Analysis of the largest African genomic datasets ever collected could improve understanding of diseases and aid the search for treatments.
Around a quarter of the genetic variation identified in the study, which is published in the Journal Cell today, had not been discovered before. The study also found a higher level of genetic diversity in the Ugandan population than is seen in similar studies of European populations.
Lead author Dr Deepti Gurdasani from Queen Mary said: “Most population genetics studies involve Western populations. We developed a rich, diverse resource using genome wide data from 6400 Africans, including whole genome sequencing of nearly 2000 people. Other researchers can use this data to improve the detection of genetic causes of disease – particularly those that disproportionately affect Africans and people with African ancestry.”
Dr Gurdasani said: “Modern Uganda appears to be a complex mosaic of many different communities that have migrated from surrounding regions – and from Europe and the Middle East. These migrations appear to have taken place regularly and date from just 300 years ago to around 2500 BC.”
The academic researchers collected and analysed genome-wide data from 6,400 people from a rural community in Uganda.
The team also incorporated data on 14,000 individuals from different parts of Africa. This allowed them to examine genetic determinants of traits within the population.
Dr Gurdasani said: “The combined study identified new genes associated with several diseases. These included ten new associations, of which nine are only found in Africans and would therefore not have been found in even the largest study involving Europeans.”
These discoveries included a genetic variant that causes thalassemia present in 22% of Africans that is associated with glycated haemoglobin, an indicator commonly used in the diagnosis of diabetes. This particular variant is thought to have become more frequent among African populations because it can prevent severe malaria.
As glycated haemoglobin levels are often used to diagnose diabetes, Dr Gurdasani says it is possible that diabetes may be misdiagnosed in some Africans if glycated haemoglobin is used as a diagnostic tool.
The Ugandan data also revealed differences in the importance of heritability for certain characteristics – including height and cholesterol levels. Dr Gurdasani says the latter could reflect differences in genetic and dietary factors that influence these characteristics across different populations.
Professor Ayesha Motala at the University of KwaZuluNatal in Durban, who co-led the project, said: “We hope this work will trigger larger and more diverse studies of genetic causes of disease across the region and the development of new treatments that will benefit both those living in Africa and people of African descent around the world. It underscores the importance of having globally diverse participant cohorts in genetics research.”
Before this project, which was largely funded by the United Kingdom’s Medical Research Council and Wellcome, only a few hundred whole genome sequences of African people had been completed. Researchers largely relied on genetic data from African-Americans which does not reflect the continent’s full diversity.
Lead author Dr. Segun Fatumo, Assistant Professor at the London School of Hygiene & Tropical Medicine and a Senior Scientist at MRC/UVRI & London School of Hygiene & Tropical Medicine Uganda Research Unit, said: “Our study is a major initiative at the cutting-edge of precision medicine. Discovering novel genes that are linked to common and complex diseases found in Africa, such as diabetes and cancer, could pave the way for new ways to diagnose, prevent and treat them. I am delighted to have played a lead role in identifying them.”
Another lead investigator, Professor Pontiano Kaleebu, who is the Director of the MRC/Uganda Virus Research Institute & London School of Hygiene & Tropical Medicine Uganda Research Unit, said: “Africa is central to our understanding of human origins, genetic diversity and disease susceptibility. There is a clear scientific and public health need to develop large-scale projects that examine disease susceptibility across diverse populations across the continent. That work should be integrated with initiatives to improve research capacity in Africa.”
The data was collected by researchers from universities and research institutes from Africa and the UK, led by Queen Mary University of London and including the University of KwaZuluNatal, MRC/UVRI & London School of Hygiene & Tropical Medicine Uganda Research Unit, the US National Institute of Health and the University of Cambridge.
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