
A47 01  1    @0 09-0218148
A60       @1 P
A61       @0 A
A64 01  1    @0 Movement disorders
A66 01      @0 USA
C01 01    ENG  @0 Cholesterol in brain membranes may modulate the conformational state and accumulation of α-synuclein in α-synucleinopathies. We examined the association between serum cholesterol and the risk of multiple system atrophy (MSA), one of the α-synucleinopathies. We enrolled 142 patients with probable MSA from two tertiary referral hospitals and 155 age- and gender-matched healthy people with no neurological disease. The levels of total cholesterol, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were significantly lower in MSA patients than in controls (total cholesterol: 172.7 vs. 196.3 mg/dL, P < 0.001; LDL-C: 104.0 vs. 115.3 mg/dL, P = 0.001; HDL-C: 47.3 vs. 54.2 mg/dL, P < 0.001). After adjusting for age, gender, use of cholesterol-lowering drugs, and histories of hypertension, diabetes mellitus, and smoking, the odds ratios was 5.9 (95% CI = 2.3-11.5, P < 0.001) for MSA patients in the lowest quartile of total cholesterol and 2.6 (95% CI = 1.2-5.5, P = 0.016) for those in the lowest quartile of HDL-C, compared with the highest quartiles. Levels of serum cholesterol did not significantly correlate with disease duration or severity. Our data suggest that lower levels of total cholesterol and HDL may be associated with an increased risk of MSA.
C02 01  X    @0 002B17
C02 02  X    @0 002B17F
C03 01  X  FRE  @0 Atrophie multisystématisée @2 NM @5 01
C03 01  X  ENG  @0 Multiple system atrophy @2 NM @5 01
C03 01  X  SPA  @0 Atrofia multisistematizada @2 NM @5 01
C03 02  X  FRE  @0 Pathologie du système nerveux @5 02
C03 02  X  ENG  @0 Nervous system diseases @5 02
C03 02  X  SPA  @0 Sistema nervioso patología @5 02
C03 03  X  FRE  @0 Cholestérol @2 NK @5 09
C03 03  X  ENG  @0 Cholesterol @2 NK @5 09
C03 03  X  SPA  @0 Colesterol @2 NK @5 09
C03 04  X  FRE  @0 Facteur risque @5 10
C03 04  X  ENG  @0 Risk factor @5 10
C03 04  X  SPA  @0 Factor riesgo @5 10
C03 05  X  FRE  @0 Etude cas témoin @5 11
C03 05  X  ENG  @0 Case control study @5 11
C03 05  X  SPA  @0 Estudio caso control @5 11
C07 01  X  FRE  @0 Lipide @5 37
C07 01  X  ENG  @0 Lipids @5 37
C07 01  X  SPA  @0 Lípido @5 37
N21       @1 159
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 09-0218148 INIST
ET : Serum Cholesterol Levels and the Risk of Multiple System Atrophy : A Case-Control Study
AU : PHIL HYU LEE; TAE SUNG LIM; SHIN (Hae-Won); SEOK WOO YONG; HYO SUK NAM; SOHN (Young H.)
AF : Department of Neurology, Yonsei University College of Medicine/Seoul/Corée, République de (1 aut., 5 aut., 6 aut.); Department of Neurology, Ajou University School of Medicine/Suwon/Corée, République de (2 aut., 4 aut.); Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine/Seoul/Corée, République de (3 aut.)
DT : Publication en série; Niveau analytique
SO : Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2009; Vol. 24; No. 5; Pp. 752-758; Bibl. 37 ref.
LA : Anglais
EA : Cholesterol in brain membranes may modulate the conformational state and accumulation of α-synuclein in α-synucleinopathies. We examined the association between serum cholesterol and the risk of multiple system atrophy (MSA), one of the α-synucleinopathies. We enrolled 142 patients with probable MSA from two tertiary referral hospitals and 155 age- and gender-matched healthy people with no neurological disease. The levels of total cholesterol, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were significantly lower in MSA patients than in controls (total cholesterol: 172.7 vs. 196.3 mg/dL, P < 0.001; LDL-C: 104.0 vs. 115.3 mg/dL, P = 0.001; HDL-C: 47.3 vs. 54.2 mg/dL, P < 0.001). After adjusting for age, gender, use of cholesterol-lowering drugs, and histories of hypertension, diabetes mellitus, and smoking, the odds ratios was 5.9 (95% CI = 2.3-11.5, P < 0.001) for MSA patients in the lowest quartile of total cholesterol and 2.6 (95% CI = 1.2-5.5, P = 0.016) for those in the lowest quartile of HDL-C, compared with the highest quartiles. Levels of serum cholesterol did not significantly correlate with disease duration or severity. Our data suggest that lower levels of total cholesterol and HDL may be associated with an increased risk of MSA.
