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Apolipoproteins are associated with new MRI lesions and deep grey matter atrophy in clinically isolated syndromes
RW. Browne, B. Weinstock-Guttman, D. Horakova, R. Zivadinov, ML. Bodziak, M. Tamaño-Blanco, D. Badgett, M. Tyblova, M. Vaneckova, Z. Seidl, J. Krasensky, N. Bergsland, DP. Ramasamy, J. Hagemeier, E. Havrdova, M. Ramanathan,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, multicentrická studie, pozorovací studie, Research Support, U.S. Gov't, Non-P.H.S.
Grantová podpora
NT13237
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
ProQuest Central
od 1944-07-01 do Před 6 měsíci
Nursing & Allied Health Database (ProQuest)
od 1944-07-01 do Před 6 měsíci
Health & Medicine (ProQuest)
od 1944-07-01 do Před 6 měsíci
Psychology Database (ProQuest)
od 1944-07-01 do Před 6 měsíci
PubMed
24470599
DOI
10.1136/jnnp-2013-307106
Knihovny.cz E-zdroje
- MeSH
- antiflogistika terapeutické užití MeSH
- apolipoproteiny E krev MeSH
- apolipoproteiny metabolismus MeSH
- atrofie MeSH
- dospělí MeSH
- interpretace statistických dat MeSH
- lidé středního věku MeSH
- lidé MeSH
- lipidy krev MeSH
- longitudinální studie MeSH
- magnetická rezonanční tomografie MeSH
- methylprednisolon terapeutické užití MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mozek patologie MeSH
- počítačové zpracování obrazu MeSH
- progrese nemoci MeSH
- prospektivní studie MeSH
- roztroušená skleróza metabolismus patologie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
OBJECTIVES: There is increasing evidence that serum lipoprotein cholesterol biomarkers are associated with disease progression in clinically isolated syndromes (CIS). Apolipoproteins (Apo) are recognition ligands that mediate the physiological interactions of cholesterol-containing lipoproteins. The objective of this study was to investigate whether serum Apo levels are associated with CIS disease progression. METHODS: ApoB, ApoAI, ApoAII, ApoE and lipoprotein (a) (Lpa) levels were measured in serum samples obtained prior to the start of treatment from 181 CIS patients (123 women, 58 men, 68% women; mean age: 28.1±SD 8.1 years). All patients were treated with intramuscular interferon-β as part of the prospective study. Clinical and MRI assessments were obtained at baseline, 6, 12 and 24 months after start of interferon-β treatment. RESULTS: Greater ApoB levels were associated with increased number of new T2 lesions (p<0.001) and increased number of new or enlarging T2 lesions (p<0.001) over 2 years. Each 10 mg/dL of greater baseline ApoB is associated with a 16% increase in the number of new T2 lesions over 2 years. ApoAI, ApoAII, ApoE and Lpa were not associated with T2 lesions. Greater ApoE levels were associated with greater deep grey matter atrophy (partial correlation rp=-0.28, p<0.001). Each 1 mg/dL increment in ApoE levels was associated with a 1% increase in deep grey matter atrophy over 2 years. CONCLUSIONS: Serum ApoB levels are associated with new lesion accumulation whereas ApoE levels are associated with deep grey matter atrophy in high risk CIS patients treated with interferon β-1a.
Department of Neurology State University of New York Buffalo New York USA
Department of Pharmaceutical Sciences State University of New York Buffalo New York USA
Citace poskytuje Crossref.org
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