News Release 

Decoding the genetics that drive disease

University of South Australia

Research News

IMAGE

IMAGE: Some human genes traditionally labelled as 'bad' are not always what they seem. view more 

Credit: Image by Gerd Altmann from Pixabay

From Alzheimer's to obesity, life can change dramatically if you discover you have a genetic risk of disease. Now, a new study from the Australian Centre for Precision Health, University of South Australia is challenging these predispositions, showing that some of the genes traditionally labelled as 'bad' are not always what they seem.

Examining the three main variants (ε4, ε3, and ε2) of the apolipoprotein E (APOE) gene involved in the metabolism of fats in the body - researchers found that both the typically 'bad' variant, APOE ε4, and the 'good' variant, APOE ε2 can increase as well as decrease the risk of disease.

Overall, the research revealed APOE-associations with 18 different diseases.

Lead researcher and geneticist, UniSA's Dr Amanda Lumsden says the findings provide valuable insights about how the APOE gene impacts health and disease.

"APOE-ε4 is notoriously the greatest known risk factor for late onset Alzheimer's disease, and is also connected to cardiovascular disease risk," Dr Lumsden says.

"Yet, despite its reputation, our research shows it also has qualities that can protect against a range of illnesses, including obesity, type 2 diabetes, chronic airway obstruction, and liver disease.

"Conversely, we found that the rarer APOE ε2 gene variant - which is often considered protective and beneficial to health - can increase the risk of several conditions including peripheral vascular disease, stomach ulcers, diseases of the cervix, and bunions."

The study assessed APOE-associated risks across a spectrum of more than 950 diseases, using information from 337,484 participants in the UK Biobank. Brain neuroimaging, blood biochemistry, body measurement and lung function biomarkers for the same population were also used to support the APOE-associations.

World-renowned genetic epidemiologist and Senior Principal Research Fellow at SAHMRI, Professor Elina Hyppönen*, says the study gives hope to people who may carry a genotype that has been classified as 'harmful'.

"An awareness of a genetic susceptibility can cause notable distress, especially if there is little that can be done to prevent that disease," Professor Hyppönen says.

"Here, we show that the same variant that causes harm with respect to some diseases, can be beneficial from other aspects of health, so it's not all doom and gloom based on your genes.

"Of course, it can be helpful to understand our genetic vulnerabilities, as this can motivate us to make positive lifestyle changes that can reduce the risk.

"This is true of several diseases. In our earlier work, we showed that by living a healthy lifestyle you can help mitigate the risk of dementia, even when a person has an elevated genetic risk.

"So, despite what your genes say about predispositions to disease, there are other ways to help you stay healthy and negate the risks."

###

Notes to editors:

* Professor Elina Hyppönen has multiple highly cited papers which are ranked among the top 1 per cent of papers in the field globally, Clarivate, Web of Science, Data retrieved 11-9-20

The newly published paper - Apolipoprotein E (APOE) genotype-associated disease risks: a phenome-wide, registry-based, case-control study utilising the UK Biobank - can be accessed here: https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(20)30330-3/fulltex

..........................................................................................................................................

Media contact: Annabel Mansfield P: +61 8 8302 0351 M: +61 417 717 504

E: Annabel.Mansfield@unisa.edu.au

Researchers: Dr Amanda Lumsden E: Amanda.Lumsden@unisa.edu.au

Professor Elina Hypponen E: Elina.Hypponen@unisa.edu.au

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.