Evidence map›Paper›PMID 30410027›Full record

ArticleNature communications2018

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.

Julius Gudmundsson, Jon K Sigurdsson, Lilja Stefansdottir, Bjarni A Agnarsson, Helgi J Isaksson, Olafur A Stefansson, Sigurjon A Gudjonsson, Daniel F Gudbjartsson, Gisli Masson, Michael L Frigge and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 6 pooled it
4.6field-weighted citation impact, top 5% 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, 6 syntheses or guidelines pooled it, 80 citations in OpenAlex.

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  19. Changes inBiomedicines · 2024
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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

28 authors at 4 institutions in 3 countries.

Julius GudmundssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland. julius.gudmundsson@decode.is.
Jon K SigurdssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Lilja StefansdottirdeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Bjarni A AgnarssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Helgi J IsakssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Olafur A StefanssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Sigurjon A GudjonssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Daniel F GudbjartssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-5222-9857
Gisli MassondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Michael L FriggedeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Simon N StaceydeCODE genetics/AMGEN, 101, Reykjavik, Iceland.ORCID http://orcid.org/0000-0002-4732-7380
Patrick SulemdeCODE genetics/AMGEN, 101, Reykjavik, Iceland.ORCID http://orcid.org/0000-0001-7123-6123
Gisli H HalldorssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.ORCID http://orcid.org/0000-0001-7067-9862
Vinicius TragantedeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Hilma HolmdeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Gudmundur I EyjolfssonThe Clinical Laboratory in Mjodd, 109, Reykjavik, Iceland.
Olof SigurdardottirDepartment of Clinical Biochemistry, Akureyri Hospital, 600, Akureyri, Iceland.
Isleifur OlafssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Thorvaldur JonssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Eirikur JonssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Rosa B BarkardottirLaboratory of Cell Biology, Department of Pathology, Landspitali University Hospital, 101, Reykjavik, Iceland.
Rafn HilmarssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Folkert W AsselbergsDepartment of Cardiology, Division Heart & Lungs, University Medical Center Utrecht, University of Utrecht, 3584 CX, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-1692-8669
Gudmundur GeirssonLandspitali-University Hospital, 101, Reykjavik, Iceland.
Unnur ThorsteinsdottirdeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Thorunn RafnardeCODE genetics/AMGEN, 101, Reykjavik, Iceland.ORCID http://orcid.org/0000-0003-0491-7046
Gudmar ThorleifssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland.
Kari StefanssondeCODE genetics/AMGEN, 101, Reykjavik, Iceland. kstefans@decode.is.ORCID http://orcid.org/0000-0003-1676-864X
deCODE Genetics (Iceland) · ISReykjavík University · ISAkureyri Hospital · ISUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Benign prostatic hyperplasia and associated lower urinary tract symptoms (BPH/LUTS) are common conditions affecting the majority of elderly males. Here we report the results of a genome-wide association study of symptomatic BPH/LUTS in 20,621 patients and 280,541 controls of European ancestry, from Iceland and the UK. We discovered 23 genome-wide significant variants, located at 14 loci. There is little or no overlap between the BPH/LUTS variants and published prostate cancer risk variants. However, 15 of the variants reported here also associate with serum levels of prostate specific antigen (PSA) (at a Bonferroni corrected P < 0.0022). Furthermore, there is a strong genetic correlation, r

Indexed as

Genome-Wide Association StudyAcetylationAgedComputational BiologyGenetic Predisposition to DiseaseHistonesHumansIcelandLower Urinary Tract SymptomsLysineMaleMeta-Analysis as TopicMultifactorial InheritanceMutationPhenotypeProstate-Specific AntigenHistonesLysineProstate-Specific Antigen

Identifiers

PMID30410027
PMCPMC6224563
OpenAlexW2898103663

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.