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Interleukin-6 gene promoter-572 C allele may play a role in rate of disease progression in multiple sclerosis

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posted on 2025-05-11, 11:38 authored by Jun Yan, Jia Liu, Deborah Mason, Lyn Griffiths, Pablo MoscatoPablo Moscato, Mark Slee, Bruce Taylor, James Wiley, Judith Field, Helmut Butzkueven, Trevor J. Kilpatrick, Peter A. Csurhes, Clement Yihao Lin, Michael P. Pender, Pamela A. McCombe, Judith M. Greer, Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZGene), Rodney ScottRodney Scott, Jeannette Lechner-ScottJeannette Lechner-Scott, Matthew A. Brown, David R. Booth, Graeme J. Stewart, Simon Broadley
Multiple sclerosis (MS) is an inflammatory demyelinating disease affecting the central nervous system. Although the exact pathogenesis of MS is unknown, it is generally considered to be an autoimmune disease, with numerous genetic and environmental factors determining disease susceptibility and severity. One important mediator of immune responses and inflammation is interleukin-6 (IL-6). Previously, elevated levels of IL-6 in mononuclear cells in blood and in brain tissue from MS patients have been reported. Various polymorphisms in the promoter region of the IL6 gene have also been linked with IL-6 protein levels. In MS, several small studies have investigated whether two IL6 promoter polymorphisms (−597 G>A and −174 G>C) correlate with MS susceptibility, but with varying results. In the present study, we analyzed these polymorphisms, together with an additional polymorphism (−572 G>C) in 279 healthy controls and 509 patients with MS. We found no significant differences between MS patients and healthy controls for the different −597 or −174 IL6 promoter alleles or genotypes. There was a slight reduction in the percentage of individuals with MS who carried a C allele at position −572, although this was not significant after correction for multiple comparisons. Interestingly, however, the −572 C allele showed a significant correlation with the MS severity score, suggesting a possible role in disease progression.

History

Journal title

International Journal of Molecular Sciences

Volume

13

Issue

10

Pagination

13667-13679

Publisher

MDPIAG

Language

  • en, English

College/Research Centre

Faculty of Engineering and Built Environment

School

School of Electrical Engineering and Computer Science

Rights statement

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0)

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