Study of 2,600 TwinsUK twins finds COVID-19 symptoms partly due to genes

27th April 2020

Genes are 50% responsible for the presentation of key symptoms of COVID-19 including fever, fatigue and loss of taste and smell, according to the latest data from TwinsUK researchers.

These results suggest that some people are more susceptible to COVID-19 infection than others because of their genetic makeup.

The genetic basis of this variation in response could provide researchers with important clues for developing treatments for COVID-19 and could help identify high-risk groups of people.

The team, led by Professor Frances Williams and Professor Tim Spector, analysed data logged on the COVID19 Symptom Tracker app which has been downloaded by more than 2 million people in the UK including 2,600 twins from TwinsUK.

15,000 twins take part in TwinsUK, which is the most clinically-detailed adult twin registry in the world. Identical and non-identical twins allow researchers to understand to what extent health and disease is affected by genes – nature – and the environment – nurture.

The team used information regarding the twins’ health, symptoms and level of contact with their co-twin to develop a model to understand how much genes influence symptom presentation in COVID-19.

Genes were almost 50% responsible for the development of symptoms of delirium, fever, fatigue, shortness of breath, diarrhoea and loss of taste and smell in individuals. The environment meanwhile was responsible for the development of other symptoms such as hoarse voice, cough, chest pain and abdominal pain.

Professor Frances Williams from TwinsUK said:

“I would like to say a big thank you to all our twins for logging their symptoms and health status regularly in the app. It’s because of their tremendous commitment to health research over the years that we are able to carry out this crucial research so quickly.”

Professor Tim Spector added:

“It’s essential that everybody keeps logging their health status in the app – even if you feel well. The data you provide enables us to carry out this urgent research to understand the behaviour and progression of the virus.”

The research paper with the full findings is available in non-peer reviewed archive format at the medRxiv site here.

Hope for hearing loss

26th September 2019 – by Paz Garcia

Hand holding a hearing aid against a green background

A new study of over 250,000 volunteers has identified 44 new genes linked to age-related hearing loss.

A third of people are affected by some degree of hearing loss by the age of 65, which can lead to social isolation and disability.

Despite being such a common sensory impairment, hearing aids are the only treatment available and not much is known about the genes behind the condition.

These findings will help researchers understand how hearing loss develops and so help us find ways to treat and prevent the condition.

Professor Frances Williams, who led the collaborative research using data from UK Biobank, TwinsUK and ELSA among others, explained: 

“We now know that very many genes are involved in the loss of hearing ability as we age. This study has identified genes that we know already cause deafness in children, but it has also revealed lots of additional genes which point to new biological pathways.”

The study is the largest genetic analysis conducted to date of people who report problems with their hearing.

The work was from a joint project involving King’s College London and University College London.

What did they do?

The team wanted to identify the genetic component of adult hearing loss in the UK so that we can understand better how the condition develops as we age.

The researchers analysed the genetic data and questionnaire responses about hearing in over 250,000 participants of the UK Biobank aged 40-69 years to see which genes were associated with people who had self-reported hearing problems.

The team identified 44 new genes linked with age-related hearing loss of which 34 have not been linked to any form of hearing loss previously.

The researchers then checked their findings by studying TwinsUK and the English Longitudinal Study of Ageing.

What does this mean?

These finding will help researchers untangle the sequence of events that lead to hearing impairment as we age. Future research will investigate the biological hearing pathways influenced by these genes.

This will help us to identify possible targets for new therapies to treat and potentially prevent or delay hearing loss with age.

Wells et al., GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank, The American Journal of Human Genetics (2019).

How is bacteria linked to the development of rheumatoid arthritis?

6th March 2019 – by Paz Garcia

Old hands with rheumatoid arthritis clasped together

The way the immune system interacts with oral and gut bacteria may lead to the development of rheumatoid arthritis, according to researchers from King’s College London.

These findings may one day help us predict who is likely to develop rheumatoid arthritis, and prevent and treat the condition in new ways.

Rheumatoid arthritis is an autoimmune condition in which the body’s immune system mistakenly attacks the lining of the joints. The condition affects 400,000 people in the UK, and leads to painful, swollen joints and reduced mobility.

This is the first time researchers have investigated how genes and bacteria may work together to lead to rheumatoid arthritis.

The review was published today in the Journal of Autoimmunity.

Why did they do this research?

We know that rheumatoid arthritis is largely inherited through certain genes, but only about a third of identical twins – who have identical genes – have matching cases of the condition. This suggests that in many cases, genes alone are not enough to lead to rheumatoid arthritis.

Researchers have also previously found differences in the oral, lung and gut bacteria of people diagnosed with rheumatoid arthritis and those without.

In this work, the team decided to review the available evidence to see how certain genetic factors and bacteria in the body – the microbiome – may lead to rheumatoid arthritis.

The work was led by Philippa Wells, a PhD student at the Department of Twin Research and Genetic Epidemiology at King’s College London.

What did they find?

The team analysed many previous studies that looked at how genes and the microbiome were linked with rheumatoid arthritis.

Based on their analysis, the researchers suggested that certain genes to do with the immune system are the key link between genes, the microbiome and rheumatoid arthritis.

Genes largely determine how the immune system behaves. The researchers proposed that the immune system then responds inappropriately to certain bacteria in the body, which ultimately leads to the immune system mistakenly attacking the joints.

What does this mean?

This is the first time researchers have investigated how interactions between genes and bacteria may lead to rheumatoid arthritis.

In the future, we may be able to use the microbiome to predict whether and when someone might develop rheumatoid arthritis. Researchers could also develop treatment strategies for the condition that work through targeting bacteria in the body.

Researcher Philippa Wells explained:

“These methods let us investigate what is happening with the microbiome before onset of rheumatoid arthritis, as well as unpicking what influences the microbiome differences we see in people with rheumatoid arthritis.

“From that, we can gain insight in to the direction of influence, i.e whether changes in the microbiome cause rheumatoid arthritis or vice versa, and get a clearer idea of the underlying biology.

“This will be important groundwork for future clinically focused studies.”

What’s the next step?

In their paper, the researchers stress that it will be important to understand the effect of current rheumatoid arthritis medication on the microbiome.

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