̽��ֱ��

Empathy has two parts: the ability to recognize another person’s thoughts and feelings, and the ability to respond with an appropriate emotion to someone else’s thoughts and feelings. ̽��ֱ��first part is called ‘cognitive empathy’ and the second part ‘affective empathy’.

Fifteen years ago, a team of scientists at the ̽��ֱ�� of Cambridge developed the Empathy Quotient (EQ), a brief self-report measure of empathy. ̽��ֱ��EQ measures both parts of empathy.

Previous research showed that some of us are more empathetic than others, and that on average, women are slightly more empathetic than men. It also showed that, on average, autistic people score lower on the EQ, and that this was because they struggle with cognitive empathy, even though their affective empathy may be intact.

In a new study published in the journal Translational Psychiatry, the Cambridge team, working with the genetics company 23andMe and a team of international scientists, report the results of the largest genetic study of empathy using information from more than 46,000 23andMe customers. ̽��ֱ��customers all completed the EQ online and provided a saliva sample for genetic analysis.

̽��ֱ��study was led by Varun Warrier, a Cambridge PhD student, and Professors Simon Baron-Cohen, Director of the Autism Research Centre at Cambridge ̽��ֱ��, Thomas Bourgeron, of the ̽��ֱ�� Paris Diderot and the Institut Pasteur, and David Hinds, Principal Scientist at 23andMe.

̽��ֱ��new study has three important results. First, it found that how empathetic we are is partly due to genetics. Indeed, a tenth of this variation is due to genetic factors. This confirms previous research examining empathy in identical versus non-identical twins.

Second, the new study confirmed that women are on average more empathetic than men. However, this difference is not due to our DNA as there were no differences in the genes that contribute to empathy in men and women.

This implies that the sex difference in empathy is the result of other non-genetic biological factors, such as prenatal hormone influences, or non-biological factors such as socialisation, both of which also differ between the sexes.

Finally, the new study found that genetic variants associated with lower empathy are also associated with higher risk for autism.��

Varun Warrier said: “This is an important step towards understanding the small but important role that genetics plays in empathy. But keep in mind that only a tenth of individual differences in empathy in the population are due to genetics. It will be equally important to understand the non-genetic factors that explain the other 90%.”

Professor Thomas Bourgeron added: “This new study demonstrates a role for genes in empathy, but we have not yet identified the specific genes that are involved. Our next step is to gather larger samples to replicate these findings, and to pin-point the precise biological pathways associated with individual differences in empathy.”

Dr David Hinds said: “These are the latest findings from a series of studies that 23andMe have collaborated on with researchers at Cambridge. Together these are providing exciting new insights into the genetics influences underlying human behaviour.”

Professor Simon Baron-Cohen added: “Finding that even a fraction of why we differ in empathy is due to genetic factors helps us understand people such as those with autism who struggle to imagine another person’s thoughts and feelings. This can give rise to disability no less challenging than other kinds of disability, such as dyslexia or visual impairment. We as a society need to support those with disabilities, with novel teaching methods, work-arounds, or reasonable adjustments, to promote inclusion.”

This study also benefitted from support from the Medical Research Council, the Wellcome Trust, the Institut Pasteur, the CNRS, the ̽��ֱ�� Paris Diderot, the Bettencourt-Schueller Foundation, the Cambridge Commonwealth Trust, and St John’s College, Cambridge.

Reference
, by V Warrier, R Toro, B Chakrabarti, iPSYCH-Broad Autism Group, Grove J, Borglum AD, D Hinds, T Bourgeron, and S Baron-Cohen. Translational Psychiatry. DOI: 10.1038/s41398-017-0082-6