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ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK.

Jacobs, BM; Schalk, L; Dunne, A; Scalfari, A; Nandoskar, A; Gran, B; Mein, CA; Sellers, C; Spilker, C; Rog, D; et al. Jacobs, BM; Schalk, L; Dunne, A; Scalfari, A; Nandoskar, A; Gran, B; Mein, CA; Sellers, C; Spilker, C; Rog, D; Visentin, E; Bezzina, EL; Uzochukwu, E; Tallantyre, E; Wozniak, E; Sacre, E; Hassan-Smith, G; Ford, HL; Harris, J; Bradley, J; Breedon, J; Brooke, J; Kreft, KL; Tuite Dalton, K; George, K; Papachatzaki, M; O'Malley, M; Peter, M; Mattoscio, M; Rhule, N; Evangelou, N; Vinod, N; Quinn, O; Shamji, R; Kaimal, R; Boulton, R; Tanveer, R; Middleton, R; Murray, R; Bellfield, R; Hoque, S; Patel, S; Raj, S; Gumus, S; Mitchell, S; Sawcer, S; Arun, T; Pogreban, T; Brown, T-L; Begum, T; Antoine, V; Rashid, W; Noyce, AJ; Silber, E; Morris, H; Giovannoni, G; Dobson, R (2023) ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK. BMJ Open, 13 (5). e071656. ISSN 2044-6055 https://doi.org/10.1136/bmjopen-2023-071656
SGUL Authors: Bezzina, Elizabeth Lindsey

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Abstract

PURPOSE: Genetic studies of multiple sclerosis (MS) susceptibility and severity have focused on populations of European ancestry. Studying MS genetics in other ancestral groups is necessary to determine the generalisability of these findings. The genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis (ADAMS) project aims to gather genetic and phenotypic data on a large cohort of ancestrally-diverse individuals with MS living in the UK. PARTICIPANTS: Adults with self-reported MS from diverse ancestral backgrounds. Recruitment is via clinical sites, online (https://app.mantal.co.uk/adams) or the UK MS Register. We are collecting demographic and phenotypic data using a baseline questionnaire and subsequent healthcare record linkage. We are collecting DNA from participants using saliva kits (Oragene-600) and genotyping using the Illumina Global Screening Array V.3. FINDINGS TO DATE: As of 3 January 2023, we have recruited 682 participants (n=446 online, n=55 via sites, n=181 via the UK MS Register). Of this initial cohort, 71.2% of participants are female, with a median age of 44.9 years at recruitment. Over 60% of the cohort are non-white British, with 23.5% identifying as Asian or Asian British, 16.2% as Black, African, Caribbean or Black British and 20.9% identifying as having mixed or other backgrounds. The median age at first symptom is 28 years, and median age at diagnosis is 32 years. 76.8% have relapsing-remitting MS, and 13.5% have secondary progressive MS. FUTURE PLANS: Recruitment will continue over the next 10 years. Genotyping and genetic data quality control are ongoing. Within the next 3 years, we aim to perform initial genetic analyses of susceptibility and severity with a view to replicating the findings from European-ancestry studies. In the long term, genetic data will be combined with other datasets to further cross-ancestry genetic discoveries.

Item Type: Article
Additional Information: © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
Keywords: GENETICS, Multiple sclerosis, Neurology, Adult, Humans, Female, Middle Aged, Male, Multiple Sclerosis, Multiple Sclerosis, Chronic Progressive, Multiple Sclerosis, Relapsing-Remitting, Genetic Association Studies, United Kingdom, Humans, Multiple Sclerosis, Multiple Sclerosis, Chronic Progressive, Multiple Sclerosis, Relapsing-Remitting, Adult, Middle Aged, Female, Male, Genetic Association Studies, United Kingdom, Multiple sclerosis, Neurology, GENETICS, 1103 Clinical Sciences, 1117 Public Health and Health Services, 1199 Other Medical and Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical, Biomedical and Allied Health Education (IMBE)
Academic Structure > Institute of Medical, Biomedical and Allied Health Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title: BMJ Open
ISSN: 2044-6055
Language: eng
Dates:
DateEvent
17 May 2023Published
14 April 2023Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MR/V028766/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
UNSPECIFIEDUK MS SocietyUNSPECIFIED
UNSPECIFIEDAims2Curehttps://doi.org/10.13039/100010255
UNSPECIFIEDBarts Charityhttps://doi.org/10.13039/100015652
PubMed ID: 37197821
Web of Science ID: WOS:001107086500009
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/117001
Publisher's version: https://doi.org/10.1136/bmjopen-2023-071656

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