Smoking, obesity, and disability worsening in PPMS: an analysis of the INFORMS original trial dataset.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 02 07 2021
accepted: 06 08 2021
revised: 30 07 2021
pubmed: 16 8 2021
medline: 23 2 2022
entrez: 15 8 2021
Statut: ppublish

Résumé

Smoking and obesity are recognized modifiable risk factors associated with a higher MS incidence, but their impact on physical and cognitive disability worsening is less clear. To investigate the impact of smoking and obesity on disability worsening in primary progressive MS (PPMS). We used data from INFORMS (clinicaltrials.gov identifier: NCT00731692), a large randomized-controlled trial in PPMS to compare significant worsening on the EDSS, T25FW, NHPT, and PASAT between smokers and non-smokers, and between BMI groups, at 12, 24, and 33 months of follow-up. We investigated the association of smoking and BMI at screening and the risk of disability worsening with logistic regression models. Smokers had significantly higher EDSS scores throughout the trial. EDSS was not significantly different between BMI categories. No other outcome measure was significantly different between smokers and non-smokers and between BMI categories throughout the trial. Neither smoking status nor BMI were associated with significant worsening on any outcome measure at any time point during follow-up. Despite the known effects on MS incidence, smoking and BMI were not associated with the risk of physical and cognitive disability worsening over 3 years in this well-characterized PPMS trial cohort.

Sections du résumé

BACKGROUND BACKGROUND
Smoking and obesity are recognized modifiable risk factors associated with a higher MS incidence, but their impact on physical and cognitive disability worsening is less clear.
OBJECTIVE OBJECTIVE
To investigate the impact of smoking and obesity on disability worsening in primary progressive MS (PPMS).
METHODS METHODS
We used data from INFORMS (clinicaltrials.gov identifier: NCT00731692), a large randomized-controlled trial in PPMS to compare significant worsening on the EDSS, T25FW, NHPT, and PASAT between smokers and non-smokers, and between BMI groups, at 12, 24, and 33 months of follow-up. We investigated the association of smoking and BMI at screening and the risk of disability worsening with logistic regression models.
RESULTS RESULTS
Smokers had significantly higher EDSS scores throughout the trial. EDSS was not significantly different between BMI categories. No other outcome measure was significantly different between smokers and non-smokers and between BMI categories throughout the trial. Neither smoking status nor BMI were associated with significant worsening on any outcome measure at any time point during follow-up.
CONCLUSION CONCLUSIONS
Despite the known effects on MS incidence, smoking and BMI were not associated with the risk of physical and cognitive disability worsening over 3 years in this well-characterized PPMS trial cohort.

Identifiants

pubmed: 34392376
doi: 10.1007/s00415-021-10750-z
pii: 10.1007/s00415-021-10750-z
doi:

Banques de données

ClinicalTrials.gov
['NCT00731692']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1663-1669

Informations de copyright

© 2021. Springer-Verlag GmbH Germany, part of Springer Nature.

