"We estimate that an average of 3 percent of the population have receptors that contain mutations which can alter the effect of medicine," says first author of the study, PhD Fellow Alexander Hauser from the Department of Drug Design and Pharmacology at the University of Copenhagen.
2This might mean that the medicine simply works less efficiently. It can also mean that the medicine does not work at all or causes adverse effects on patients," adds Madan Babu, last author of the study, from the MRC Lab of Molecular Biology in Cambridge, where Hauser conducted this research.
The researchers have analysed the mutations in human GPCRs by using whole genome sequencing data from the 1,000 Genomes project with about 2,500 participants as well as exome data from the ExAC project with over 60,000 participants.
They then used structural data to infer critical sites in GPCRs to uncover which mutations are more likely to alter the outcome of medicine.
"The 3 percent of the affected population is an average. For some important receptors, it is way more. For instance, the relevant mutations occur in 69 percent of people in the GLP1 receptor that is the target of diabetes medicine and in 86 percent of people in the CNR2 receptor that is used as a target for medicine to relieve nausea induced by chemotherapy. But of course, we cannot know every person's genome and so these are estimates based on the data sets available," says Alexander Hauser.
The researchers use their findings and sales data for the 279 GPCR-relevant drugs from the National Health Service in the UK to estimate how much money is spent on medicine with little or no effect.
As a conservative estimate, they find the economic burden on the UK National Health Service to be at least 14 million pounds annually, taking into account the number of people with mutations in both copies of the gene in important sites of the receptor target.
"The prevalence and potential impact of variation in drug response between individuals is a strong argument for further researching this field. It also constitutes a fine example of why personalised medicine might be the way forward; even when we are talking about common drugs," says Hauser.
Hauser AS, Chavali S, Masuho I, Jahn LJ, Martemyanov KA, Gloriam DE, Babu MM.
Pharmacogenomics of GPCR Drug Targets.
Cell. 2017 Dec 8. pii: S0092-8674(17)31384-3. doi: 10.1016/j.cell.2017.11.033.