23andMe Launches Its First NIH Funded Study

  By Amy Kiefer and Kim Barnholt 23andMe is excited to announce the launch of our first National Institutes of Health (NIH) funded research project. In  the fall of 2010, 23andMe received a NIH Small Business Innovative Research Grant (SBIR) to validate our web-based approach to pharmacogenomics research. The NIH is the largest source of medical research funding in the world. Through its support of innovative training programs and scientific projects, the NIH facilitates medical discoveries that lead to improved health and quality of life. NIH grants are highly coveted by industry scientists and academics alike.  In addition to the funding itself, the NIH grant  demonstrates support  and recognition of our work by a leading governmental research agency. Pharmacogenomics aims to  transform  the “one size fits all” approach to drug use and development to a more personalized one in which an individual’s genotype helps determine the most effective and least toxic medication. 23andMe’s Drug Response  reports provide a glimpse into the potential power of this approach. For different individuals, the same drug could be lifesaving, have no effect, or even be life threatening. The initial phase of 23andMe’s pharmacogenomics project  will attempt  to replicate known genetic effects that influence the efficacy and tolerability of three classes of medications: Warfarin, a commonly prescribed blood thinner; proton pump inhibitors, the most frequently prescribed medications for acid reflux; and nonsteroidal anti-inflammatory drugs (NSAIDs), such as aspirin, ibuprofen, and naproxen. Our customers who have taken or are taking any of these medications should look for these surveys in the coming months. A subset of people who complete each of these surveys will  also  be contacted for phone interviews to help assess the quality of information we are able to collect over the web. The purpose of this first phase is similar to that of  our first research publication: to demonstrate that we can replicate known genetic  associations using the web-based survey data volunteered by our customers. Our pharmacogenomics project is distinct,  however, in that collecting self-reported medication information via the web presents unique challenges.  For example, recall of medication use and side effects may be poor and difficult  for individuals to accurately report. The use of multiple medications may  also complicate efforts to isolate which medications cause specific responses or side effects. Still, the potential rewards are tremendous  — validation of a large-scale, cost-effective, and rapid approach for discovering new pharmacogenomic markers would be a significant contribution to personalized medicine. We hope you share our excitement about  receiving  this funding for one of our top research priorities:  the advancement of personalized medicine through genetic studies.  In the spirit of the  23andWe research paradigm,  we will continue to work together to make  research discoveries and learn more about the information encoded in our genomes. View the official press release here.
  • Teddy Devereux

    Congratulations on getting an NIH grant! This is very exciting and the type of thing I hoped would happen when I signed up as a customer.


    Very exciting news, I wanted to contribute to 23andWe/23andMe to enable this type of development which will hopefully be the FIRST of many. I am interested in contributing to development of a protocol which would get FRESH SARCOMA TISSUE TO THE MAJOR RESEARCH CENTERS IN THE UNITED STATES. For example, the two tumors found in MY uterus were 12.5 cm and 7.5 cm in size. A small amount of fresh tissue was retained by RUSH, where I had my surgery, however, the remainder was simply “thrown away”. It was my wish that some go to SFA; Memorial Sloan Kettering; Cedars-Sinai; Dr. Lois Ramondetta and the hospital in TX, whose name I can’t recall at the moment; and any researchers who would want a piece of FRESH tissue. I wish I knew THEN what I know NOW.

  • ted

    Hey Swiss. A project to genetically map populations and describe there relatedness is happening here: http://dodecad.blogspot.com/2010/12/open-ended-submission-opportunity-for.html

    If you’ve tested with 23andme please visit the site and help discover who the Swiss are.

  • Congrats! This is potentially huge. I believe that within a decade patients will be genetically profiled before being put on certain types of medication (e.g. statins). My profile from 23andme has already been used by my doctor to optimize my medications. The upcoming NIH-funded study will be a step forward for pharmacogenomics.