Evidence map›Paper›PMID 26785608›Full record

ArticleArthritis research & therapy2016

Perinatal characteristics, older siblings, and risk of ankylosing spondylitis: a case-control study based on national registers.

Ulf Lindström, Helena Forsblad-d'Elia, Johan Askling, Lars Erik Kristensen, Elisabeth Lie, Sofia Exarchou, Lennart Jacobsson

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Epidemiology of axial spondyloarthritis: an update.Current opinion in rheumatology · 2018
    Review
  5. 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

7 authors.

Ulf LindströmDepartment of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, 405 30, Gothenburg, Sweden. ulf.lindstrom@gu.se.
Helena Forsblad-d'EliaInstitution of Public Health and Clinical Medicine/Rheumatology, Umeå University, Lasarettsgatan 7, 901 87, Umeå, Sweden. helena.forsblad.delia@umu.se.
Johan AsklingRheumatology Unit and Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Nobels väg 5, Solna, 171 76, Stockholm, Sweden. johan.askling@ki.se.
Lars Erik KristensenThe Parker Institute, Department of Rheumatology, Frederiksberg and Bispebjerg Hospital, Nordre Fasanvej 57, 2000, Frederiksberg, Denmark. larserik_kristensen@yahoo.com.
Elisabeth LieDepartment of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, 405 30, Gothenburg, Sweden. elisabeth_lie@yahoo.no.
Sofia ExarchouSection of Rheumatology, Department of Clinical Sciences, Lund University, Barngatan 2B, 221 85, Lund, Sweden. sofiaexar@hotmail.com.
Lennart JacobssonDepartment of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Guldhedsgatan 10A, 405 30, Gothenburg, Sweden. lennart.jacobsson@gu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe effect of circumstances and exposures early in life on the risk of developing ankylosing spondylitis (AS) is largely unknown. The purpose of this study was to determine whether perinatal characteristics predict development of AS.

methodsAS cases (n = 1960; 59 % men) were defined as listed with a diagnosis of AS at least once in the Swedish National Patient Register and registered in the Swedish Medical Birth Register (born ≥1973). Population controls were retrieved from the Swedish Population Register (n = 8378; mean 4.3 controls/case), matched on birth year, sex and county. Odds ratios (OR) for developing AS were determined through conditional logistic regression, with regard to: birth weight, birth order, season of birth, maternal age, gestational length, size for gestational age, type of birth, mode of delivery, congenital malformations, mothers' country of birth, mothers' civil status and size of delivery unit.

resultsIn the univariate analyses statistically significant increases in risk for developing AS were observed for having older siblings (OR 1.18; 95 % Cl 1.06-1.30). No association was observed for the remainder of analysed exposures, although there was a weak association with birth weight below 3000 g (OR 1.19; 95 % CI 1.04-1.37), though not for "low birth weight" <2500 g (OR 0.90; 95 % CI 0.70-1.16). The increase in risk associated with having older siblings was consistent in a multivariate analysis adjusting for possible confounders (OR 1.23; 95 % Cl 1.09-1.39). The direction and magnitude of the point estimates were also consistent in several sensitivity analyses and when stratifying by sex.

conclusionsHaving older siblings was associated with an increased risk for developing AS. These results need to be repeated and confirmed in other cohorts.

Indexed as

Perinatal CareRegistriesSiblingsAdultBirth WeightCase-Control StudiesFemaleHumansMalePregnancyRisk FactorsSeasonsSpondylitis, AnkylosingSwedenYoung Adult

Identifiers

PMID26785608
PMCPMC4718040

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.