Evidence map›Paper›PMID 35681050›Full record

ArticleCommunications biology2022

Genetic, parental and lifestyle factors influence telomere length.

Sergio Andreu-Sánchez, Geraldine Aubert, Aida Ripoll-Cladellas, Sandra Henkelman, Daria V Zhernakova, Trishla Sinha, Alexander Kurilshikov, Maria Carmen Cenit, Marc Jan Bonder, Lude Franke and 6 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 3 pooled it
8.0field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 3 syntheses or guidelines pooled it, 73 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

16 authors at 5 institutions in 5 countries.

Sergio Andreu-Sánchez *Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. s.andreu.sanchez@umcg.nl.ORCID 0000-0002-3503-9971
Geraldine Aubert *Terry Fox Laboratory, British Columbia Cancer Research Center, Vancouver, BC, Canada.
Aida Ripoll-Cladellas *Life Sciences Department, Barcelona Supercomputing Center, 08034, Barcelona, Catalonia, Spain.ORCID 0000-0001-7317-3736
Sandra Henkelman *European Research Institute for the Biology of Ageing, University of Groningen, Groningen, the Netherlands.
Daria V ZhernakovaDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Trishla SinhaDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-0992-7983
Alexander KurilshikovDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0003-2541-5627
Maria Carmen CenitDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Marc Jan BonderDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Lude FrankeDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-5159-8802
Cisca WijmengaDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0002-5635-1614
Jingyuan FuDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Monique G P van der WijstDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
Marta MeléLife Sciences Department, Barcelona Supercomputing Center, 08034, Barcelona, Catalonia, Spain.
Peter LansdorpTerry Fox Laboratory, British Columbia Cancer Research Center, Vancouver, BC, Canada. plansdor@bccrc.ca.ORCID 0000-0001-7435-1071
Alexandra ZhernakovaDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands. a.zhernakova@umcg.nl.ORCID 0000-0002-4574-0841
University Medical Center Groningen · NLBarcelona Supercomputing Center · ESTerry Fox Research Institute · CAUniversity of British Columbia · CAUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The average length of telomere repeats (TL) declines with age and is considered to be a marker of biological ageing. Here, we measured TL in six blood cell types from 1046 individuals using the clinically validated Flow-FISH method. We identified remarkable cell-type-specific variations in TL. Host genetics, environmental, parental and intrinsic factors such as sex, parental age, and smoking are associated to variations in TL. By analysing the genome-wide methylation patterns, we identified that the association of maternal, but not paternal, age to TL is mediated by epigenetics. Single-cell RNA-sequencing data for 62 participants revealed differential gene expression in T-cells. Genes negatively associated with TL were enriched for pathways related to translation and nonsense-mediated decay. Altogether, this study addresses cell-type-specific differences in telomere biology and its relation to cell-type-specific gene expression and highlights how perinatal factors play a role in determining TL, on top of genetics and lifestyle.

Indexed as

AgingTelomereEpigenesis, GeneticFemaleHumansLife StyleParentsPregnancy

Identifiers

PMID35681050
PMCPMC9184499
OpenAlexW4281759862

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.