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dc.contributor.authorWilliams, T
dc.contributor.authorJohn, N
dc.contributor.authorCalvi, A
dc.contributor.authorBianchi, A
dc.contributor.authorDe Angelis, F
dc.contributor.authorDoshi, A
dc.contributor.authorWright, S
dc.contributor.authorShatila, M
dc.contributor.authorYiannakas, MC
dc.contributor.authorChowdhury, F
dc.contributor.authorStutters, J
dc.contributor.authorRicciardi, A
dc.contributor.authorPrados, F
dc.contributor.authorMacManus, D
dc.contributor.authorBraisher, M
dc.contributor.authorBlackstone, J
dc.contributor.authorCiccarelli, O
dc.contributor.authorGandini Wheeler‐Kingshott, CAM
dc.contributor.authorBarkhof, F
dc.contributor.authorChataway, J
dc.date.accessioned2023-10-16T16:42:19Z
dc.date.issued2023-09
dc.identifier.issn1351-5101
dc.identifier.issn1468-1331
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/21448
dc.description.abstract

Background and purpose.There is increasing evidence that cardiovascular risk (CVR) contributes to disability progression in multiple sclerosis (MS). CVR is particularly prevalent in secondary progressive MS (SPMS) and can be quantified through validated composite CVR scores. The aim was to examine the cross‐sectional relationships between excess modifiable CVR, whole and regional brain atrophy on magnetic resonance imaging, and disability in patients with SPMS. Methods. Participants had SPMS, and data were collected at enrolment into the MS‐STAT2 trial. Composite CVR scores were calculated using the QRISK3 software. Prematurely achieved CVR due to modifiable risk factors was expressed as QRISK3 premature CVR, derived through reference to the normative QRISK3 dataset and expressed in years. Associations were determined with multiple linear regressions. Results. For the 218 participants, mean age was 54 years and median Expanded Disability Status Scale was 6.0. Each additional year of prematurely achieved CVR was associated with a 2.7 mL (beta coefficient; 95% confidence interval 0.8–4.7; p = 0.006) smaller normalized whole brain volume. The strongest relationship was seen for the cortical grey matter (beta coefficient 1.6 mL per year; 95% confidence interval 0.5–2.7; p = 0.003), and associations were also found with poorer verbal working memory performance. Body mass index demonstrated the strongest relationships with normalized brain volumes, whilst serum lipid ratios demonstrated strong relationships with verbal and visuospatial working memory performance. Conclusions. Prematurely achieved CVR is associated with lower normalized brain volumes in SPMS. Future longitudinal analyses of this clinical trial dataset will be important to determine whether CVR predicts future disease worsening.

dc.format.extent2769-2780
dc.format.mediumPrint-Electronic
dc.languageen
dc.publisherWiley
dc.subjectcardiovascular risk
dc.subjectcomorbidity
dc.subjectmultiple sclerosis
dc.subjectprogressive multiple sclerosis
dc.subjectsecondary progressive multiple sclerosis
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectMultiple Sclerosis
dc.subjectMultiple Sclerosis, Chronic Progressive
dc.subjectCardiovascular Diseases
dc.subjectCross-Sectional Studies
dc.subjectRisk Factors
dc.subjectBrain
dc.subjectMagnetic Resonance Imaging
dc.subjectMemory, Short-Term
dc.subjectHeart Disease Risk Factors
dc.subjectAtrophy
dc.subjectDisability Evaluation
dc.subjectDisease Progression
dc.subjectSTAT2 Transcription Factor
dc.titleCardiovascular risk factors in secondary progressive multiple sclerosis: A cross‐sectional analysis from the <scp>MS‐STAT2</scp> randomized controlled trial
dc.typejournal-article
dc.typeRandomized Controlled Trial
dc.typeJournal Article
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37318885
plymouth.issue9
plymouth.volume30
plymouth.publisher-urlhttp://dx.doi.org/10.1111/ene.15924
plymouth.publication-statusPublished
plymouth.journalEuropean Journal of Neurology
dc.identifier.doi10.1111/ene.15924
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Research Groups
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)|CCT&PS
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Medical School
dc.publisher.placeEngland
dcterms.dateAccepted2023-06-05
dc.date.updated2023-10-16T16:42:18Z
dc.rights.embargodate2023-10-17
dc.identifier.eissn1468-1331
rioxxterms.versionofrecord10.1111/ene.15924


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