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Letter
Limitations, uncertainties and competing interpretations regarding chemical exposures and diabetes
  1. Gregory G Bond1,
  2. Daniel R Dietrich2
  1. 1Manitou View Consulting, LLC, Northport, Michigan, USA
  2. 2University of Konstanz—Human and Environmental Toxicology, Konstanz, Germany
  1. Correspondence to Gregory G Bond, Manitou View Consulting, LLC, 8797 N Gills Pier Rd, Northport, MI 49670, USA; gregory.g.bond{at}gmail.com

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Trasande et al1 reported that limiting exposure to alleged endocrine disrupting chemicals would reduce the burden of adult diabetes by 13% and save €4.51 billion/year. On review, however, their paper fails to meet standards for good practices in scientific reporting—stating the limitations of the underlying data, clearly articulating uncertainties, and presenting competing views or interpretations of data.

First, Trasande et al based their analysis on an existing data set derived from an epidemiological study with significant limitations2 that were not fully discussed by the authors. The limitations include: (1) a cross-sectional design; (2) a 50% participation rate, increasing the prospects for selection bias; (3) the relatively small number of diabetes cases (N=114) from which Trasande et al extrapolate to the whole of Europe; (4) lack of information on other risk factors and (5) weak and non-statistically significant associations which could be due to reverse causality, chance, bias or confounding. Indeed, the level of uncertainty in the data suggests that the costs of alleged chemical-induced diabetes in Europe may be as low as zero.

Second, Trasande et al make a large number of assumptions in order to derive their cost estimates. They assume that: (1) findings among a small sample of Swedish residents can be extrapolated to residents aged 70–75 years throughout Europe; (2) single serum measurements of chemicals in time (rather than multiple, serial measurements) are adequate to estimate critical lifetime exposures and are representative across Europe; and (3) prevalence rates and costs of diabetes are uniform across Europe. The latter assumption is clearly invalid because the study Trasande et al relied on for their cost per case estimate3 demonstrates a 14-fold difference in costs across European countries.

Finally, the authors made several sweeping, unsubstantiated conclusions about causality, for example, ‘The epidemiological findings are likely to be causal, since they are in line with experimental mechanistic data’. They cited several ‘supporting’ references for this, but failed to cite review articles4–6 that independently concluded the available evidence was insufficient to establish causation.

Trasande et al1 fail to add to our understanding of the causes of diabetes. What is instead desperately needed4–6 are better studies exploring interactions of chemicals with β-cell function and/or mass in animal and in vitro models, at concentrations relevant for humans, and prospective epidemiology studies with questionnaire-based and serial biomarker-based assessments of exposure.

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Footnotes

  • Competing interests GGB provides consulting services to the American Chemistry Council (an organisation that represents more than 160 leading companies in the business of chemistry). DRD has no competing interests.

  • Provenance and peer review Not commissioned; internally peer reviewed.

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