Evidence map›Paper›PMID 40021967›Full record

ArticleBMC medical research methodology2025

Handling of missing component information for common composite score outcomes used in axial spondyloarthritis research when complete-case analysis is unbiased.

Christos Polysopoulos, Stylianos Georgiadis, Lykke Midtbøll Ørnbjerg, Almut Scherer, Daniela Di Giuseppe, Merete Lund Hetland, Michael John Nissen, Gareth T Jones, Bente Glintborg, Anne Gitte Loft and 18 more

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Christos PolysopoulosStatistics Group, Swiss Clinical Quality Management (SCQM) Foundation, Aargauerstrasse 250, Zurich, 8048, Switzerland.
Stylianos GeorgiadisCopenhagen Centre for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
Lykke Midtbøll ØrnbjergCopenhagen Centre for Arthritis Research (COPECARE), Centre for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
Almut SchererStatistics Group, Swiss Clinical Quality Management (SCQM) Foundation, Aargauerstrasse 250, Zurich, 8048, Switzerland.
Daniela Di GiuseppeDepartment of Medicine Solna, Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden.
Merete Lund HetlandCopenhagen Centre for Arthritis Research (COPECARE) and the DANBIO Registry, Centre for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
Michael John NissenDepartment of Rheumatology, Geneva University Hospital, Geneva, Switzerland.
Gareth T JonesAberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, UK.
Bente GlintborgCopenhagen Centre for Arthritis Research (COPECARE) and the DANBIO Registry, Centre for Rheumatology and Spine Diseases, Centre for Head and Orthopaedics, Rigshospitalet, Glostrup, Denmark.
Anne Gitte LoftDepartment of Rheumatology, Aarhus University Hospital, Aarhus, Denmark.
Johan Karlsson WallmanDepartment of Clinical Sciences Lund, Rheumatology, Skåne University Hospital, Lund University, Lund, Sweden.
Karel PavelkaInstitute of Rheumatology, Prague, Czech Republic.
Jakub ZávadaInstitute of Rheumatology, Prague, Czech Republic.
Ayten YaziciDivision of Rheumatology, Department of Internal Medicine, School of Medicine, Kocaeli University, Kocaeli, Turkey.
Maria José SantosSociedade Portuguesa de Reumatologia, Reuma.Pt, Lisbon, Portugal.
Adrian CiureaDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Burkhard MöllerDepartment Rheumatology and Immunology, Inselspital - University Hospital Bern, Bern, Switzerland.
Brigitte MichelsenCenter for Treatment of Rheumatic and Musculoskeletal Diseases (REMEDY), Diakonhjemmet Hospital, Oslo, Norway.
Pawel MielnikSection for Rheumatology, Department for Neurology, Rheumatology and Physical Medicine, Helse Førde, Førde, Norway.
Johanna HuhtakangasDepartment of Rheumatology, Kuopio University Hospital, Kuopio, Finland.
Heikki RelasRheumatology, Inflammation Center, Helsinki University Hospital and University of Helsink, Helsinki, Finland.
Katja Perdan PirkmajerFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Ziga RotarFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Ross MacDonaldAberdeen Centre for Arthritis and Musculoskeletal Health (Epidemiology Group), University of Aberdeen, Aberdeen, UK.
Bjorn GudbjornssonFaculty of Medicine, University of Iceland, Reykjavik, Iceland.
Irene van der Horst-BruinsmaRheumatology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Marleen van de SandeAmsterdam UMC, Department of Rheumatology & Clinical Immunology and Department of Experimental Immunology, Amsterdam Institute for Infection & Immunity, University of Amsterdam, Amsterdam, The Netherlands.
Myriam RiekStatistics Group, Swiss Clinical Quality Management (SCQM) Foundation, Aargauerstrasse 250, Zurich, 8048, Switzerland. myriam.riek@scqm.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObservational data on composite scores often comes with missing component information. When a complete-case (CC) analysis of composite scores is unbiased, preferable approaches of dealing with missing component information should also be unbiased and provide a more precise estimate. We assessed the performance of several methods compared to CC analysis in estimating the means of common composite scores used in axial spondyloarthritis research.

methodsIndividual mean imputation (IMI), the modified formula method (MF), overall mean imputation (OMI), and multiple imputation of missing component values (MI) were assessed either analytically or by means of simulations from available data collected across Europe. Their performance in estimating the means of the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), the Bath Ankylosing Spondylitis Functional Index (BASFI), and the Ankylosing Spondylitis Disease Activity Score based on C-reactive protein (ASDAS-CRP) in cases where component information was set missing completely at random was compared to the CC approach based on bias, variance, and coverage.

resultsLike the MF method, IMI uses a modified formula for observations with missing components resulting in modified composite scores. In the case of an unbiased CC approach, these two methods yielded representative samples of the distribution arising from a mixture of the original and modified composite scores, which, however, could not be considered the same as the distribution of the original score. The IMI and MF method are, thus, intrinsically biased. OMI provided an unbiased mean but displayed a complex dependence structure among observations that, if not accounted for, resulted in severe coverage issues. MI improved precision compared to CC and gave unbiased means and proper coverage as long as the extent of missingness was not too large.

conclusionsMI of missing component values was the only method found successful in retaining CC's unbiasedness and in providing increased precision for estimating the means of BASDAI, BASFI, and ASDAS-CRP. However, since MI is susceptible to incorrect implementation and its performance may become questionable with increasing missingness, we consider the implementation of an error-free CC approach a valid and valuable option.

trial registrationNot applicable as study uses data from patient registries.

Indexed as

Axial SpondyloarthritisBiasC-Reactive ProteinData Interpretation, StatisticalEuropeHumansResearch DesignSeverity of Illness IndexC-Reactive ProteinAxial spondyloarthritisComplete-case analysisComposite scoreMissing componentsMultiple imputation

Identifiers

PMID40021967
PMCPMC11869558

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.