Literature DB >> 11778666

Chronic arsenic toxicity in Bangladesh and West Bengal, India--a review and commentary.

M M Rahman1, U K Chowdhury, S C Mukherjee, B K Mondal, K Paul, D Lodh, B K Biswas, C R Chanda, G K Basu, K C Saha, S Roy, R Das, S K Palit, Q Quamruzzaman, D Chakraborti.   

Abstract

Fifty districts of Bangladesh and 9 districts in West Bengal, India have arsenic levels in groundwater above the World Health Organization's maximum permissible limit of 50 microg/L. The area and population of 50 districts of Bangladesh and 9 districts in West Bengal are 118,849 km2 and 104.9 million and 38,865 km2 and 42.7 million, respectively. Our current data show arsenic levels above 50 microg/ L in 2000 villages, 178 police stations of 50 affected districts in Bangladesh and 2600 villages, 74 police stations/blocks of 9 affected districts in West Bengal. We have so far analyzed 34,000 and 101,934 hand tube-well water samples from Bangladesh and West Bengal respectively by FI-HG-AAS of which 56% and 52%, respectively, contained arsenic above 10 microg/L and 37% and 25% arsenic above 50 microg/L. In our preliminary study 18,000 persons in Bangladesh and 86,000 persons in West Bengal were clinically examined in arsenic-affected districts. Of them, 3695 (20.6% including 6.11% children) in Bangladesh and 8500 (9.8% including 1.7% children) in West Bengal had arsenical dermatological features. Symptoms of chronic arsenic toxicity developed insidiously after 6 months to 2 years or more of exposure. The time of onset depends on the concentration of arsenic in the drinking water, volume of intake, and the health and nutritional status of individuals. Major dermatological signs are diffuse or spotted melanosis, leucomelanosis, and keratosis. Chronic arsenicosis is a multisystem disorder. Apart from generalized weakness, appetite and weight loss, and anemia, our patients had symptoms relating to involvement of the lungs, gastrointestinal system, liver, spleen, genitourinary system, hemopoietic system, eyes, nervous system, and cardiovascular system. We found evidence of arsenic neuropathy in 37.3% (154 of 413 cases) in one group and 86.8% (33 of 38 cases) in another. Most of these cases had mild and predominantly sensory neuropathy. Central nervous system involvement was evident with and without neuropathy. Electrodiagnostic studies proved helpful for the diagnosis of neurological involvement. Advanced neglected cases with many years of exposure presented with cancer of skin and of the lung, liver, kidney, and bladder. The diagnosis of subclinical arsenicosis was made in 83%, 93%, and 95% of hair, nail and urine samples, respectively, in Bangladesh; and 57%, 83%, and 89% of hair, nail, and urine samples, respectively in West Bengal. Approximately 90% of children below 11 years of age living in the affected areas show hair and nail arsenic above the normal level. Children appear to have a higher body burden than adults despite fewer dermatological manifestations. Limited trials of 4 arsenic chelators in the treatment of chronic arsenic toxicity in West Bengal over the last 2 decades do not provide any clinical, biochemical, or histopathological benefit except for the accompanying preliminary report of clinical benefit with dimercaptopropanesulfonate therapy. Extensive efforts are needed in both countries to combat the arsenic crisis including control of tube-wells, watershed management with effective use of the prodigious supplies of surface water, traditional water management, public awareness programs, and education concerning the apparent benefits of optimal nutrition.

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Year:  2001        PMID: 11778666     DOI: 10.1081/clt-100108509

Source DB:  PubMed          Journal:  J Toxicol Clin Toxicol        ISSN: 0731-3810


  50 in total

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Journal:  Occup Environ Med       Date:  2005-09       Impact factor: 4.402

2.  Anthropometric measures at birth and early childhood are associated with neurodevelopmental outcomes among Bangladeshi children aged 2-3years.

Authors:  Jane J Lee; Kush Kapur; Ema G Rodrigues; Md Omar Sharif Ibne Hasan; Quazi Quamruzzaman; Robert O Wright; David C Bellinger; David C Christiani; Maitreyi Mazumdar
Journal:  Sci Total Environ       Date:  2017-07-27       Impact factor: 7.963

3.  Overexpression of hsa-miR-186 induces chromosomal instability in arsenic-exposed human keratinocytes.

Authors:  Jiguo Wu; Ana P Ferragut Cardoso; Vanessa A R States; Laila Al-Eryani; Mark Doll; Sandra S Wise; Shesh N Rai; J Christopher States
Journal:  Toxicol Appl Pharmacol       Date:  2019-06-06       Impact factor: 4.219

4.  A follow-up study of the development of skin lesions associated with arsenic exposure duration.

Authors:  Binggan Wei; Jiangping Yu; Chang Kong; Hairong Li; Linsheng Yang; Yajuan Xia; Kegong Wu
Journal:  Environ Geochem Health       Date:  2018-06-14       Impact factor: 4.609

5.  Arsenic-induced decreases in the vascular matrix.

Authors:  Allison M Hays; R Clark Lantz; Laurel S Rodgers; James J Sollome; Richard R Vaillancourt; Angeline S Andrew; Joshua W Hamilton; Todd D Camenisch
Journal:  Toxicol Pathol       Date:  2008-09-23       Impact factor: 1.902

6.  Arsenic levels in rice grain and assessment of daily dietary intake of arsenic from rice in arsenic-contaminated regions of Bangladesh--implications to groundwater irrigation.

Authors:  Mohammad Mahmudur Rahman; Gary Owens; Ravi Naidu
Journal:  Environ Geochem Health       Date:  2009-01-14       Impact factor: 4.609

7.  Chronic arsenic exposure impairs macrophage functions in the exposed individuals.

Authors:  Nilanjana Banerjee; Saptarshi Banerjee; Rupashree Sen; Apurba Bandyopadhyay; Nilendu Sarma; Papiya Majumder; Jayanta K Das; Mitali Chatterjee; Syed N Kabir; Ashok K Giri
Journal:  J Clin Immunol       Date:  2009-06-10       Impact factor: 8.317

8.  The NRF2-mediated oxidative stress response pathway is associated with tumor cell resistance to arsenic trioxide across the NCI-60 panel.

Authors:  Qian Liu; Hao Zhang; Lisa Smeester; Fei Zou; Matt Kesic; Ilona Jaspers; Jingbo Pi; Rebecca C Fry
Journal:  BMC Med Genomics       Date:  2010-08-13       Impact factor: 3.063

9.  Arsenic toxicity in the human nerve cell line SK-N-SH in the presence of chromium and copper.

Authors:  Ligang Hu; Justin B Greer; Helena Solo-Gabriele; Lynne A Fieber; Yong Cai
Journal:  Chemosphere       Date:  2013-03-06       Impact factor: 7.086

10.  Combined administration of taurine and monoisoamyl DMSA protects arsenic induced oxidative injury in rats.

Authors:  Swaran J S Flora; Swapnila Chouhan; Gurusamy M Kannan; Megha Mittal; Harimohan Swarnkar
Journal:  Oxid Med Cell Longev       Date:  2008 Oct-Dec       Impact factor: 6.543

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