Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality

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Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality. / Thormann, Anja; Sørensen, Per Soelberg; Koch-Henriksen, Nils; Laursen, Bjarne; Magyari, Melinda.

In: Neurology, Vol. 89, No. 16, 17.10.2017, p. 1668-1675.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Thormann, A, Sørensen, PS, Koch-Henriksen, N, Laursen, B & Magyari, M 2017, 'Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality', Neurology, vol. 89, no. 16, pp. 1668-1675. https://doi.org/10.1212/WNL.0000000000004508

APA

Thormann, A., Sørensen, P. S., Koch-Henriksen, N., Laursen, B., & Magyari, M. (2017). Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality. Neurology, 89(16), 1668-1675. https://doi.org/10.1212/WNL.0000000000004508

Vancouver

Thormann A, Sørensen PS, Koch-Henriksen N, Laursen B, Magyari M. Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality. Neurology. 2017 Oct 17;89(16):1668-1675. https://doi.org/10.1212/WNL.0000000000004508

Author

Thormann, Anja ; Sørensen, Per Soelberg ; Koch-Henriksen, Nils ; Laursen, Bjarne ; Magyari, Melinda. / Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality. In: Neurology. 2017 ; Vol. 89, No. 16. pp. 1668-1675.

Bibtex

@article{8940d75712b946a0b1cf98bf7ff2a377,
title = "Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality",
abstract = "Objective: To investigate the effect of chronic comorbidity on the time of diagnosis of multiple sclerosis (MS) and on mortality in MS. Methods: We conducted a population-based, nationwide cohort study including all incident MS cases in Denmark with first MS symptom between 1980 and 2005. To investigate the time of diagnosis, we compared individuals with and without chronic comorbidity using multinomial logistic regression. To investigate mortality, we used Cox regression with time-dependent covariates, following study participants from clinical MS onset until endpoint (death) or to the end of the study, censuring at emigration. Results: We identified 8,947 individuals with clinical onset of MS between 1980 and 2005. In the study of time of diagnosis, we found statistically significant odds ratios for longer diagnostic delays with cerebrovascular comorbidity (2.01 [1.44-2.80]; <0.0005), cardiovascular comorbidity (4.04 [2.78-5.87]; <0.0005), lung comorbidity (1.93 [1.42-2.62]; <0.0005), diabetes comorbidity (1.78 [1.04-3.06]; 0.035), and cancer comorbidity (2.10 [1.20-3.67]; 0.009). In the mortality study, we found higher hazard ratios with psychiatric comorbidity (2.42 [1.67-3.01]; <0.0005), cerebrovascular comorbidity (2.47 [2.05-2.79]; <0.0005), cardiovascular comorbidity (1.68 [1.39-2.03]; <0.0005), lung comorbidity (1.23 [1.01-1.50]; 0.036), diabetes comorbidity (1.39 [1.05-1.85]; 0.021), cancer comorbidity (3.51 [2.94-4.19]; <0.0005), and Parkinson disease comorbidity (2.85 [1.34-6.06]; 0.007). Conclusions: An increased awareness of both the necessity of neurologic evaluation of new neurologic symptoms in persons with preexisting chronic disease and of optimum treatment of comorbidity in MS is critical.",
author = "Anja Thormann and S{\o}rensen, {Per Soelberg} and Nils Koch-Henriksen and Bjarne Laursen and Melinda Magyari",
year = "2017",
month = oct,
day = "17",
doi = "10.1212/WNL.0000000000004508",
language = "English",
volume = "89",
pages = "1668--1675",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott Williams & Wilkins",
number = "16",

}

RIS

TY - JOUR

T1 - Comorbidity in multiple sclerosis is associated with diagnostic delays and increased mortality

