2014
DOI: 10.1136/oemed-2013-101795
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Diabetic ketoacidosis following chlorothalonil poisoning: Table 1

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Cited by 9 publications
(5 citation statements)
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“…Although humans are not exposed to alloxan or sreptozotocin, they are used in animal research on diabetes. Initial human evidence that synthetic chemicals promote the development of diabetes came from patients accidentally or intentionally exposed to pyrinuron (Vacor) [453]. Exposure to this rodenticide resulted in β-cell destruction and the development of type 1 diabetes [454].…”
Section: Mdcs and Metabolism-relevant Diseasesmentioning
confidence: 99%
“…Although humans are not exposed to alloxan or sreptozotocin, they are used in animal research on diabetes. Initial human evidence that synthetic chemicals promote the development of diabetes came from patients accidentally or intentionally exposed to pyrinuron (Vacor) [453]. Exposure to this rodenticide resulted in β-cell destruction and the development of type 1 diabetes [454].…”
Section: Mdcs and Metabolism-relevant Diseasesmentioning
confidence: 99%
“…Eight patients with acute chlorothalonil poisoning have been reported, only six of whom ingested the fungicide. 9 , 10 A case series from Sri Lanka reported six patients with intentional chlorothalonil ingestions (and one with a mild inhalational injury). 9 The six patients ingesting chlorothalonil developed a burning sensation of the mouth, throat, and epigastrium, and had dysphagia and vomiting.…”
Section: Discussionmentioning
confidence: 99%
“…The only renal-related effect mentioned in this case report was the presence of intense ketonuria, as expected with DKA; serum markers of kidney function (BUN, creatinine) were not reported. 10 …”
Section: Discussionmentioning
confidence: 99%
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“…While accidental or intentional ingestions of a single chemical may be sufficient to cause diabetes in select circumstances (e.g. the rodenticide Vacor 9 and the fungicide chlorothalonil 10 ), it is unlikely that a single chemical will be sufficient to explain the dramatic explosion in global diabetes rates. However, as there are tens of thousands of unique chemicals to which humans are potentially exposed, coordinate exposure to multiple EDCs that additively antagonize critical pathways regulating energy metabolism through complimentary mechanisms may be sufficient to promote cardiometabolic dysfunction, whereas a single signaling disruptor in isolation may be insufficient to drive significant disease.…”
Section: Introductionmentioning
confidence: 99%