Références

Koch M, Mostert J, Heersema D, De Keyser J (2007) Progression in multiple sclerosis: further evidence of an age dependent process. J Neurol Sci 255:35–41. https://doi.org/10.1016/j.jns.2007.01.067
doi: 10.1016/j.jns.2007.01.067 pubmed: 17331540
Vukusic S, Confavreux C (2007) Natural history of multiple sclerosis: risk factors and prognostic indicators. Curr Opin Neurol 20:269–274. https://doi.org/10.1097/WCO.0b013e32812583ad
doi: 10.1097/WCO.0b013e32812583ad pubmed: 17495619
Hernán MA, Olek MJ, Ascherio A (2001) Cigarette smoking and incidence of multiple sclerosis. Am J Epidemiol 154:69–74
doi: 10.1093/aje/154.1.69
Handel AE, Williamson AJ, Disanto G et al (2011) Smoking and multiple sclerosis: an updated meta-analysis. PLoS ONE 6:e16149. https://doi.org/10.1371/journal.pone.0016149
doi: 10.1371/journal.pone.0016149 pubmed: 21249154 pmcid: 3020969
Cortese M, Riise T, Bjørnevik K et al (2018) Body size and physical exercise, and the risk of multiple sclerosis. Mult Scler 24:270–278. https://doi.org/10.1177/1352458517699289
doi: 10.1177/1352458517699289 pubmed: 28287051
Gianfrancesco MA, Stridh P, Rhead B et al (2017) Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS. Neurology 88:1623–1629. https://doi.org/10.1212/WNL.0000000000003849
doi: 10.1212/WNL.0000000000003849 pubmed: 28356466 pmcid: 5405763
Hernán MA, Jick SS, Logroscino G et al (2005) Cigarette smoking and the progression of multiple sclerosis. Brain 128:1461–1465. https://doi.org/10.1093/brain/awh471
doi: 10.1093/brain/awh471 pubmed: 15758034
Healy BC, Ali EN, Guttmann CRG et al (2009) Smoking and disease progression in multiple sclerosis. Arch Neurol 66:858–864. https://doi.org/10.1001/archneurol.2009.122
doi: 10.1001/archneurol.2009.122 pubmed: 19597087 pmcid: 2754172
Koch M, van Harten A, Uyttenboogaart M, De Keyser J (2007) Cigarette smoking and progression in multiple sclerosis. Neurology 69:1515–1520. https://doi.org/10.1212/01.wnl.0000277658.78381.db
doi: 10.1212/01.wnl.0000277658.78381.db pubmed: 17923613
Javizian O, Metz LM, Deighton S, Koch MW (2017) Smoking does not influence disability accumulation in primary progressive multiple sclerosis. Eur J Neurol 24:624–630. https://doi.org/10.1111/ene.13262
doi: 10.1111/ene.13262 pubmed: 28239937
Lublin F, Miller DH, Freedman MS et al (2016) Oral fingolimod in primary progressive multiple sclerosis (INFORMS): a phase 3, randomised, double-blind, placebo-controlled trial. Lancet 387:1075–1084. https://doi.org/10.1016/S0140-6736(15)01314-8
doi: 10.1016/S0140-6736(15)01314-8 pubmed: 26827074
Motl RW, Cohen JA, Benedict R et al (2017) Validity of the timed 25-foot walk as an ambulatory performance outcome measure for multiple sclerosis. Mult Scler 23:704–710. https://doi.org/10.1177/1352458517690823
doi: 10.1177/1352458517690823 pubmed: 28206828 pmcid: 5405807
Feys P, Lamers I, Francis G et al (2017) The Nine-Hole Peg Test as a manual dexterity performance measure for multiple sclerosis. Mult Scler 23:711–720. https://doi.org/10.1177/1352458517690824
doi: 10.1177/1352458517690824 pubmed: 28206826 pmcid: 5405844
R Core Team (2021) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna
Barros AJD, Hirakata VN (2003) Alternatives for logistic regression in cross-sectional studies: an empirical comparison of models that directly estimate the prevalence ratio. BMC Med Res Methodol 3:21. https://doi.org/10.1186/1471-2288-3-21
doi: 10.1186/1471-2288-3-21 pubmed: 14567763 pmcid: 521200
Hedström AK, Bäärnhielm M, Olsson T, Alfredsson L (2011) Exposure to environmental tobacco smoke is associated with increased risk for multiple sclerosis. Mult Scler 17:788–793. https://doi.org/10.1177/1352458511399610
doi: 10.1177/1352458511399610 pubmed: 21372120
