Literature DB >> 7480947

Significance of exposure assessment to analysis of cancer risk from inorganic arsenic in drinking water in Taiwan.

K G Brown1, C J Chen.   

Abstract

The primary source of evidence that inorganic arsenic in drinking water is associated with increased mortality from cancer at internal sites (bladder, liver, lung, and other organs) is a large ecologic study conducted in regions of Southwest Taiwan endemic to Blackfoot disease. The dose-response patterns for lung, liver, and bladder cancers display a nonlinear dose-response relationship with arsenic exposure. The data do not appear suitable, however, for the more refined task of dose-response assessment, particularly for inference of risk at the low arsenic concentrations found in some U.S. water supplies. The problem lies in variable arsenic concentrations between the wells within a village, largely due to a mix of shallow wells and deep artesian wells, and in having only one well test for 24 (40%) of the 60 villages. The current analysis identifies 14 villages where the exposure appears most questionable, based on criteria described in the text. The exposure values were then changed for seven of the villages, from the median well test being used as a default to some other point in the village's range of well tests that would contribute to smoothing the appearance of a dose-response curve. The remaining seven villages, six of which had only one well test, were deleted as outliers. The resultant dose-response patterns showed no evidence of excess risk below arsenic concentrations of 0.1 mg/l. Of course, that outcome is dependent on manipulation of the data, as described. Inclusion of the seven deleted villages would make estimates of risk much higher at low doses. In those seven villages, the cancer mortality rates are significantly high for their exposure levels, suggesting that their exposure values may be too low or that other etiological factors need to be taken into account.

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Year:  1995        PMID: 7480947     DOI: 10.1111/j.1539-6924.1995.tb00340.x

Source DB:  PubMed          Journal:  Risk Anal        ISSN: 0272-4332            Impact factor:   4.000


  7 in total

1.  Carcinogenic risks of inorganic arsenic in perspective.

Authors:  D M Byrd; M L Roegner; J C Griffiths; S H Lamm; K S Grumski; R Wilson; S Lai
Journal:  Int Arch Occup Environ Health       Date:  1996       Impact factor: 3.015

2.  PIN1-mediated ROS production is involved in antagonism of N-acetyl-L-cysteine against arsenic-induced hepatotoxicity.

Authors:  Huijie Zhang; Zhixin He; Ping Deng; Muxue Lu; Chao Zhou; Lingling Yang; Zhengping Yu
Journal:  Toxicol Res (Camb)       Date:  2022-07-08       Impact factor: 2.680

3.  Age adjustment in ecological studies: using a study on arsenic ingestion and bladder cancer as an example.

Authors:  How-Ran Guo
Journal:  BMC Public Health       Date:  2011-10-20       Impact factor: 3.295

Review 4.  Inorganic arsenic: a need and an opportunity to improve risk assessment.

Authors:  W R Chappell; B D Beck; K G Brown; R Chaney; R Cothern; C R Cothern; K J Irgolic; D W North; I Thornton; T A Tsongas
Journal:  Environ Health Perspect       Date:  1997-10       Impact factor: 9.031

5.  Arsenic cancer risk confounder in southwest Taiwan data set.

Authors:  Steven H Lamm; Arnold Engel; Cecilia A Penn; Rusan Chen; Manning Feinleib
Journal:  Environ Health Perspect       Date:  2006-07       Impact factor: 9.031

6.  Excretion of arsenic in urine as a function of exposure to arsenic in drinking water.

Authors:  R L Calderon; E Hudgens; X C Le; D Schreinemachers; D J Thomas
Journal:  Environ Health Perspect       Date:  1999-08       Impact factor: 9.031

7.  Mutational spectrum of p53 gene in arsenic-related skin cancers from the blackfoot disease endemic area of Taiwan.

Authors:  C H Hsu; S A Yang; J Y Wang; H S Yu; S R Lin
Journal:  Br J Cancer       Date:  1999-06       Impact factor: 7.640

  7 in total

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