Lipid profiles are associated with lesion formation over 24 months in interferon-β treated patients following the first demyelinating event
Objectives To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event. Methods High density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC...
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Published in | Journal of neurology, neurosurgery and psychiatry Vol. 84; no. 11; pp. 1186 - 1191 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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BMJ Publishing Group Ltd
01.11.2013
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Abstract | Objectives To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event. Methods High density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) were obtained in pretreatment serum from 135 high risk patients with CIS (≥2 brain MRI lesions and ≥2 oligoclonal bands) enrolled in the Observational Study of Early Interferon β-1a Treatment in High Risk Subjects after CIS study (SET study), which prospectively evaluated the effect of intramuscular interferon β-1a treatment following the first demyelinating event. Thyroid stimulating hormone, free thyroxine, 25-hydroxy vitamin D3, active smoking status and body mass index were also obtained. Clinical and MRI assessments were obtained within 4 months of the initial demyelinating event and at 6, 12 and 24 months. Results The time to first relapse and number of relapses were not associated with any of the lipid profile variables. Higher LDL-C (p=0.006) and TC (p=0.001) levels were associated with increased cumulative number of new T2 lesions over 2 years. Higher free thyroxine levels were associated with lower cumulative number of contrast-enhancing lesions (p=0.008). Higher TC was associated as a trend with lower baseline whole brain volume (p=0.020). Higher high density lipoprotein was associated with higher deseasonalised 1,25-dihydroxy vitamin D3 (p=0.003) levels and a trend was found for deseasonalised 25-hydroxy vitamin D3 (p=0.014). Conclusions In early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels are associated with inflammatory MRI activity measures. |
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AbstractList | Objectives To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event. Methods High density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) were obtained in pretreatment serum from 135 high risk patients with CIS (≥2 brain MRI lesions and ≥2 oligoclonal bands) enrolled in the Observational Study of Early Interferon β-1a Treatment in High Risk Subjects after CIS study (SET study), which prospectively evaluated the effect of intramuscular interferon β-1a treatment following the first demyelinating event. Thyroid stimulating hormone, free thyroxine, 25-hydroxy vitamin D3, active smoking status and body mass index were also obtained. Clinical and MRI assessments were obtained within 4 months of the initial demyelinating event and at 6, 12 and 24 months. Results The time to first relapse and number of relapses were not associated with any of the lipid profile variables. Higher LDL-C (p=0.006) and TC (p=0.001) levels were associated with increased cumulative number of new T2 lesions over 2 years. Higher free thyroxine levels were associated with lower cumulative number of contrast-enhancing lesions (p=0.008). Higher TC was associated as a trend with lower baseline whole brain volume (p=0.020). Higher high density lipoprotein was associated with higher deseasonalised 1,25-dihydroxy vitamin D3 (p=0.003) levels and a trend was found for deseasonalised 25-hydroxy vitamin D3 (p=0.014). Conclusions In early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels are associated with inflammatory MRI activity measures. To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event.OBJECTIVESTo investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event.High density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) were obtained in pretreatment serum from 135 high risk patients with CIS (≥ 2 brain MRI lesions and ≥ 2 oligoclonal bands) enrolled in the Observational Study of Early Interferon β-1a Treatment in High Risk Subjects after CIS study (SET study), which prospectively evaluated the effect of intramuscular interferon β-1a treatment following the first demyelinating event. Thyroid stimulating hormone, free thyroxine, 25-hydroxy vitamin D3, active smoking status and body mass index were