Evidence map›Paper›PMID 38451181›Full record

ArticleAging2024

Genetically determined telomere length as a risk factor for hematological malignancies: evidence from Mendelian randomization analysis.

Tian Fang, Zhihao Zhang, Kexing Ren, Liqun Zou

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Tian FangDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Zhihao ZhangDepartment of Breast Center, West China Hospital, Sichuan University, Chengdu, China.
Kexing RenDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Liqun ZouDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver the past years, the exact correlation between telomere length and hematological malignancies was still not fully understood.

methodsWe performed a two-sample Mendelian randomization study to investigate the causal relationship between telomere length and hematological malignancies. We selected genetic instruments associated with telomere length. The genetic associations for lymphoid and hematopoietic malignant neoplasms were obtained from the most recent publicly accessible FinnGen study R9 data. Inverse variant weighted (IVW) analysis was adopted as the primary method, and we also performed the weighted-median method and the MR-Egger, and MRPRESSO methods as sensitive analysis.

resultsSignificant associations have been observed between telomere length and primary lymphoid (IVW: OR = 1.52,

conclusionThis MR study found a significant association between telomere length and a wide range of hematopoietic malignancies. But no substantial impact of lymphoma and hematopoietic malignancies on telomere length has been detected.

Indexed as

Hematologic NeoplasmsHodgkin DiseaseGenome-Wide Association StudyHumansMendelian Randomization AnalysisRisk FactorsTelomerecausal relationshiphematopoietic malignancieslymphomaMendelian randomizationtelomere length

Identifiers

PMID38451181
PMCPMC10968690
OpenAlexW4392508909

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.