Lipid-related genetic polymorphisms significantly modulate the association between lipids and disability progression in multiple sclerosis

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Zhang, Yan
Zhou, Yuan
van der Mei, Ingrid AF
Simpson, Steve
Ponsonby, Anne-Louise
Lucas, Robyn M
Tettey, Prudence
Charlesworth, Jac
Kostner, Karam
Taylor, Bruce V
Dear, Keith
Dwyer, Terry
Blizzard, Leigh
Broadley, Simon
Kilpatrick, Trevor
Lechner-Scott, David Williamsand Jeanette
Chapman, Cameron Shawand Caron
Coulthard, Alan
Pender, Michael P
Valery, Patricia
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2019
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Abstract

Objective: To investigate whether lipid-related or body mass index (BMI)–related common genetic polymorphisms modulate the associations between serum lipid levels, BMI and disability progression in multiple sclerosis (MS).

Methods: The association between disability progression (annualised Expanded Disability Status Scale (EDSS) change over 5 years, ΔEDSS) and lipid-related or BMI-related genetic polymorphisms was evaluated in a longitudinal cohort (n=184), diagnosed with MS. We constructed a cumulative genetic risk score (CGRS) of associated polymorphisms (p<0.05) and examined the interactions between the CGRS and lipid levels (measured at baseline) in predicting ΔEDSS. All analyses were conducted using linear regression.

Results: Five lipid polymorphisms (rs2013208, rs9488822, rs17173637, rs10401969 and rs2277862) and one BMI polymorphism (rs2033529) were nominally associated with ΔEDSS. The constructed lipid CGRS showed a significant, dose-dependent association with ΔEDSS (ptrend=1.4×10−6), such that participants having ≥6 risk alleles progressed 0.38 EDSS points per year faster compared with those having ≤3. This CGRS model explained 16% of the variance in ΔEDSS. We also found significant interactions between the CGRS and lipid levels in modulating ΔEDSS, including high-density lipoprotein (HDL; pinteraction=0.005) and total cholesterol:high-density lipoprotein ratio (TC:HDL; pinteraction=0.030). The combined model (combination of CGRS and the lipid parameter) explained 26% of the disability variance for HDL and 27% for TC:HDL.

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JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

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90

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6

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© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

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Biomedical and clinical sciences

Psychology

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