also obtained. Clinical and MRI assessments were obtained within 4 months of the initial demyelinating event and at 6, 12 and 24 months.METHODSHigh density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) were obtained in pretreatment serum from 135 high risk patients with CIS (≥ 2 brain MRI lesions and ≥ 2 oligoclonal bands) enrolled in the Observational Study of Early Interferon β-1a Treatment in High Risk Subjects after CIS study (SET study), which prospectively evaluated the effect of intramuscular interferon β-1a treatment following the first demyelinating event. Thyroid stimulating hormone, free thyroxine, 25-hydroxy vitamin D3, active smoking status and body mass index were also obtained. Clinical and MRI assessments were obtained within 4 months of the initial demyelinating event and at 6, 12 and 24 months.The time to first relapse and number of relapses were not associated with any of the lipid profile variables. Higher LDL-C (p=0.006) and TC (p=0.001) levels were associated with increased cumulative number of new T2 lesions over 2 years. Higher free thyroxine levels were associated with lower cumulative number of contrast-enhancing lesions (p=0.008). Higher TC was associated as a trend with lower baseline whole brain volume (p=0.020). Higher high density lipoprotein was associated with higher deseasonalised 1,25-dihydroxy vitamin D3 (p=0.003) levels and a trend was found for deseasonalised 25-hydroxy vitamin D3 (p=0.014).RESULTSThe time to first relapse and number of relapses were not associated with any of the lipid profile variables. Higher LDL-C (p=0.006) and TC (p=0.001) levels were associated with increased cumulative number of new T2 lesions over 2 years. Higher free thyroxine levels were associated with lower cumulative number of contrast-enhancing lesions (p=0.008). Higher TC was associated as a trend with lower baseline whole brain volume (p=0.020). Higher high density lipoprotein was associated with higher deseasonalised 1,25-dihydroxy vitamin D3 (p=0.003) levels and a trend was found for deseasonalised 25-hydroxy vitamin D3 (p=0.014).In early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels are associated with inflammatory MRI activity measures.CONCLUSIONSIn early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels are associated with inflammatory MRI activity measures. To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating event. High density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C) and total cholesterol (TC) were obtained in pretreatment serum from 135 high risk patients with CIS (≥ 2 brain MRI lesions and ≥ 2 oligoclonal bands) enrolled in the Observational Study of Early Interferon β-1a Treatment in High Risk Subjects after CIS study (SET study), which prospectively evaluated the effect of intramuscular interferon β-1a treatment following the first demyelinating event. Thyroid stimulating hormone, free thyroxine, 25-hydroxy vitamin D3, active smoking status and body mass index were also obtained. Clinical and MRI assessments were obtained within 4 months of the initial demyelinating event and at 6, 12 and 24 months. The time to first relapse and number of relapses were not associated with any of the lipid profile variables. Higher LDL-C (p=0.006) and TC (p=0.001) levels were associated with increased cumulative number of new T2 lesions over 2 years. Higher free thyroxine levels were associated with lower cumulative number of contrast-enhancing lesions (p=0.008). Higher TC was associated as a trend with lower baseline whole brain volume (p=0.020). Higher high density lipoprotein was associated with higher deseasonalised 1,25-dihydroxy vitamin D3 (p=0.003) levels and a trend was found for deseasonalised 25-hydroxy vitamin D3 (p=0.014). In early multiple sclerosis, lipid profile variables particularly LDL-C and TC levels are associated with inflammatory MRI activity measures. |
Author | O'Connor, Kerri Seidl, Zdenek Hussein, Sara Willis, Laura Vaneckova, Manuela Badgett, Darlene Tamaño-Blanco, Miriam Ramanathan, Murali Qu, Jun Zivadinov, Robert Havrdova, Eva Lakota, Elizabeth Weinstock-Guttman, Bianca Shyh, Grace Horakova, Dana Tyblova, Michaela Krasensky, Jan Bergsland, Niels |
