BACKGROUND: There is an ongoing discussion about the risks of di(2-ethylhexyl) phthalate (DEHP) exposure for the general population as well as for specific subgroups in various medical settings. Haemodialysis patients certainly belong to the group with the highest exposure taking into account the repeated treatments over a long period of time. Many studies have shown that DEHP metabolites are more active with regard to cellular responses than DEHP itself. Although 4-heptanone has been shown to be a DEHP metabolite in rats, this has never been tested in humans. On the other hand, 4-heptanone was reported to be associated with diabetes mellitus. METHODS: After establishing analytical methods for all postulated metabolites, we analysed (i) plasma samples from 50 patients on haemodialysis and 50 controls; (ii) urine samples from 100 diabetic patients and 100 controls; and (iii) urine samples from 10 controls receiving DEHP intravenously. RESULTS: 4-Heptanone concentrations in urine did not differ between controls (128.6+/-11.4 micro g/l, mean+/- SEM) and diabetic patients (131.2+/-11.6 micro g/l) but were significantly elevated in plasma from haemodialysis patients (95.9+/-9.6 micro g/l) compared with controls (10.4+/-0.5 micro g/l). Exposure to DEHP led to a significant increase (P<0.001) of the metabolite 4-heptanone and all the proposed intermediates in urine of healthy persons within 24 h. CONCLUSIONS: These studies show that 4-heptanone is not associated with diabetes but is a major DEHP metabolite in humans. Studies concerning the toxicity of DEHP in haemodialysis patients and other highly exposed groups should therefore include 4-heptanone together with DEHP and its primary metabolites mono(2-ethylhexyl) phthalate (MEHP) and 2-ethylhexanol.
BACKGROUND: There is an ongoing discussion about the risks of di(2-ethylhexyl) phthalate (DEHP) exposure for the general population as well as for specific subgroups in various medical settings. Haemodialysis patients certainly belong to the group with the highest exposure taking into account the repeated treatments over a long period of time. Many studies have shown that DEHP metabolites are more active with regard to cellular responses than DEHP itself. Although 4-heptanone has been shown to be a DEHP metabolite in rats, this has never been tested in humans. On the other hand, 4-heptanone was reported to be associated with diabetes mellitus. METHODS: After establishing analytical methods for all postulated metabolites, we analysed (i) plasma samples from 50 patients on haemodialysis and 50 controls; (ii) urine samples from 100 diabeticpatients and 100 controls; and (iii) urine samples from 10 controls receiving DEHP intravenously. RESULTS:4-Heptanone concentrations in urine did not differ between controls (128.6+/-11.4 micro g/l, mean+/- SEM) and diabeticpatients (131.2+/-11.6 micro g/l) but were significantly elevated in plasma from haemodialysis patients (95.9+/-9.6 micro g/l) compared with controls (10.4+/-0.5 micro g/l). Exposure to DEHP led to a significant increase (P<0.001) of the metabolite 4-heptanone and all the proposed intermediates in urine of healthy persons within 24 h. CONCLUSIONS: These studies show that 4-heptanone is not associated with diabetes but is a major DEHP metabolite in humans. Studies concerning the toxicity of DEHP in haemodialysis patients and other highly exposed groups should therefore include 4-heptanone together with DEHP and its primary metabolites mono(2-ethylhexyl) phthalate (MEHP) and 2-ethylhexanol.
Authors: Luz M Iribarne-Durán; Francisco Artacho-Cordón; Manuela Peña-Caballero; José M Molina-Molina; Inmaculada Jiménez-Díaz; Fernando Vela-Soria; Laura Serrano; José A Hurtado; Mariana F Fernández; Carmen Freire; Nicolás Olea Journal: Environ Health Perspect Date: 2019-11-27 Impact factor: 9.031
Authors: Andreas Leiherer; Daria Ślefarska; Marcis Leja; Christine Heinzle; Axel Mündlein; Ilze Kikuste; Linda Mezmale; Heinz Drexel; Chris A Mayhew; Paweł Mochalski Journal: Front Mol Biosci Date: 2021-01-11
Authors: Daria Ślefarska-Wolak; Christine Heinzle; Andreas Leiherer; Clemens Ager; Axel Muendlein; Linda Mezmale; Marcis Leja; Alejandro H Corvalan; Heinz Drexel; Agnieszka Królicka; Gidi Shani; Christopher A Mayhew; Hossam Haick; Paweł Mochalski Journal: Molecules Date: 2022-06-22 Impact factor: 4.927
Authors: Nikolaos Pagonas; Wolfgang Vautz; Luzia Seifert; Rafael Slodzinski; Joachim Jankowski; Walter Zidek; Timm H Westhoff Journal: PLoS One Date: 2012-09-25 Impact factor: 3.240