Evidence map›Paper›PMID 32527150›Full record

ArticleCirculation. Genomic and precision medicine2020

Genetic Risk Scores for Complex Disease Traits in Youth.

Tian Xie, Bin Wang, Ilja M Nolte, Peter J van der Most, Albertine J Oldehinkel, Catharina A Hartman, Harold Snieder

Open access · hybridAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.2field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Tian XieDepartment of Epidemiology (T.X., B.W., I.M.N., P.J.v.d.M., H.S.), University of Groningen, University Medical Center Groningen, the Netherlands.
Bin WangDepartment of Epidemiology (T.X., B.W., I.M.N., P.J.v.d.M., H.S.), University of Groningen, University Medical Center Groningen, the Netherlands.
Ilja M NolteDepartment of Epidemiology (T.X., B.W., I.M.N., P.J.v.d.M., H.S.), University of Groningen, University Medical Center Groningen, the Netherlands.
Peter J van der MostDepartment of Epidemiology (T.X., B.W., I.M.N., P.J.v.d.M., H.S.), University of Groningen, University Medical Center Groningen, the Netherlands.
Albertine J OldehinkelDepartment of Psychiatry (A.J.O., C.A.H.), University of Groningen, University Medical Center Groningen, the Netherlands.
Catharina A HartmanDepartment of Psychiatry (A.J.O., C.A.H.), University of Groningen, University Medical Center Groningen, the Netherlands.
Harold SniederDepartment of Epidemiology (T.X., B.W., I.M.N., P.J.v.d.M., H.S.), University of Groningen, University Medical Center Groningen, the Netherlands.
University Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor most disease-related traits the magnitude of the contribution of genetic factors in adolescents remains unclear.

methodsTwenty continuous traits related to anthropometry, cardiovascular and renal function, metabolism, and inflammation were selected from the ongoing prospective Tracking Adolescents' Individual Lives Survey cohort in the Netherlands with measurements of up to 5 waves from age 11 to 22 years (n=1354, 47.6% males) and all traits available at the third wave (mean age [SD]=16.22 [0.66]). For each trait, unweighted and weighted genetic risk scores (GRSs) were generated based on significantly associated single nucleotide polymorphisms identified from literature. The variance explained by the GRSs in adolescents were estimated by linear regression after adjustment for covariates.

resultsExcept for ALT (alanine transaminase), all GRSs were significantly associated with their traits. The trait variance explained by the GRSs was highest for lipoprotein[a] (39.59%) and varied between 0.09% (ALT) and 18.49% (LDL [low-density lipoprotein]) for the other traits. For most traits, the variances explained in adolescents were comparable with or slightly smaller than those in adults. Significant increases of trait levels (except ALT) and increased risks for overweight/obesity (odds ratio, 6.41 [95% CI, 2.95-15.56]) and hypertension (odds ratio, 2.86 [95% CI, 1.39-6.17]) were found in individuals in the top GRS decile compared with those at the bottom decile.

conclusionsVariances explained by adult-based GRSs for disease-related traits in adolescents, although still relatively modest, were comparable with or slightly smaller than in adults offering promise for improved risk prediction at early ages.

Indexed as

Genetic Predisposition to DiseaseAdolescentAlanine TransaminaseBody Mass IndexChildFemaleGenome-Wide Association StudyHumansHypertensionLinkage DisequilibriumLipoprotein(a)Lipoproteins, LDLMaleMultifactorial InheritanceNetherlandsObesityAlanine TransaminaseLipoprotein(a)Lipoproteins, LDLadolescentblood pressurebody mass indexgenetic predisposition to diseasegenetic variation

Identifiers

PMID32527150
PMCPMC7439939
OpenAlexW3035273325

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.