Evidence map›Paper›PMID 40265739›Full record

ArticleAnnals of Indian Academy of Neurology2025

Efficacy of Subcutaneous and Intravenous Immunoglobulin in Patients with Multifocal Motor Neuropathy: A Systematic Review and Meta-analysis.

Indar Kumar Sharawat, Pragnya Panda, Lesa Dawman, Ananthanarayanan Kasinathan, Prateek Kumar Panda

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Article in Annals of Indian Academy of Neurology, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Indar Kumar SharawatDepartment of Pediatrics, Pediatric Neurology Division and Evidence Synthesis Unit, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Pragnya PandaDepartment of Neurology, All India Institute of Medical Sciences, Raebareli, Uttar Pradesh, India.
Lesa DawmanDepartment of Pediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
Ananthanarayanan KasinathanDepartment of Pediatric Neurology, Rainbow Children's Hospital, Chennai, Tamil Nadu, India.
Prateek Kumar PandaDepartment of Pediatrics, Pediatric Neurology Division and Evidence Synthesis Unit, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesMultifocal motor neuropathy (MMN) is an uncommon chronic autoimmune disorder in adults. Several randomized and non-randomized studies with small sample sizes have shown promising results with subcutaneous immunoglobulin (SCIg) in MMN patients who have a stable disease course with intravenous immunoglobulin (IVIg). This systematic review aimed to compare the efficacy of SCIg and IVIg treatment in MMN patients in terms of changes in muscle power, grip strength, motor function, disability, quality of life, as well as adverse effects.

methodsRandom- or fixed-effect model was used, as appropriate, to determine the pooled weighted estimates for outcome variables, depending on the degree of heterogeneity. A total of 11 publications from nine studies (110 patients, mean age 54.3 ± 3.4 years, 57% males, duration of illness 9.7 ± 2.4 years) were included in the review.

resultsChanges in the Medical Research Council sum score (MRC-SS), grip strength, dexterity, and disability due to neuropathy following IVIg and SCIg administration were comparable ( P = 0.30, I ² = 9%; P = 0.51, I ² = 0%; P = 0.45, I ² = 0%; and P = 0.57, I ² = 0%, respectively). Changes in health-related quality of life were numerically better with SCIg, although the difference did not reach statistical significance ( P = 0.17, I ² = 72%,). Over the long term, there was a trend toward fewer disease fluctuations compared to IVIg ( P = 0.43), and the efficacy comparable to IVIg was maintained in terms of muscle strength, disability, and quality of life parameters ( P = 0.83, 0.85, and 0.59, respectively). The incidence of moderate to severe systemic adverse effects was significantly lower with SCIg infusion compared to previous years when patients received IVIg ( P = 0.03).

conclusionsSCIg can be considered an acceptable alternative to IVIg in patients with MMN, with a better safety profile.

Indexed as

autoimmune neuropathychronic neuropathyimmunoglobulinsMultifocal motor neuropathyneuromuscular disease

Identifiers

PMID40265739
PMCPMC12393844

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