» Articles » PMID: 38027166

Causal Relationship Between Breakfast Skipping and Bone Mineral Density: a Two-sample Mendelian Randomized Study

Overview
Specialty Endocrinology
Date 2023 Nov 29
PMID 38027166
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: To explore the causal association between breakfast skipping and bone mineral density (BMD) through two-sample Mendelian randomisation (MR) analysis.

Methods: A two-sample MR approach was adopted to explore the causal relationship of breakfast skipping with BMDs (across three skeletal sites and five age groups). Publicly available genome-wide association study summary data were used for MR analysis. We used five methods to estimate the causal associations between breakfast skipping and BMDs: inverse-variance weighting (IVW), MR-Egger, weighted median, simple mode, and weighted mode. IVW was used for the main analysis and the remaining four methods were used as supplementary analyses. The heterogeneity of the MR results was determined using IVW and MR-Egger methods. The pleiotropy of the MR results was determined using MR-Egger intercept. Furthermore, a leave-one-out test was performed to determine whether the MR results were affected by a single nucleotide polymorphism.

Results: With the IVW method, we did not find any causal relationship between breakfast skipping and forearm, femoral neck, and lumbar spine BMD. Subsequently, when we included BMD data stratified by five different age groups in the analysis, the results showed that there was no apparent causal effect between breakfast skipping and age-stratified BMD. This finding was supported by all four supplementary methods (P > 0.05 for all methods). No heterogeneity or horizontal pleiotropy was detected in any of the analyses (P > 0.05). The leave-one-out tests conducted in the analyses did not identify any single nucleotide polymorphism that could have influenced the MR results, indicating the reliability of our findings.

Conclusion: No causal effect was found between breakfast skipping and BMD (across three skeletal sites and five age groups).

Citing Articles

Exploring the Association Between Human Blood Metabolites and Autism Spectrum Disorder Risk: A Bidirectional Mendelian Randomization Study.

Li W, Ma S, Tian Y Health Sci Rep. 2025; 8(3):e70528.

PMID: 40041792 PMC: 11875788. DOI: 10.1002/hsr2.70528.


Causal relationship between breakfast skipping and myocardial infarction: Two-sample Mendelian randomization.

Guo Y, Lv L, Gao H, Feng R, Guo M Medicine (Baltimore). 2024; 103(30):e38895.

PMID: 39058860 PMC: 11272345. DOI: 10.1097/MD.0000000000038895.


Association between the atherogenic index of plasma and bone mineral density among adult women: NHANES (2011-2018).

He Q, Chen B, Liang F, Zhang Z Front Endocrinol (Lausanne). 2024; 15:1363889.

PMID: 38836228 PMC: 11148244. DOI: 10.3389/fendo.2024.1363889.

References
1.
Milne R, Kuchenbaecker K, Michailidou K, Beesley J, Kar S, Lindstrom S . Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Nat Genet. 2017; 49(12):1767-1778. PMC: 5808456. DOI: 10.1038/ng.3785. View

2.
Burgess S, Thompson S . Interpreting findings from Mendelian randomization using the MR-Egger method. Eur J Epidemiol. 2017; 32(5):377-389. PMC: 5506233. DOI: 10.1007/s10654-017-0255-x. View

3.
Hartwig F, Davey Smith G, Bowden J . Robust inference in summary data Mendelian randomization via the zero modal pleiotropy assumption. Int J Epidemiol. 2017; 46(6):1985-1998. PMC: 5837715. DOI: 10.1093/ije/dyx102. View

4.
Davey Smith G, Hemani G . Mendelian randomization: genetic anchors for causal inference in epidemiological studies. Hum Mol Genet. 2014; 23(R1):R89-98. PMC: 4170722. DOI: 10.1093/hmg/ddu328. View

5.
Ishimoto Y, Yoshida M, Nagata K, Yamada H, Hashizume H, Yoshimura N . Consuming breakfast and exercising longer during high school increases bone mineral density in young adult men. J Bone Miner Metab. 2012; 31(3):329-36. DOI: 10.1007/s00774-012-0415-8. View