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Editorials

Predictive genetic testing for type 2 diabetes

BMJ 2006; 333 doi: https://doi.org/10.1136/bmj.38953.598947.80 (Published 07 September 2006) Cite this as: BMJ 2006;333:509
  1. A Cecile J W Janssens, epidemiologist (a.janssens{at}erasmusmc.nl),
  2. Marta Gwinn, epidemiologist,
  3. Rodolfo Valdez, epidemiologist,
  4. K M Venkat Narayan, chief,
  5. Muin J Khoury, director
  1. Department of Public Health, Erasmus MC University Medical Centre Rotterdam, 3000 CA Rotterdam, Netherlands
  2. Centers for Disease Control and Prevention, Atlanta, GA 30341, USA

    May raise unrealistic expectations

    The discovery earlier this year that a variant of the TCF7L2 (transcription factor 7-like 2) gene is associated with type 2 diabetes was reported in a front page story in the New York Times.12 The principal investigator, Kari Stefansson, told the newspaper that the discovery could lead to a diagnostic test to identify people who carry the variant gene. People who knew of their extra risk, he said, would be motivated to avoid the lifestyle habits that lead to diabetes. A Scottish scientist headed the research team, which led the Glasgow Herald to report, “Discovery of holy grail will help scientists treat diabetes.”3

    Undeniably this discovery is noteworthy. Type 2 diabetes is a leading cause of morbidity and mortality in the developed world and is increasing in prevalence worldwide. The association is robust—the finding has been replicated in three large independent study populations and offers potential new insight into the pathobiology of diabetes. Yet the claim that this knowledge will lead to a diagnostic test and hence to disease prevention—now routine for such genetic discoveries—may not be true. We believe that this syllogism (a logical argument in which one proposition (the conclusion) is inferred from two others (the premises)) oversimplifies the research findings and the challenge of translation and, above all, misleads the public.

    The investigators estimated a 21% population attributable risk for the risk genotypes. This means that 21% of cases of the disease can be prevented when the negative effects of the genetic “exposure” are eliminated. However, by itself, a large population attributable risk does not indicate what efforts are needed to reduce the prevalence of diabetes in terms of the number who need intervention or the effectiveness of the preventive strategy. If this discovery led to a 100% effective intervention that specifically targeted the effects of the genetic variant, 45% of the general population would need to receive this intervention to prevent 21% of diabetes cases. If we assume an overall lifetime risk of diabetes of 33%,4 88% of heterozygous carriers and 63% of homozygotes might not benefit from this intervention because they would not develop diabetes despite their TCF7L2 carrier status or they would develop diabetes from other causes. An intervention that specifically targets the effects of TCF7L2 variants would need to be cheap, harmless, and burdenless to warrant such substantial overtreatment.

    Alternatively, as Kari Stefansson suggested, the genetic test could identify people at high risk who would benefit from appropriate advice on diet and physical activity (although this advice is applicable to all). The risk of diabetes is increased from 33% to 63% in homozygous TCF7L2 carriers (7% of the population), but the risk is increased from 33% to only 38% in heterozygous carriers (38% of the population). Would these figures provide enough incentive for carriers to change their lifestyles?5

    Only a month before online publication of the discovery of TCF7L2, another study evaluated the simultaneous testing of PPARG (peroxisome proliferative activated receptor γ) and CAPN10 (calpain 10) SNP43/44 (single nuclear protein 43/44) genotypes and claimed that “genetic testing might become a future approach to identify people at risk of developing type 2 diabetes.”6 This conclusion was based on the finding that carriers of the PPARG PP and CAPN10 SNP43/44 GG/TT genotypes who were obese and had raised fasting plasma glucose values, had a 21.2-fold increased risk for type 2 diabetes compared with non-obese non-carriers with normal fasting plasma glucose. We showed that testing for these genetic variants would not improve the prediction of type 2 diabetes over body mass index and fasting plasma glucose concentration.7

    Inferences about the public health applications of genetic testing are often based on single measures of association or indicators of test performance, such as the risk ratio or population attributable risk. Predictive genetic testing is useful when the value it adds to existing interventions outweighs the additional personal and social costs. This requires a complete evaluation of the test's performance characteristics, including sensitivity and specificity; its positive and negative predictive value in the population to be tested; the likelihood ratio of positive and negative test results; and the rates of false positive and false negative test results. These data are only part of the evidence base needed to recommend a test, which also includes information about effectiveness relative to existing alternatives, side effects, and costs.8 A risk ratio or population attributable risk alone cannot predict the potential usefulness of genetic testing.

    News about genetic associations with type 2 diabetes and the potential for predictive testing was quickly picked up by patient organisations.912 Ultimately, genetic discoveries may lead to better understanding of the disease process and to better therapeutic and preventive interventions. In the mean-time, scientists and the media are responsible for accurately and carefully interpreting the implications of studies of genetic associations for the benefit of the general public. Raising unrealistic expectations—even inadvertently—could distract attention from what can be done by applying what we already know to prevent diabetes and its complications.13

    Footnotes

    • Competing interests None declared.

    References

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