France gets 80% of its electricity from nuclear energy. France is a target for those who are against nuclear energy to try to find any evidence of negative health or economic effects to discredit France’s nuclear energy success.
The hypothetical risk in the flawed study was an increase based on a statistical fluctuation. In addition, the study did not address confounding factors which could impact the data. The putative increase in leukemia risk therefore cannot be justifiably attributed to very small radiation doses associated with the operation of the Nuclear power plants.
1. The authors have not one datum in Table 2 (Sermage-Faure et al. 2012) that shows a statistically significant increase in cancer risk, whether for children under 5 or under 15 years of age, in either the interval 1990–2001 or 2002–2007. Only by data dredging and subdividing the numbers into smaller time intervals and other discriminatory indices in Table 4 (Sermage-Faure et al. 2012), can they produce a few showing statistical significance. But then, the numbers of children included in each time interval are small.
2. the results in the abstract are based on only 14 cancer cases near 19 NPPs. Fourteen cases are too few for a clinically significant result. Fourteen cases near 19 NPPs are on average 0.7 cases per NPP.
3. neither any confounding factor nor individual history of the children (especially their migrations) was taken into consideration. These omissions and the mentioned small-sample-size-related statistical problems invalidate the claimed association of cancer risk with NPP proximity.
Additional weak points of the analysis were diligently mentioned by the authors (Sermage-Faure et al. 2012). First, no correlation was found between cancer cases and radioactive releases from NPPs. Second, similar French investigations several years earlier failed to find an increase in risk (White-Koning et al. 2004; Evrard et al. 2006; Laurier et al. 2008). And the evaluation over a wider time period (1990–2007) did not show a statistically significant risk increase. Third, total accumulated doses over the time period 2002–2007 were in the range of microsieverts – several orders of magnitude lower than the variations in natural background radiation. Fourth, lower doses were received by children living up to 5 km from the NPP, where the risk was estimated to be higher, while no risk increase was found among children who received the highest doses. These four weaknesses alone should have been sufficient to invalidate any claimed association between NPP operation and cancer, without the three points raised in this Letter. One can add also that despite the authors’ reluctance to unambiguously relate the leukemia incidence to the NPP emissions, they nevertheless suggest that leukemia is a consequence of radiation exposure from NPP operation. We point out in the present Letter why this suggestion is not justified.
Attribution of an excess risk of cancers to nearby NPPs is a well known practice, even though many independent studies, such as COMARE (2011), CANUPIS (Spycher et al. 2011) or RADICON (2013), have demonstrated no correlation between radiation exposures around NPPs and cancer incidence. Observed increases can be attributed to population mixing, as pointed out in the most recent extensive review of childhood leukemia around NPPs
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