Evidence map›Paper›PMID 19411462›Full record

ArticleThe Journal of bone and joint surgery. American volume2009

Evidence for an inherited predisposition contributing to the risk for rotator cuff disease.

Robert Z Tashjian, James M Farnham, Frederick S Albright, Craig C Teerlink, Lisa A Cannon-Albright

Open access · greenAbstract read
In one paragraph

Article in The Journal of bone and joint surgery. American volume, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 4% of its field
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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it, 111 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Shoulder and genetics: what orthopedic surgeons need to know.JSES reviews, reports, and techniques · 2026
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  17. Genetic Aspects in Shoulder Disorders.Revista brasileira de ortopedia · 2020
    Article
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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

5 authors at 1 institution in 1 country.

Robert Z TashjianUniversity of Utah Orthopaedic Center, Salt Lake City, UT 84108, USA. Robert.Tashjian@hsc.utah.edu
James M Farnham
Frederick S Albright
Craig C Teerlink
Lisa A Cannon-Albright
University of Utah · US

Funding

Analysis of the Familial Component to Disease in a Biomedical Resource w/Link...R01LM009331 · NLM · UNIVERSITY OF UTAH · PI ALBRIGHT, LISA CANNON · 2007 to 2010
$1.6M
NLM NIH HHS R01 LM009331
6 · The paper itself

Abstract

backgroundA genetic predisposition has been suggested to contribute to the risk for development of rotator cuff disease on the basis of observed family clusters of close relatives. We used a population-based resource combining genealogical data for Utah with clinical diagnosis data from a large Utah hospital to test the hypothesis of excess familial clustering for rotator cuff disease.

methodsThe Utah Population Database contains combined health and genealogical data on over two million Utah residents. Current Procedural Terminology, Fourth Revision, codes (29827, 23412, 23410, and 23420) and International Classification of Diseases, Ninth Revision, codes (726.1, 727.61, and 840.4) entered in patient records were used to identify patients with rotator cuff disease. We tested the hypothesis of excess familial clustering using two well-established methods (the Genealogical Index of Familiality test and the estimation of relative risks in relatives) in the overall study group (3091 patients) and a subgroup of the study group diagnosed before the age of forty years (652 patients).

resultsThe Genealogical Index of Familiality test in patients diagnosed before the age of forty years showed significant excess relatedness for individuals with rotator cuff disease in close and distant relationships (as distant as third cousins) (p = 0.001). The relative risk of rotator cuff disease in the relatives of patients diagnosed before the age of forty years was significantly elevated for second degree (relative risk = 3.66, p = 0.0076) and third degree (relative risk = 1.81, p = 0.0479) relatives.

conclusionsWe analyzed a set of patients with diagnosed rotator cuff disease and a known genealogy to describe the familial clustering of affected individuals. The observations of significant excess relatedness of patients and the significantly elevated risks to both close and distant relatives of patients strongly support a heritable predisposition to rotator cuff disease.

Indexed as

Rotator CuffAdultFamilyGenealogy and HeraldryGenetic Predisposition to DiseaseHumansMuscular DiseasesUtah

Identifiers

PMID19411462
PMCPMC2674244
OpenAlexW2034981739

What OpenQuestion holds

Textmetadata
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.