ECTRIMS eLearning

Predicting paediatric multiple sclerosis in 'MRI negative' patients: bands do aid
Author(s): ,
Y.Y.M Wong
Affiliations:
Neurology, Erasmus MC, Rotterdam, The Netherlands
,
L.H Verhey
Affiliations:
Pediatrics and Research Institute, The Hospital for Sick Children, Toronto, ON, Canada
,
E.D van Pelt
Affiliations:
Neurology, Erasmus MC, Rotterdam, The Netherlands
,
J O'Mahony
Affiliations:
Pediatrics and Research Institute, The Hospital for Sick Children, Toronto, ON, Canada
,
I.A Ketelslegers
Affiliations:
Neurology, Erasmus MC, Rotterdam, The Netherlands
,
R.F Neuteboom
Affiliations:
Pediatric Neurology, Erasmus MC, Rotterdam, The Netherlands
,
C.E Catsman-Berrevoets
Affiliations:
Pediatric Neurology, Erasmus MC, Rotterdam, The Netherlands
,
D.L Arnold
Affiliations:
Neurology, Montreal Neurological Institute, Montreal, QC, Canada
,
A Bar-Or
Affiliations:
Neurology, Montreal Neurological Institute, Montreal, QC, Canada
,
B.L Banwell
Affiliations:
Neurology, The Children's hospital of Philadelphia, Philadelphia, PA, United States
,
R.Q Hintzen
Affiliations:
Neurology, Erasmus MC, Rotterdam, The Netherlands
the Dutch Paediatric MS Study Group, the Canadian Paediatric Demyelinating Disease Network.
the Dutch Paediatric MS Study Group, the Canadian Paediatric Demyelinating Disease Network.
Affiliations:
ECTRIMS Learn. Wong Y. 09/16/16; 146668; P828
Yu Yi M. Wong
Yu Yi M. Wong
Contributions
Abstract

Abstract: P828

Type: Poster

Abstract Category: Clinical aspects of MS - Paediatric MS

Introduction: A first demyelinating event in the central nervous system in children might be the first presentation of paediatric-onset multiple sclerosis (POMS). The Verhey criteria showed high predictive value for POMS in both Canadian and Dutch ADS cohorts. However, in clinical practice one is likely to encounter patients who, at clinical onset, do not fulfill McDonald 2010 criteria and are in addition negative for one or both items of the Verhey criteria. Our aim is to investigate whether OCB may be of additional diagnostic value for predicting clinically definite MS (CDMS) in paediatric patients with acquired demyelinating syndromes (ADS) who are negative for both MRI criteria at incident presentation.

Methods: Children in the Canadian and Dutch prospective ADS databases were eligible for this study if the first MRI and OCB result were both available. MRI scans at onset were evaluated according to the Verhey MRI criteria and the McDonald 2010 MRI criteria. OCB status was tested locally with isoelectric focusing in 109/113 (96%) of cases. A minimal follow-up of two years was required for inclusion, unless the patient was diagnosed with CDMS in this period. Statistical analysis was performed with Chi square, Mann-Whitney U test and the logistic regression model.

Results: One hundred and thirteen ADS patients were included who were negative for both MRI criteria. Fourteen developed CDMS. The CDMS group was significantly older (median age 14.8 years) and had more often OCB positivity than the non-CDMS group (86% vs 13%).

OCB positivity was found in 25/113 of the ADS patients of whom 12/25 (48%) developed CDMS, in contrast to 2/88 (2%) of patients without OCB. The negative predictive value of OCB was high (97%). In a logistic regression model, OCB showed a high odds ratio of 35.3 (95% CI 4.1-307.1, p< 0.000), after correction for the presence of encephalopathy, optic neuritis presenting phenotype, age of onset, gender and abnormal MRI with presence of T2/FLAIR lesions.

Conclusion: OCB in CSF can aid in prediction of POMS in patients who are negative at onset for McDonald 2010 and Verhey MRI criteria. This is most appreciated in patients with a negative OCB status. These patients have a very low risk of MS diagnosis.

Disclosure: YYM Wong: nothing to disclose

LH Verhey: nothing to disclose

ED van Pelt: nothing to disclose

J O"Mahony: nothing to disclose

IA Ketelslegers: nothing to disclose

RF Neuteboom: nothing to disclose

CE Catsman-Berrevoets: nothing to disclose

DL Arnold: nothing to disclose

A Bar-Or: nothing to disclose

BL Banwell: nothing to disclose

RQ Hintzen: nothing to disclose



This study was supported by the Dutch and Canadian Multiple Sclerosis research foundation

Abstract: P828

Type: Poster

Abstract Category: Clinical aspects of MS - Paediatric MS

Introduction: A first demyelinating event in the central nervous system in children might be the first presentation of paediatric-onset multiple sclerosis (POMS). The Verhey criteria showed high predictive value for POMS in both Canadian and Dutch ADS cohorts. However, in clinical practice one is likely to encounter patients who, at clinical onset, do not fulfill McDonald 2010 criteria and are in addition negative for one or both items of the Verhey criteria. Our aim is to investigate whether OCB may be of additional diagnostic value for predicting clinically definite MS (CDMS) in paediatric patients with acquired demyelinating syndromes (ADS) who are negative for both MRI criteria at incident presentation.

Methods: Children in the Canadian and Dutch prospective ADS databases were eligible for this study if the first MRI and OCB result were both available. MRI scans at onset were evaluated according to the Verhey MRI criteria and the McDonald 2010 MRI criteria. OCB status was tested locally with isoelectric focusing in 109/113 (96%) of cases. A minimal follow-up of two years was required for inclusion, unless the patient was diagnosed with CDMS in this period. Statistical analysis was performed with Chi square, Mann-Whitney U test and the logistic regression model.

Results: One hundred and thirteen ADS patients were included who were negative for both MRI criteria. Fourteen developed CDMS. The CDMS group was significantly older (median age 14.8 years) and had more often OCB positivity than the non-CDMS group (86% vs 13%).

OCB positivity was found in 25/113 of the ADS patients of whom 12/25 (48%) developed CDMS, in contrast to 2/88 (2%) of patients without OCB. The negative predictive value of OCB was high (97%). In a logistic regression model, OCB showed a high odds ratio of 35.3 (95% CI 4.1-307.1, p< 0.000), after correction for the presence of encephalopathy, optic neuritis presenting phenotype, age of onset, gender and abnormal MRI with presence of T2/FLAIR lesions.

Conclusion: OCB in CSF can aid in prediction of POMS in patients who are negative at onset for McDonald 2010 and Verhey MRI criteria. This is most appreciated in patients with a negative OCB status. These patients have a very low risk of MS diagnosis.

Disclosure: YYM Wong: nothing to disclose

LH Verhey: nothing to disclose

ED van Pelt: nothing to disclose

J O"Mahony: nothing to disclose

IA Ketelslegers: nothing to disclose

RF Neuteboom: nothing to disclose

CE Catsman-Berrevoets: nothing to disclose

DL Arnold: nothing to disclose

A Bar-Or: nothing to disclose

BL Banwell: nothing to disclose

RQ Hintzen: nothing to disclose



This study was supported by the Dutch and Canadian Multiple Sclerosis research foundation

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