Journal Article

Brain reserve and physical disability in secondary progressive multiple sclerosis

Mollison, Daisy, Stutters, Jonathan, Colville, Shuna, Craner, Matthew, Ford, Helen, Braisher, Marie, Paling, David, Doshi, Anisha, Phan, Thanh, Hawkins, Clive, Smith, Lorraine, Palace, Jacqueline, Barkhof, Frederik, Nicholas, Richard, Beyene, Tiggy, Gnanapavan, Sharmilee, Li, Yingtong, Bastow, Roger, Arndt, Heinke, Guadagno, Joe, McLean, Brendan, Evangelou, Nikolaos, Calvi, Alberto, Hobart, Jeremy, Dhillon, Baljean, Cameron, James, Stallard, Nigel, Ourselin, Sebastien, John, Nevin, Overell, James, Pavitt, Sue H, Ross, Moira, Walker, Allan, Chataway, Jeremy, Bassan, Vanessa, Aram, Julia, Rashid, Waqar, Plantone, Domenico, Kalra, Seema, Young, Carolyn, Prados Carrasco, Ferran, Eshaghi, Arman, Giovannoni, Gavin, Williams, Thomas, Chandran, Siddharthan, Lyle, Dawn, Zapata, Alvin, Sharrack, Basil, De Angelis, Floriana, Connick, Peter, Duddy, Martin, Cranswick, Gina

2024

Overview

BackgroundThe brain reserve hypothesis posits that larger maximal lifetime brain growth (MLBG) may confer protection against physical disability in multiple sclerosis (MS). Larger MLBG as a proxy for brain reserve, has been associated with reduced progression of physical disability in patients with early MS; however, it is unknown whether this association remains once in the secondary progressive phase of MS (SPMS). Our aim was to assess whether larger MLBG is associated with decreased physical disability progression in SPMS.MethodsWe conducted a post hoc analysis of participants in the MS-Secondary Progressive Multi-Arm Randomisation Trial (NCT01910259), a multicentre randomised placebo-controlled trial of the neuroprotective potential of three agents in SPMS. Physical disability was measured by Expanded Disability Status Scale (EDSS), 9-hole peg test (9HPT) and 25-foot timed walk test (T25FW) at baseline, 48 and 96 weeks. MLBG was estimated by baseline intracranial volume (ICV). Multivariable time-varying Cox regression models were used to investigate the association between MLBG and physical disability progression.Results383 participants (mean age 54.5 years, 298 female) were followed up over 96 weeks. Median baseline EDSS was 6.0 (range 4.0–6.5). Adjusted for covariates, larger MLBG was associated with a reduced risk of EDSS progression (HR 0.84,95% CI:0.72 to 0.99;p=0.04). MLBG was not independently associated with time to progression as measured by 9HPT or T25FW.ConclusionLarger MLBG is independently associated with physical disability progression over 96 weeks as measured by EDSS in SPMS. This suggests that MLBG as a proxy for brain reserve may continue to confer protection against disability when in the secondary progression phase of MS.Trail registration numberNCT01910259.

• Publisher: BMJ Publishing Group Ltd,BMJ Publishing Group LTD,BMJ Publishing Group
• Subject: Age / Brain research / Cross-sectional studies / Dementia / Hypotheses / MULTIPLE SCLEROSIS / NEUROIMMUNOLOGY / Original Research / Pathology