# Robust evidence supports a causal link between higher birthweight and longer telomere length: a mendelian randomization study

**Authors:** Zhuoya Zhang, Jiale Zhang, Kaiqi Zhang, Xiaolei Ge, Xu Zhai

PMC · DOI: 10.3389/fgene.2024.1264028 · Frontiers in Genetics · 2024-06-21

## TL;DR

This study finds a causal link between higher birth weight and longer telomere length using genetic data.

## Contribution

The study provides robust causal evidence using Mendelian Randomization to link birth weight and telomere length.

## Key findings

- Genetically predicted higher birth weight is associated with longer telomere length.
- Inverse variance weighted analysis confirmed a significant causal relationship (Beta = 0.048; p < 0.001).

## Abstract

Observational studies have suggested a potential relationship between birthweight and telomere length. However, the causal link between these two parameters remains undefined. In this study, we use Mendelian Randomization (MR). This method employs genetic variants as instrumental variables, to explore the existence of causal associations and elucidate the causal relationship between birth weight and telomere length.

We used 35 single nucleotide polymorphisms (SNPs) as instrumental variables for birth weight. These SNPs were identified from a meta-analysis involving 153,781 individuals. Furthermore, we obtained summary statistics for telomere length from a study conducted on 472,174 United Kingdom Biobank participants. To evaluate the causal estimates, we applied the random effect inverse variance weighted method (IVW) and several other MR methods, such as MR-Egger, weighted median, and MR-PRESSO, to verify the reliability of our findings.

Our analysis supports a significant causal relationship between genetically predicted birth weight and telomer3e length. The inverse variance weighted analysis results for birth weight (Beta = 0.048; 95%CI = 0.023 to 0.073; p < 0.001) corroborate this association.

Our study provides robust evidence supporting a causal link between higher birth weight and longer telomere length.

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** weight gain (MESH:D015430), MR (MESH:C562757), cancer (MESH:D009369), inflammation (MESH:D007249), cardiovascular disease (MESH:D002318), overweight (MESH:D050177), birthweight abnormality (MESH:D001724), type 2 diabetes (MESH:D003924), inflammatory cytokines (MESH:D000080424), age-related disease (MESH:D010024)

## Full text

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## Figures

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC11224456/full.md

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Source: https://tomesphere.com/paper/PMC11224456