ECTRIMS eLearning

Longitudinal follow-up of fatigue in CIS patients: a prospective study
Author(s): ,
R van der Vuurst de Vries
Affiliations:
Department of Neurology, MS centre ErasMS
,
J.J van den Dorpel
Affiliations:
Department of Neurology, MS centre ErasMS
,
J.Y Mescheriakova
Affiliations:
Department of Neurology, MS centre ErasMS
,
T.F Runia
Affiliations:
Department of Neurology, MS centre ErasMS
,
N Jafari
Affiliations:
Department of Neurology, MS centre ErasMS
,
T.A Siepman
Affiliations:
Department of Neurology, MS centre ErasMS
,
D Rizopoulos
Affiliations:
Department of Biostatistics
,
E.W Steyerberg
Affiliations:
Department of Public Health, Erasmus Medical Centre, Rotterdam, The Netherlands
R.Q Hintzen
Affiliations:
Department of Neurology, MS centre ErasMS
ECTRIMS Learn. van der Vuurst de Vries R. 09/15/16; 146146; P305
Roos van der Vuurst de Vries
Roos van der Vuurst de Vries
Contributions
Abstract

Abstract: P305

Type: Poster

Abstract Category: Clinical aspects of MS - Natural course

Background and Objective: Fatigue is a common symptom in MS, reported by more than 75% of MS patients. In an earlier study we showed that fatigue is not only a common symptom in patients at time of CIS (46%), but also predicts a subsequent diagnosis of CDMS and is associated with a shorter time to a next attack after CIS. Furthermore, in another study, fatigue in patients with MS has been found predictive of disease progression. The first aim of this study was to explore the longitudinal course of fatigue during follow-up after CIS. The second aim was to study the association of fatigue at time of CIS and disability when reaching MS diagnosis.

Methods: In this study 235 CIS patients, aged between 18 and 50 years, were prospectively followed. CIS patients with comorbidities other than depression, which are likely to cause fatigue, were excluded from the analysis. Patients filled in the Krupp"s Fatigue Severity Scale (FSS) at baseline and annually. When they reached CDMS diagnosis, EDSS was also obtained annually. Mixed effects models were used to analyse the longitudinal FSS measurements and to evaluate the association between the baseline FSS and EDSS during follow-up.

Results: In this prospective study 89 out of 235 CIS patients were diagnosed with CDMS (mean follow up 53.1 months (SD ±29.5)). Fatigue at baseline was validated as an independent predictor for CDMS (HR 2.9, 95% CI:1.8-4.9). At time of CIS, patients who were diagnosed with CDMS during follow-up had a significantly higher FSS score than monophasic CIS patients. We found a nonlinear average longitudinal evolution of FSS in time and this evolution was not altered after CDMS diagnosis (p=0.44). However, we found a significant increase of FSS score by 0.86 units when patients experienced a second attack after CIS (p=0.01). Additionally, we found that a high FSS score at baseline (>5.0) showed a trend towards a higher EDSS during follow-up (0.9 points higher EDSS) (p=0.1).

Conclusions: Fatigue, which is often present at time of CIS, persists over time and may increase after a second attack. A high FSS score at CIS might be associated with disability after CDMS diagnosis.

Disclosure:



RM van der Vuurst de Vries: nothing to disclose

JJA van den Dorpel: nothing to disclose

JY Mescheriakova: nothing to disclose

TF Runia: nothing to disclose

N Jafari: nothing to disclose

DAM Siepman: nothing to disclose

D Rizopoulos: nothing to disclose

EW Steyerberg: nothing to disclose

RQ Hintzen: nothing to disclose





Funding

The study was supported by the Dutch MS research Foundation.

Abstract: P305

Type: Poster

Abstract Category: Clinical aspects of MS - Natural course

Background and Objective: Fatigue is a common symptom in MS, reported by more than 75% of MS patients. In an earlier study we showed that fatigue is not only a common symptom in patients at time of CIS (46%), but also predicts a subsequent diagnosis of CDMS and is associated with a shorter time to a next attack after CIS. Furthermore, in another study, fatigue in patients with MS has been found predictive of disease progression. The first aim of this study was to explore the longitudinal course of fatigue during follow-up after CIS. The second aim was to study the association of fatigue at time of CIS and disability when reaching MS diagnosis.

Methods: In this study 235 CIS patients, aged between 18 and 50 years, were prospectively followed. CIS patients with comorbidities other than depression, which are likely to cause fatigue, were excluded from the analysis. Patients filled in the Krupp"s Fatigue Severity Scale (FSS) at baseline and annually. When they reached CDMS diagnosis, EDSS was also obtained annually. Mixed effects models were used to analyse the longitudinal FSS measurements and to evaluate the association between the baseline FSS and EDSS during follow-up.

Results: In this prospective study 89 out of 235 CIS patients were diagnosed with CDMS (mean follow up 53.1 months (SD ±29.5)). Fatigue at baseline was validated as an independent predictor for CDMS (HR 2.9, 95% CI:1.8-4.9). At time of CIS, patients who were diagnosed with CDMS during follow-up had a significantly higher FSS score than monophasic CIS patients. We found a nonlinear average longitudinal evolution of FSS in time and this evolution was not altered after CDMS diagnosis (p=0.44). However, we found a significant increase of FSS score by 0.86 units when patients experienced a second attack after CIS (p=0.01). Additionally, we found that a high FSS score at baseline (>5.0) showed a trend towards a higher EDSS during follow-up (0.9 points higher EDSS) (p=0.1).

Conclusions: Fatigue, which is often present at time of CIS, persists over time and may increase after a second attack. A high FSS score at CIS might be associated with disability after CDMS diagnosis.

Disclosure:



RM van der Vuurst de Vries: nothing to disclose

JJA van den Dorpel: nothing to disclose

JY Mescheriakova: nothing to disclose

TF Runia: nothing to disclose

N Jafari: nothing to disclose

DAM Siepman: nothing to disclose

D Rizopoulos: nothing to disclose

EW Steyerberg: nothing to disclose

RQ Hintzen: nothing to disclose





Funding

The study was supported by the Dutch MS research Foundation.

By clicking “Accept Terms & all Cookies” or by continuing to browse, you agree to the storing of third-party cookies on your device to enhance your user experience and agree to the user terms and conditions of this learning management system (LMS).

Cookie Settings
Accept Terms & all Cookies