Evidence map›Paper›PMID 42753010›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Impact of age, BMI, and renal function adjustment on interpretation of serum NfL and GFAP in multiple sclerosis progression: a scoping review.

Aziza Shavkatovna Kadirova, Gulnora Kutpitdinovna Rakhmatullaeva, Javlon Jasur Ugli Salimjonov

Abstract readScoping Review
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Aziza Shavkatovna KadirovaDepartment of Medical Rehabilitation, Neurology and Sports Medicine, Tashkent State Medical University, Tashkent, Uzbekistan. azizka_k@mail.ru.ORCID http://orcid.org/0009-0008-3734-3548
Gulnora Kutpitdinovna RakhmatullaevaDepartment of Medical Rehabilitation, Neurology and Sports Medicine, Tashkent State Medical University, Tashkent, Uzbekistan.ORCID http://orcid.org/0000-0001-5932-7911
Javlon Jasur Ugli SalimjonovDepartment of Medical Rehabilitation, Neurology and Sports Medicine, Tashkent State Medical University, Tashkent, Uzbekistan.ORCID http://orcid.org/0009-0000-7199-0310

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite achieving NEDA‑3, a substantial proportion of patients with multiple sclerosis (MS) accumulate disability through progression independent of relapse activity (PIRA). This scoping review evaluates serum neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) in relation to disease activity and progression, with particular focus on the effects of age, BMI, and renal function on biomarker interpretation.

methodsThe review followed PRISMA‑ScR guidelines (PubMed, Scopus, Web of Science, January 2016 - February 2026). Longitudinal studies (≥ 12 months) with multivariable adjustment were prioritised. Of 467 screened records, 367 were excluded; 100 full‑text articles were assessed. Of these, 36 were excluded. Sixty‑four publications were included; 34 original analytical studies formed the basis of the structured synthesis.

resultssNfL was consistently associated with acute inflammatory activity, whereas associations with progression were less consistent after adjustment for age and other covariates. sGFAP showed stronger associations with PIRA and disability progression in several longitudinal studies, although findings were heterogeneous. PIRA definitions and follow-up durations varied substantially, limiting direct comparability. Evidence regarding renal-function adjustment was limited and heterogeneous: adjustment attenuated the association between sGFAP and progression in one study, whereas associations remained evident in other studies accounting for renal function.

conclusionsAge, BMI, and renal function should be considered when interpreting circulating NfL and GFAP, particularly in studies of progression. The available evidence does not support universal biomarker cut-offs or uniform interpretation of PIRA-associated concentrations. Prospective studies with harmonised PIRA definitions, sufficiently long follow-up, and consistent confounder adjustment are needed.

Indexed as

Body Mass IndexDisease ProgressionGlial Fibrillary Acidic ProteinMultiple SclerosisNeurofilament ProteinsAge FactorsBiomarkersHumansBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament ProteinsConfoundersGlial fibrillary acidic proteinMultiple sclerosisNeurofilament light chainProgression independent of relapse activityResearch framework

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.