Evidence map›Paper›PMID 42185559›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2026

Clinical, demographic, and pharmacological predictors of medication adherence to disease-modifying therapies in multiple sclerosis: a multidimensional analysis of merged survey and claims data.

Ahkash Thavarajasingam, Lara Marleen Fricke, Christian Krauth

Abstract read
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ahkash ThavarajasingamHannover Medical School, Institute for Epidemiology, Social Medicine and Health Systems Research, Hannover, Germany. thavarajasingam.ahkash@mh-hannover.de.
Lara Marleen FrickeHannover Medical School, Institute for Epidemiology, Social Medicine and Health Systems Research, Hannover, Germany.
Christian KrauthHannover Medical School, Institute for Epidemiology, Social Medicine and Health Systems Research, Hannover, Germany.

Funding

German Federal Joint Committee's Innovation Fund 01VSF19046
6 · The paper itself

Abstract

Sustained adherence to disease-modifying therapies (DMTs) is essential for achieving therapeutic benefit in multiple sclerosis (MS). Despite the availability of effective agents, adherence has been reported as variable and often suboptimal in German cohorts, and the relative influence of clinical, demographic, and pharmacological factors remains insufficiently characterised. This study therefore examined predictors of objective adherence to DMTs in people with MS and the association between subjective and objective adherence. We analysed 795 people with MS (PwMS) receiving oral, subcutaneous, or intramuscular DMTs between October 2020 and September 2021. Objective adherence was measured using the Medication Possession Ratio (MPR), and subjective adherence using a visual analogue scale. Permutation-based multivariable analyses (PERMANOVA) were used to examine associations between predefined predictors and MPR. Objective adherence averaged 88.4% (SD 18.0). Subjective adherence was substantially higher, averaging 95.9% (SD 11.6; median 100%), with a pronounced ceiling effect. Therapy-related characteristics were the only consistent predictors of adherence. Oral agents and intramuscular interferon beta-1a achieved comparable adherence (p = 0.90), both exceeding that of subcutaneous therapies (both p < 0.001); within interferons, intramuscular exceeded subcutaneous administration (p = 0.002). Across active substances, glatiramer acetate showed the lowest adherence and teriflunomide, sphingosine-1-phosphate (S1P) receptor modulators, and dimethyl fumarate the highest (all p < 0.001 vs. glatiramer acetate). Demographic, including socioeconomic, and clinical characteristics, comprising age, sex, income, education, employment, MS subtype, disease duration, and disease activity, showed no measurable association with adherence. Subjective and objective adherence correlated only weakly (Spearman's ρ = 0.10; p = 0.005). Adherence patterns in MS were largely shaped by pharmacological and administration-related factors rather than by patient demographics or clinical profile. The weak correlation between subjective and objective measures supports complementing patient report with objective adherence indicators in routine care.

Indexed as

Drug MonitoringImmunologic FactorsImmunosuppressive AgentsMedication AdherenceMultiple SclerosisAdministration, OralAdultCrotonatesDimethyl FumarateFemaleFingolimod HydrochlorideGermanyHumansHydroxybutyratesInjections, IntramuscularInjections, SubcutaneousCrotonatesDimethyl FumarateFingolimod HydrochlorideHydroxybutyratesImmunologic FactorsImmunosuppressive AgentsInterferon beta-1aNitrilesteriflunomideToluidinesDisease-modifying therapiesMedication adherenceMedication possession ratioMultiple sclerosis

Identifiers

PMID42185559
PMCPMC13503424

What Socratic holds

Textmetadata
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Registered trials

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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 Socratic graph.