News Release

A person's height impacts their risk of multiple diseases

Tall stature increases the risk of peripheral neuropathy and certain skin and bone infections

Peer-Reviewed Publication

PLOS

A person's height impacts their risk of multiple diseases

image: Researchers find that height may be a risk factor for several common conditions in adults view more 

Credit: Anna Shvets, Pexels (CC0, https://creativecommons.org/publicdomain/zero/1.0/)

Whether tall or short, a person's height increases their risk for a variety of diseases, according to a new study led by Sridharan Raghavan of the Rocky Mountain Regional VA Medical Center, U.S. publishing June 2nd in the open access journal PLOS Genetics.

Height has been a factor associated with multiple common conditions, ranging from heart disease to cancer. But scientists have struggled to determine whether being tall or short is what puts them at risk, or if factors that affect height, like nutrition and socioeconomic status, are actually to blame. In the new study, researchers set out to remove these confounding factors by looking separately at connections between various diseases and a person's actual height, and connections to their predicted height based on their genetics. The team used data from the VA Million Veteran Program, which included genetic and health information from more than 200,000 white adults and more than 50,000 Black adults.

The results confirmed previous findings that being tall is linked to a higher risk of atrial fibrillation and varicose veins, and a lower risk of coronary heart disease, high blood pressure and high cholesterol. The study also uncovered new associations between greater height and a higher risk of peripheral neuropathy, which is caused by damage to nerves on the extremities, as well as skin and bone infections, such as leg and foot ulcers.

The new study looked at more than 1,000 conditions and traits overall, making it the largest study of height and disease to date. The researchers conclude that height may be a previously unrecognized risk factor for several common conditions in adults. However, they say that more studies are needed to clarify some of these associations, and that future studies would benefit from including a larger, more diverse international population.

Raghavan adds, “Using genetic methods applied to the VA Million Veteran Program, we found evidence that adult height may impact over 100 clinical traits, including several conditions associated with poor outcomes and quality of life – peripheral neuropathy, lower extremity ulcers, and chronic venous insufficiency. We conclude that height may be an unrecognized non-modifiable risk factor for several common conditions in adults.”

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In your coverage, please use this URL to provide access to the freely available article in PLOS Genetics:
http://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1010193

Citation: Raghavan S, Huang J, Tcheandjieu C, Huffman JE, Litkowski E, Liu C, et al. (2022) A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. PLoS Genet 18(6): e1010193. https://doi.org/10.1371/journal.pgen.1010193

Author Countries: United States, China, United Kingdom

Funding: This work was supported by funding from the US Department of Veterans Affairs (https://www.research.va.gov/) MVP Program awards MVP001 I01-BX004821 (YH, KC, PWFW) and MVP003/028 I01-BX003362 (CT, PST, KMC, TLA); by the US Department of Veterans Affairs (https://www.research.va.gov/) award IK2-CX001907 (SR); by funds from the Boettcher Foundation’s Webb-Waring Biomedical Research Program (https://boettcherfoundation.org/webb-waring-biomedical-research/) (SR); by the US National Institutes of Health, National Institute for Diabetes, Digestive, and Kidney Diseases (https://www.niddk.nih.gov/research-funding) awards R01DK122503 (KEN), R01DK101855 (KEN), DK101478 (BFV), and DK126194 (BFV); by the US National Institutes of Health, National Human Genome Research Institute (https://www.genome.gov/research-funding) awards R01HG010297 (KEN) and R01HG009974 (KEN); by the US National Institutes of Health, National Heart, Lung, and Blood Institute (https://www.nhlbi.nih.gov/grants-and-training) awards R01HL142302 (KEN) and R01HL143885 (KEN); and by a Linda Pechenick Montague Investigator award (BFV). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


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