ECTRIMS eLearning

An adverse lipid profile and increased body mass index significantly predicts clinical course after a first demyelinating event
Author(s): ,
I van der Mei
Affiliations:
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS
,
P Tettey
Affiliations:
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS
,
S Simpson Jr.
Affiliations:
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS
,
B Taylor
Affiliations:
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS
,
R Lucas
Affiliations:
National Centre for Epidemiology and Population Health, Australian National University, Canberra, ACT
A.-L Ponsonby
Affiliations:
Murdoch Childrens Research Institute, Melbourne, VIC, Australia
ECTRIMS Learn. van der Mei I. 09/15/16; 146158; P317
Ingrid van der Mei
Ingrid van der Mei
Contributions
Abstract

Abstract: P317

Type: Poster

Abstract Category: Clinical aspects of MS - Epidemiology

Background: Data on whether the accumulation of disability and relapse may be influenced by serum lipid levels and body mass index (BMI) in patients with a first clinical diagnosis of demyelination is limited. We aimed to investigate whether there were any associations between lipid-related variables at cohort entry and conversion to clinically definite MS (CDMS), time to subsequent relapse and progression in disability.

Methods: A cohort of 279 patients with a first clinical diagnosis of demyelination from the Ausimmune Study was prospectively followed up to 5-year review. Height and weight were measured and serum samples taken at baseline to measure lipid profile and apolipoprotein levels. Associations with conversion to CDMS and hazard of relapse were assessed using survival analysis and associations with annual change in disability were evaluated using linear regression.

Results: Higher body mass index (BMI) (Adjusted hazard ratio (AHR) 1.04 (95% CI 1.01, 1.08) p=0.014) and triglyceride levels (AHR 1.20 (95% CI 1.03, 1.40) p=0.021) at cohort entry were associated with increased risk of subsequent relapse while lipid-related measures were not significantly associated with conversion to CDMS. In addition, higher BMI (β 0.01 (95% CI 0.001, 0.13) p=0.010) and the ratio of total cholesterol over high density lipoprotein (TC/HDL ratio) (β 0.05 (95% CI 0.001, 0.10) p=0.044) at cohort entry were associated with a higher subsequent annual change in disability.

Conclusions: In this prospective study, we have demonstrated that higher BMI and triglycerides at first clinical diagnosis of CNS demyelination were associated with increased hazard of relapse, and a higher BMI and TC/HDL ratio were associated with a higher rate in disability progression. Improving lipid profile and losing weight into the healthy range may improve the disease course of MS.

Disclosure: Authors have no relevant disclosures.

Abstract: P317

Type: Poster

Abstract Category: Clinical aspects of MS - Epidemiology

Background: Data on whether the accumulation of disability and relapse may be influenced by serum lipid levels and body mass index (BMI) in patients with a first clinical diagnosis of demyelination is limited. We aimed to investigate whether there were any associations between lipid-related variables at cohort entry and conversion to clinically definite MS (CDMS), time to subsequent relapse and progression in disability.

Methods: A cohort of 279 patients with a first clinical diagnosis of demyelination from the Ausimmune Study was prospectively followed up to 5-year review. Height and weight were measured and serum samples taken at baseline to measure lipid profile and apolipoprotein levels. Associations with conversion to CDMS and hazard of relapse were assessed using survival analysis and associations with annual change in disability were evaluated using linear regression.

Results: Higher body mass index (BMI) (Adjusted hazard ratio (AHR) 1.04 (95% CI 1.01, 1.08) p=0.014) and triglyceride levels (AHR 1.20 (95% CI 1.03, 1.40) p=0.021) at cohort entry were associated with increased risk of subsequent relapse while lipid-related measures were not significantly associated with conversion to CDMS. In addition, higher BMI (β 0.01 (95% CI 0.001, 0.13) p=0.010) and the ratio of total cholesterol over high density lipoprotein (TC/HDL ratio) (β 0.05 (95% CI 0.001, 0.10) p=0.044) at cohort entry were associated with a higher subsequent annual change in disability.

Conclusions: In this prospective study, we have demonstrated that higher BMI and triglycerides at first clinical diagnosis of CNS demyelination were associated with increased hazard of relapse, and a higher BMI and TC/HDL ratio were associated with a higher rate in disability progression. Improving lipid profile and losing weight into the healthy range may improve the disease course of MS.

Disclosure: Authors have no relevant disclosures.

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