The Gulf POMS evidence base is real but narrow, concentrated, and heterogeneous; a scoping review is currently the more informative synthesis than a quantitative meta-analysis, which supports a harmonized, multi-country Gulf pediatric MS registry with standardized outcome reporting, including neurocognitive and quality-of-life measures.
Abstract
Background: MS begins before age 18 in 3–10% of cases (pediatric-onset MS, POMS). Adult MS epidemiology is increasingly characterized across the Gulf, but whether the pediatric literature is sufficiently mature and ho0m1ogeneous to support a quantitative meta-analysis, as opposed to a scoping review, remains unclear. Objective: To map published POMS evidence across the six Gulf Cooperation Council (GCC) states and identify evidence gaps. Methods: A scoping review followed the Arksey and O’Malley framework, reported per PRISMA-ScR. Eligibility followed a Population-Concept-Context framework: MS onset before 18 years; epidemiological, clinical, diagnostic, therapeutic, and outcome data; the six GCC states. Adult-inclusive studies that did not report a dedicated pediatric-onset subgroup were retained only as contextual evidence and were not counted as meeting the Population criterion (see Methods). MEDLINE/PubMed, Embase, Scopus, Web of Science, and IMEMR were searched from inception through August 2026. Results: Eleven studies were included. Dedicated, pediatric-specific POMS data were identified from three of six countries: Kuwait (three epidemiological/clinical registry studies and two pediatric monoclonal-antibody outcome studies), Saudi Arabia (one national-registry study), and the UAE (two hospital/multicenter cohorts and one pediatric monoclonal-antibody outcome study). Qatar and Oman contributed only adult-inclusive prevalence studies without a dedicated pediatric subgroup, and no eligible study was identified from Bahrain. Incidence ranged from 2.1/100,000 (Kuwait) to a UAE-reported 7.2/100,000 in a 15–19-year age band that extends beyond the review’s < 18-year POMS definition; prevalence (2.7–36/100,000) was highest in the UAE. A relapsing–remitting course, female preponderance, and brainstem/cerebellar or visual presentations predominated; MRI, cognitive, and quality-of-life data were sparse or absent. Three studies reported pediatric natalizumab/ocrelizumab outcomes (Kuwait, UAE). Conclusion: The Gulf POMS evidence base is real but narrow, concentrated, and heterogeneous; a scoping review, which maps the evidence base and treats geographic and domain gaps as findings in their own right, is currently the more informative synthesis than a quantitative meta-analysis. This supports a harmonized, multi-country Gulf pediatric MS registry with standardized outcome reporting, including neurocognitive and quality-of-life measures.
This review summarizes the diagnostic work-up of children with a first acquired demyelinating syndrome, differential diagnosis, the role of MRI, cerebrospinal fluid (CSF) markers, antibody testing, serum neurofilament light chain, optical pathway assessment and the 2024 McDonald criteria.
M. Margoni, Massimo Filippi, M. Rocca· Expert Review of Neurotherap...· 0 citations
INTRODUCTION
Although there are extensive data on multiple sclerosis (MS) in adults, the epidemiology and clinical features of pediatric-onset multiple sclerosis (POMS) in Finland are unknown.
SUBJECTS
and methods: Individuals under 18 years of age diagnosed with clinically isolated syndrome (CIS) or MS were identifi...
Salla Hautala, Adrian Malén-Louekari, Mia Westerholm-Ormio et al.· European journal of paediatr...· 0 citations
Background Neuropsychiatric systemic lupus erythematosus (NPSLE) presents significant diagnostic and therapeutic challenges, particularly in childhood-onset SLE (cSLE), as there is limited pediatric-specific evidence, lack of specific diagnostic tests, and heavy reliance on adult data. This scoping review, the first de...
A. Theisen, E. Ogbu, Emily F. Beil et al.· Open Access Rheumatology : R...· 0 citations
Patients with LOMS tend to have a higher prevalence of PPMS, a greater burden of comorbidities, higher baseline disability, lower relapse activity, and a shorter time to CDP.
A. Fouad, Abdallah Saad, Hadeer Mohamed Abd El-Aziz et al.· Multiple Sclerosis and Relat...· 0 citations
OBJECTIVE
The objective of this scoping review was to synthesize evidence on the proportion of individuals living with Sjögren's disease who experience central nervous system (CNS) manifestations.
METHODS
We searched MEDLINE (via PubMed) and Embase from 1980 through January 29, 2026, and the ECRI Guidelines Trust fro...
A. Varadhachary, G. Noaiseh, J. Frantsve-Hawley et al.· Arthritis care & research· 0 citations
OBJECTIVE
Lennox-Gastaut syndrome (LGS) is a developmental and epileptic encephalopathy typically diagnosed in childhood. The 2022 International League Against Epilepsy (ILAE) criteria provide a diagnostic framework built on pediatric data, but their applicability in adulthood is challenged by disease evolution, treatm...
C. Liguori, S. Casciato, Emanuele Cerulli Irelli et al.· Epilepsia· 0 citations
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