Evidence map›Paper›PMID 34047840›Full record

ArticleHuman genetics2021

Novel loci and Mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys.

Lucas Vicuña, Tomás Norambuena, José Patricio Miranda, Ana Pereira, Veronica Mericq, Linda Ongaro, Francesco Montinaro, José L Santos, Susana Eyheramendy

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Lucas VicuñaFaculty of Engineering and Sciences, Universidad Adolfo Ibáñez, Peñalolén, Santiago, Chile.
Tomás NorambuenaFaculty of Engineering and Sciences, Universidad Adolfo Ibáñez, Peñalolén, Santiago, Chile.
José Patricio MirandaFaculty of Engineering and Sciences, Universidad Adolfo Ibáñez, Peñalolén, Santiago, Chile.
Ana PereiraInstitute of Nutrition and Food Technology, University of Chile, Santiago, Chile.
Veronica MericqInstitute of Maternal and Child Research, Faculty of Medicine, University of Chile, Santiago, Chile.
Linda OngaroEstonian Biocentre, Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
Francesco MontinaroEstonian Biocentre, Institute of Genomics, University of Tartu, Riia 23b, 51010, Tartu, Estonia.
José L SantosDepartment of Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Susana EyheramendyFaculty of Engineering and Sciences, Universidad Adolfo Ibáñez, Peñalolén, Santiago, Chile. susana.eyheramendy@uai.cl.ORCID http://orcid.org/0000-0003-4723-9660
Adolfo Ibáñez University · CLEstonian Biocentre · EEUniversity of Chile · CLPontificia Universidad Católica de Chile · CL

Funding

Fondo Nacional de Desarrollo Científico y Tecnológico 1200146Fondo Nacional de Desarrollo Científico y Tecnológico 150416Fondo Nacional de Desarrollo Científico y Tecnológico 160833Fondo Nacional de Desarrollo Científico y Tecnológico 3170038
6 · The paper itself

Abstract

Puberty is a complex developmental process that varies considerably among individuals and populations. Genetic factors explain a large proportion of the variability of several pubertal traits. Recent genome-wide association studies (GWAS) have identified hundreds of variants involved in traits that result from body growth, like adult height. However, they do not capture many genetic loci involved in growth changes over distinct growth phases. Further, such GWAS have been mostly performed in Europeans, but it is unknown how these findings relate to other continental populations. In this study, we analyzed the genetic basis of three pubertal traits; namely, peak height velocity (PV), age at PV (APV) and height at APV (HAPV). We analyzed a cohort of 904 admixed Chilean children and adolescents with European and Mapuche Native American ancestries. Height was measured on roughly a [Formula: see text]month basis from childhood to adolescence between 2006 and 2019. We predict that, in average, HAPV is 4.3 cm higher in European than in Mapuche adolescents (P = 0.042), and APV is 0.73 years later in European compared with Mapuche adolescents (P = 0.023). Further, by performing a GWAS on 774, 433 single-nucleotide polymorphisms, we identified a genetic signal harboring 3 linked variants significantly associated with PV in boys (P [Formula: see text]). This signal has never been associated with growth-related traits.

Indexed as

AdolescentAdolescent DevelopmentAdultAgingBody HeightChileCohort StudiesFemaleGenetic VariationGenome-Wide Association StudyHumansIndians, South AmericanMalePubertyWhite People

Identifiers

PMID34047840
PMCPMC8553699
OpenAlexW3165128431

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.