Evidence map›Paper›PMID 39741705›Full record

ArticleFrontiers in neurology2024

Association between telomere length and idiopathic normal pressure hydrocephalus: a Mendelian randomization study.

Feng Yang, Hanlin Cai, Yimeng Ren, Keru Huang, Hui Gao, Linyuan Qin, Ruihan Wang, Yongping Chen, Liangxue Zhou, Dong Zhou and 1 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 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
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

  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

11 authors.

Feng Yang *Department of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Hanlin Cai *Department of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Yimeng RenDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Keru HuangDepartment of Neurosurgery, West China Hospital of Sichuan University, Chengdu, China.
Hui GaoDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Linyuan QinDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Ruihan WangDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Yongping ChenDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Liangxue ZhouDepartment of Neurosurgery, West China Hospital of Sichuan University, Chengdu, China.
Dong ZhouDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Qin ChenDepartment of Neurology, West China Hospital of Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Idiopathic normal pressure hydrocephalus (iNPH) is highly prevalent among elderly individuals, and there is a strong correlation between telomere length and biological aging. However, there is limited evidence to elucidate the relationship between telomere length and iNPH. This study aimed to investigate the associations between telomere length and iNPH using the Mendelian randomization (MR) method. Methods: The genetic variants of telomere length were obtained from 472,174 UK Biobank individuals. Summary level data of iNPH were acquired from 218,365 individuals of the FinnGen consortium. Five MR estimation methods, including inverse-variance weighting (IVW), MR-Egger regression, weighted median, weighted mode and simple mode, were used for causal inference. Comprehensive sensitivity analyses were conducted to test the robustness of the results. In addition, multivariable MR was further implemented to identify potential mechanisms in the causal pathway from telomere length to iNPH. Results: Genetically determined longer telomere length was significantly associated with decreased risk of iNPH (OR = 0.44, 95% CI 0.24-0.80; Conclusion: Our MR study revealed a strong negative correlation of telomere length with iNPH. The causal relationship might be driven by several vascular risk factors.

Indexed as

causal relationshipidiopathic normal pressure hydrocephalusMendelian randomizationtelomere lengthvascular risk factors

Identifiers

PMID39741705
PMCPMC11686450

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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.