Hedström AK, Olsson T, Alfredsson L (2016) Body mass index during adolescence, rather than childhood, is critical in determining MS risk. Mult Scler 22:878–883. https://doi.org/10.1177/1352458515603798
doi: 10.1177/1352458515603798 pubmed: 26362895
Briggs FBS, Thompson NR, Conway DS (2019) Prognostic factors of disability in relapsing remitting multiple sclerosis. Mult Scler Relat Disord 30:9–16. https://doi.org/10.1016/j.msard.2019.01.045
doi: 10.1016/j.msard.2019.01.045 pubmed: 30711764
Fitzgerald KC, Salter A, Tyry T et al (2020) Measures of general and abdominal obesity and disability severity in a large population of people with multiple sclerosis. Mult Scler 26:976–986. https://doi.org/10.1177/1352458519845836
doi: 10.1177/1352458519845836 pubmed: 31079537
Filippatou AG, Lambe J, Sotirchos ES et al (2020) Association of body mass index with longitudinal rates of retinal atrophy in multiple sclerosis. Mult Scler 26:843–854. https://doi.org/10.1177/1352458519900942
doi: 10.1177/1352458519900942 pubmed: 32297826 pmcid: 7293552
Mowry EM, Azevedo CJ, McCulloch CE et al (2018) Body mass index, but not vitamin D status, is associated with brain volume change in MS. Neurology 91:e2256–e2264. https://doi.org/10.1212/WNL.0000000000006644
doi: 10.1212/WNL.0000000000006644 pubmed: 30429274 pmcid: 6329329
Owji M, Ashraf-Ganjouei A, Sahraian MA et al (2019) The relationship between cognitive function and body mass index in multiple sclerosis patients. Mult Scler Relat Disord 32:37–40. https://doi.org/10.1016/j.msard.2019.04.024
doi: 10.1016/j.msard.2019.04.024 pubmed: 31030017
Cortese M, Munger KL, Martínez-Lapiscina EH et al (2020) Vitamin D, smoking, EBV, and long-term cognitive performance in MS: 11-year follow-up of BENEFIT. Neurology 94:e1950–e1960. https://doi.org/10.1212/WNL.0000000000009371
doi: 10.1212/WNL.0000000000009371 pubmed: 32300060 pmcid: 7274920
Kutzelnigg A, Lucchinetti CF, Stadelmann C et al (2005) Cortical demyelination and diffuse white matter injury in multiple sclerosis. Brain 128:2705–2712. https://doi.org/10.1093/brain/awh641
doi: 10.1093/brain/awh641 pubmed: 16230320
Frischer JM, Bramow S, Dal-Bianco A et al (2009) The relation between inflammation and neurodegeneration in multiple sclerosis brains. Brain 132:1175–1189. https://doi.org/10.1093/brain/awp070
doi: 10.1093/brain/awp070 pubmed: 19339255 pmcid: 2677799
Lassmann H, van Horssen J, Mahad D (2012) Progressive multiple sclerosis: pathology and pathogenesis. Nat Rev Neurol 8:647–656. https://doi.org/10.1038/nrneurol.2012.168
doi: 10.1038/nrneurol.2012.168 pubmed: 23007702
Confavreux C, Vukusic S, Adeleine P (2003) Early clinical predictors and progression of irreversible disability in multiple sclerosis: an amnesic process. Brain 126:770–782
doi: 10.1093/brain/awg081
Leray E, Yaouanq J, Le Page E et al (2010) Evidence for a two-stage disability progression in multiple sclerosis. Brain 133:1900–1913. https://doi.org/10.1093/brain/awq076
doi: 10.1093/brain/awq076 pubmed: 20423930 pmcid: 2892936

Auteurs

Marcus W Koch (MW)

Department of Clinical Neurosciences, University of Calgary, Calgary, Canada. mwkoch@ucalgary.ca.
Department of Community Health Sciences, University of Calgary, Calgary, Canada. mwkoch@ucalgary.ca.

Jop Mostert (J)

Department of Neurology, Rijnstate Hospital, Arnhem, The Netherlands.

Pavle Repovic (P)

Multiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, USA.

James D Bowen (JD)

Multiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, USA.

Eva Strijbis (E)

Department of Neurology, MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Bernard Uitdehaag (B)

Department of Neurology, MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Gary Cutter (G)

Department of Biostatistics, University of Alabama at Birmingham, Birmingham, USA.

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