File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.3390/genes16050564
- Scopus: eid_2-s2.0-105006728757
- PMID: 40428387
Supplementary
- Citations:
- Appears in Collections:
Article: Body Mass Index as an Example of a Negative Confounder: Evidence and Solutions
| Title | Body Mass Index as an Example of a Negative Confounder: Evidence and Solutions |
|---|---|
| Authors | |
| Keywords | body mass index Mendelian randomization negative confounding physiological attributes |
| Issue Date | 10-May-2025 |
| Publisher | MDPI |
| Citation | Genes, 2025, v. 16, n. 5 How to Cite? |
| Abstract | Background: Adequate control for confounding is key to many observational study designs. Confounders are often identified based on subject matter knowledge from empirical investigations. Negative confounders, which typically generate type 2 error, i.e., false nulls, can be elusive. Such confounders can be identified comprehensively by using Mendelian randomization (MR) to search the wealth of publicly available data systematically. Here, to demonstrate the concept, we examined whether a common positive confounder, body mass index (BMI), is also a negative confounder of any common physiological exposures on health outcomes, overall and specifically by sex. Methods: We used an MR study, based on the largest overall and sex-specific genome-wide association studies of BMI (i.e., from the Genetic Investigation of ANthropometric Traits and the UK Biobank) and of relevant exposures likely affected by BMI, to assess, overall and sex-specifically, whether BMI is a negative confounder potentially obscuring effects of harmful physiological exposures. Inverse variance weighting was the main method. We assessed sex differences using a z-test. Results: BMI was a potential negative confounder for apolipoprotein B and total testosterone in men, and for both sexes regarding low-density lipoprotein cholesterol, choline, linoleic acid, polyunsaturated fatty acids, and cholesterol. Conclusions: Using BMI as an illustrative example, we demonstrate that negative confounding is an easily overlooked bias. Given negative confounding is not always obvious or known, using MR systematically to identify potential negative confounders in relevant studies may be helpful. |
| Persistent Identifier | http://hdl.handle.net/10722/365919 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jiesisibieke, Zhu Liduzi | - |
| dc.contributor.author | Schooling, C. Mary | - |
| dc.date.accessioned | 2025-11-12T00:36:32Z | - |
| dc.date.available | 2025-11-12T00:36:32Z | - |
| dc.date.issued | 2025-05-10 | - |
| dc.identifier.citation | Genes, 2025, v. 16, n. 5 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/365919 | - |
| dc.description.abstract | Background: Adequate control for confounding is key to many observational study designs. Confounders are often identified based on subject matter knowledge from empirical investigations. Negative confounders, which typically generate type 2 error, i.e., false nulls, can be elusive. Such confounders can be identified comprehensively by using Mendelian randomization (MR) to search the wealth of publicly available data systematically. Here, to demonstrate the concept, we examined whether a common positive confounder, body mass index (BMI), is also a negative confounder of any common physiological exposures on health outcomes, overall and specifically by sex. Methods: We used an MR study, based on the largest overall and sex-specific genome-wide association studies of BMI (i.e., from the Genetic Investigation of ANthropometric Traits and the UK Biobank) and of relevant exposures likely affected by BMI, to assess, overall and sex-specifically, whether BMI is a negative confounder potentially obscuring effects of harmful physiological exposures. Inverse variance weighting was the main method. We assessed sex differences using a z-test. Results: BMI was a potential negative confounder for apolipoprotein B and total testosterone in men, and for both sexes regarding low-density lipoprotein cholesterol, choline, linoleic acid, polyunsaturated fatty acids, and cholesterol. Conclusions: Using BMI as an illustrative example, we demonstrate that negative confounding is an easily overlooked bias. Given negative confounding is not always obvious or known, using MR systematically to identify potential negative confounders in relevant studies may be helpful. | - |
| dc.language | eng | - |
| dc.publisher | MDPI | - |
| dc.relation.ispartof | Genes | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.subject | body mass index | - |
| dc.subject | Mendelian randomization | - |
| dc.subject | negative confounding | - |
| dc.subject | physiological attributes | - |
| dc.title | Body Mass Index as an Example of a Negative Confounder: Evidence and Solutions | - |
| dc.type | Article | - |
| dc.description.nature | published_or_final_version | - |
| dc.identifier.doi | 10.3390/genes16050564 | - |
| dc.identifier.pmid | 40428387 | - |
| dc.identifier.scopus | eid_2-s2.0-105006728757 | - |
| dc.identifier.volume | 16 | - |
| dc.identifier.issue | 5 | - |
| dc.identifier.eissn | 2073-4425 | - |
| dc.identifier.issnl | 2073-4425 | - |