CC : 002B17; 002B17F
FD : Atrophie multisystématisée; Pathologie du système nerveux; Cholestérol; Facteur risque; Etude cas témoin
FG : Lipide
ED : Multiple system atrophy; Nervous system diseases; Cholesterol; Risk factor; Case control study
EG : Lipids
SD : Atrofia multisistematizada; Sistema nervioso patología; Colesterol; Factor riesgo; Estudio caso control
LO : INIST-20953.354000186090170180
ID : 09-0218148

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Pascal:09-0218148

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<div type="abstract" xml:lang="en">Cholesterol in brain membranes may modulate the conformational state and accumulation of α-synuclein in α-synucleinopathies. We examined the association between serum cholesterol and the risk of multiple system atrophy (MSA), one of the α-synucleinopathies. We enrolled 142 patients with probable MSA from two tertiary referral hospitals and 155 age- and gender-matched healthy people with no neurological disease. The levels of total cholesterol, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were significantly lower in MSA patients than in controls (total cholesterol: 172.7 vs. 196.3 mg/dL, P < 0.001; LDL-C: 104.0 vs. 115.3 mg/dL, P = 0.001; HDL-C: 47.3 vs. 54.2 mg/dL, P < 0.001). After adjusting for age, gender, use of cholesterol-lowering drugs, and histories of hypertension, diabetes mellitus, and smoking, the odds ratios was 5.9 (95% CI = 2.3-11.5, P < 0.001) for MSA patients in the lowest quartile of total cholesterol and 2.6 (95% CI = 1.2-5.5, P = 0.016) for those in the lowest quartile of HDL-C, compared with the highest quartiles. Levels of serum cholesterol did not significantly correlate with disease duration or severity. Our data suggest that lower levels of total cholesterol and HDL may be associated with an increased risk of MSA.</div>
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<NO>PASCAL 09-0218148 INIST</NO>
<ET>Serum Cholesterol Levels and the Risk of Multiple System Atrophy : A Case-Control Study</ET>
<AU>PHIL HYU LEE; TAE SUNG LIM; SHIN (Hae-Won); SEOK WOO YONG; HYO SUK NAM; SOHN (Young H.)</AU>
<AF>Department of Neurology, Yonsei University College of Medicine/Seoul/Corée, République de (1 aut., 5 aut., 6 aut.); Department of Neurology, Ajou University School of Medicine/Suwon/Corée, République de (2 aut., 4 aut.); Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine/Seoul/Corée, République de (3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2009; Vol. 24; No. 5; Pp. 752-758; Bibl. 37 ref.</SO>
<LA>Anglais</LA>
<EA>Cholesterol in brain membranes may modulate the conformational state and accumulation of α-synuclein in α-synucleinopathies. We examined the association between serum cholesterol and the risk of multiple system atrophy (MSA), one of the α-synucleinopathies. We enrolled 142 patients with probable MSA from two tertiary referral hospitals and 155 age- and gender-matched healthy people with no neurological disease. The levels of total cholesterol, low-density lipoprotein cholesterol (LDL-C), and high-density lipoprotein cholesterol (HDL-C) were significantly lower in MSA patients than in controls (total cholesterol: 172.7 vs. 196.3 mg/dL, P < 0.001; LDL-C: 104.0 vs. 115.3 mg/dL, P = 0.001; HDL-C: 47.3 vs. 54.2 mg/dL, P < 0.001). After adjusting for age, gender, use of cholesterol-lowering drugs, and histories of hypertension, diabetes mellitus, and smoking, the odds ratios was 5.9 (95% CI = 2.3-11.5, P < 0.001) for MSA patients in the lowest quartile of total cholesterol and 2.6 (95% CI = 1.2-5.5, P = 0.016) for those in the lowest quartile of HDL-C, compared with the highest quartiles. Levels of serum cholesterol did not significantly correlate with disease duration or severity. Our data suggest that lower levels of total cholesterol and HDL may be associated with an increased risk of MSA.</EA>
<CC>002B17; 002B17F</CC>
<FD>Atrophie multisystématisée; Pathologie du système nerveux; Cholestérol; Facteur risque; Etude cas témoin</FD>
<FG>Lipide</FG>
<ED>Multiple system atrophy; Nervous system diseases; Cholesterol; Risk factor; Case control study</ED>
<EG>Lipids</EG>
<SD>Atrofia multisistematizada; Sistema nervioso patología; Colesterol; Factor riesgo; Estudio caso control</SD>
<LO>INIST-20953.354000186090170180</LO>
<ID>09-0218148</ID>
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