Author_xml | – sequence: 1 givenname: Bianca surname: Weinstock-Guttman fullname: Weinstock-Guttman, Bianca email: Murali@Buffalo.Edu organization: Department of Neurology, State University of New York, Buffalo, New York, USA – sequence: 2 givenname: Robert surname: Zivadinov fullname: Zivadinov, Robert email: Murali@Buffalo.Edu organization: Department of Neurology, Buffalo Neuroimaging Analysis Center, State University of New York, Buffalo, New York, USA – sequence: 3 givenname: Dana surname: Horakova fullname: Horakova, Dana email: Murali@Buffalo.Edu organization: Department of Neurology, Center of Clinical Neuroscience, Charles University in Prague, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 4 givenname: Eva surname: Havrdova fullname: Havrdova, Eva email: Murali@Buffalo.Edu organization: Department of Neurology, Center of Clinical Neuroscience, Charles University in Prague, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 5 givenname: Jun surname: Qu fullname: Qu, Jun email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 6 givenname: Grace surname: Shyh fullname: Shyh, Grace email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 7 givenname: Elizabeth surname: Lakota fullname: Lakota, Elizabeth email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 8 givenname: Kerri surname: O'Connor fullname: O'Connor, Kerri email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 9 givenname: Darlene surname: Badgett fullname: Badgett, Darlene email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 10 givenname: Miriam surname: Tamaño-Blanco fullname: Tamaño-Blanco, Miriam email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA – sequence: 11 givenname: Michaela surname: Tyblova fullname: Tyblova, Michaela email: Murali@Buffalo.Edu organization: Department of Neurology, Center of Clinical Neuroscience, Charles University in Prague, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 12 givenname: Sara surname: Hussein fullname: Hussein, Sara email: Murali@Buffalo.Edu organization: Department of Neurology, Buffalo Neuroimaging Analysis Center, State University of New York, Buffalo, New York, USA – sequence: 13 givenname: Niels surname: Bergsland fullname: Bergsland, Niels email: Murali@Buffalo.Edu organization: Department of Neurology, Buffalo Neuroimaging Analysis Center, State University of New York, Buffalo, New York, USA – sequence: 14 givenname: Laura surname: Willis fullname: Willis, Laura email: Murali@Buffalo.Edu organization: Department of Neurology, Buffalo Neuroimaging Analysis Center, State University of New York, Buffalo, New York, USA – sequence: 15 givenname: Jan surname: Krasensky fullname: Krasensky, Jan email: Murali@Buffalo.Edu organization: Department of Radiology, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 16 givenname: Manuela surname: Vaneckova fullname: Vaneckova, Manuela email: Murali@Buffalo.Edu organization: Department of Radiology, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 17 givenname: Zdenek surname: Seidl fullname: Seidl, Zdenek email: Murali@Buffalo.Edu organization: Department of Radiology, st Faculty of Medicine and General University Hospital, Charles University, Prague, Czech Republic – sequence: 18 givenname: Murali surname: Ramanathan fullname: Ramanathan, Murali email: Murali@Buffalo.Edu organization: Department of Pharmaceutical Sciences, State University of New York, Buffalo, New York, USA |
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Snippet | Objectives To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first... To investigate the associations of serum lipid profile with disease progression in high-risk clinically isolated syndromes (CIS) after the first demyelinating... |
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SubjectTerms | Adjuvants, Immunologic - therapeutic use Adult Body Mass Index Brain - drug effects Brain - pathology Calcifediol - blood Cholesterol - blood Cholesterol, HDL - blood Cholesterol, LDL - blood Clinical Neurology Cohort Studies Czech Republic Demyelinating Diseases - blood Demyelinating Diseases - drug therapy Early Medical Intervention Female Humans Injections, Intramuscular Interferon beta-1a Interferon-beta - therapeutic use Longitudinal Studies Magnetic Resonance Imaging Male Middle Aged Mri Multiple Sclerosis Multiple Sclerosis - blood Multiple Sclerosis - diagnosis Multiple Sclerosis - drug therapy Neurobiology Neuroradiology Prospective Studies Smoking - adverse effects Smoking - blood Thyrotropin - blood Thyroxine - blood Young Adult |
Title | Lipid profiles are associated with lesion formation over 24 months in interferon-β treated patients following the first demyelinating event |
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