AU - Thormann, Anja

AU - Sørensen, Per Soelberg

AU - Koch-Henriksen, Nils

AU - Laursen, Bjarne

AU - Magyari, Melinda

PY - 2017/10/17

Y1 - 2017/10/17

N2 - Objective: To investigate the effect of chronic comorbidity on the time of diagnosis of multiple sclerosis (MS) and on mortality in MS. Methods: We conducted a population-based, nationwide cohort study including all incident MS cases in Denmark with first MS symptom between 1980 and 2005. To investigate the time of diagnosis, we compared individuals with and without chronic comorbidity using multinomial logistic regression. To investigate mortality, we used Cox regression with time-dependent covariates, following study participants from clinical MS onset until endpoint (death) or to the end of the study, censuring at emigration. Results: We identified 8,947 individuals with clinical onset of MS between 1980 and 2005. In the study of time of diagnosis, we found statistically significant odds ratios for longer diagnostic delays with cerebrovascular comorbidity (2.01 [1.44-2.80]; <0.0005), cardiovascular comorbidity (4.04 [2.78-5.87]; <0.0005), lung comorbidity (1.93 [1.42-2.62]; <0.0005), diabetes comorbidity (1.78 [1.04-3.06]; 0.035), and cancer comorbidity (2.10 [1.20-3.67]; 0.009). In the mortality study, we found higher hazard ratios with psychiatric comorbidity (2.42 [1.67-3.01]; <0.0005), cerebrovascular comorbidity (2.47 [2.05-2.79]; <0.0005), cardiovascular comorbidity (1.68 [1.39-2.03]; <0.0005), lung comorbidity (1.23 [1.01-1.50]; 0.036), diabetes comorbidity (1.39 [1.05-1.85]; 0.021), cancer comorbidity (3.51 [2.94-4.19]; <0.0005), and Parkinson disease comorbidity (2.85 [1.34-6.06]; 0.007). Conclusions: An increased awareness of both the necessity of neurologic evaluation of new neurologic symptoms in persons with preexisting chronic disease and of optimum treatment of comorbidity in MS is critical.

AB - Objective: To investigate the effect of chronic comorbidity on the time of diagnosis of multiple sclerosis (MS) and on mortality in MS. Methods: We conducted a population-based, nationwide cohort study including all incident MS cases in Denmark with first MS symptom between 1980 and 2005. To investigate the time of diagnosis, we compared individuals with and without chronic comorbidity using multinomial logistic regression. To investigate mortality, we used Cox regression with time-dependent covariates, following study participants from clinical MS onset until endpoint (death) or to the end of the study, censuring at emigration. Results: We identified 8,947 individuals with clinical onset of MS between 1980 and 2005. In the study of time of diagnosis, we found statistically significant odds ratios for longer diagnostic delays with cerebrovascular comorbidity (2.01 [1.44-2.80]; <0.0005), cardiovascular comorbidity (4.04 [2.78-5.87]; <0.0005), lung comorbidity (1.93 [1.42-2.62]; <0.0005), diabetes comorbidity (1.78 [1.04-3.06]; 0.035), and cancer comorbidity (2.10 [1.20-3.67]; 0.009). In the mortality study, we found higher hazard ratios with psychiatric comorbidity (2.42 [1.67-3.01]; <0.0005), cerebrovascular comorbidity (2.47 [2.05-2.79]; <0.0005), cardiovascular comorbidity (1.68 [1.39-2.03]; <0.0005), lung comorbidity (1.23 [1.01-1.50]; 0.036), diabetes comorbidity (1.39 [1.05-1.85]; 0.021), cancer comorbidity (3.51 [2.94-4.19]; <0.0005), and Parkinson disease comorbidity (2.85 [1.34-6.06]; 0.007). Conclusions: An increased awareness of both the necessity of neurologic evaluation of new neurologic symptoms in persons with preexisting chronic disease and of optimum treatment of comorbidity in MS is critical.

U2 - 10.1212/WNL.0000000000004508

DO - 10.1212/WNL.0000000000004508

M3 - Journal article

C2 - 28931645

AN - SCOPUS:85031403481

VL - 89

SP - 1668

EP - 1675

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 16

ER -

ID: 193581553