Elevated copper in urine of Bangladeshi ethnic group living in the United Kingdom

Inductively Coupled Plasma – Mass Spectroscopy (ICP-MS) was used to monitor urinary selenium, copper and zinc in a group of Bangladeshi (n = 54), Indian (n = 25), Pakistani (n = 21), and White Caucasian (n = 23) volunteers living in the UK. The most striking findings were far higher urinary copper levels (P < 0.001) in the Bangladeshi group (median: 30.2 μg Cu/l) compared to other ethnicities (15.6 μg Cu/l, Pakistani; 14.8 μg Cu/l, Indian; 10.5 μg Cu/l, Caucasians) and to reference values reported for the UK population. Although no significant difference was found for Zn (P = 0.22; medians: 430 μg Zn/l for Bangladeshis, 377 μg Zn/l for Pakistani, 350 μg Zn/l for Caucasians, 355 μg Zn/l for Indians), a significantly (P < 0.001) higher Cu:Zn ratio was found for the Bangladeshis. Urinary Se of Bangladeshis (17.6 μg Se/l) was significantly (P < 0.001) higher compared to Indians (13.8 μg Se/l) and Pakistani (4.1 μg Se/l), although urinary selenium was generally within the reported reference values reported for the UK population. Exposure to copper via ethnic food consumption or altered copper metabolism may contribute to higher levels of Cu and Cu:Zn ratio in the Bangladeshi group. Previous studies have correlated high serum copper levels to cardiovascular diseases (CVD), liver cirrhosis, chronic hepatitis and hepatocellular carcinoma (HCC). Bangladeshis have higher than UK average mortality from HCC and a disproportionately higher incidence of CVD. The high urinary Cu levels and Cu:Zn ratio detected in UK Bangladeshis may therefore reflect early onset of disease process, and may ultimately result in these conditions for members of the Bangladeshi community.

[1]  P. Haris,et al.  The impact of a rice based diet on urinary arsenic. , 2011, Journal of environmental monitoring : JEM.

[2]  P. Haris,et al.  Betel quid chewing as a source of manganese exposure: total daily intake of manganese in a Bangladeshi population , 2011, BMC public health.

[3]  L. Knudsen,et al.  Exploring Exposure in 27 Countries in a European Human Biomonitoring Study—Cophes , 2011 .

[4]  P. Haris,et al.  Risk of human exposure to arsenic and other toxic elements from geophagy: trace element analysis of baked clay using inductively coupled plasma mass spectrometry , 2010, Environmental health : a global access science source.

[5]  Benoit Nemery,et al.  High human exposure to cobalt and other metals in Katanga, a mining area of the Democratic Republic of Congo. , 2009, Environmental research.

[6]  L. Rink,et al.  Zinc and diabetes--clinical links and molecular mechanisms. , 2009, The Journal of nutritional biochemistry.

[7]  R. Bhopal,et al.  Alcohol-related and hepatocellular cancer deaths by country of birth in England and Wales: analysis of mortality and census data. , 2009, Journal of public health.

[8]  M. Ramírez-Zea,et al.  Role of zinc in maternal and child mental health. , 2009, The American journal of clinical nutrition.

[9]  N. Nayak,et al.  Indian childhood cirrhosis: several dilemmas resolved. , 2008, The Indian journal of medical research.

[10]  M. Berglund,et al.  Urinary arsenic concentration adjustment factors and malnutrition. , 2008, Environmental research.

[11]  M. Vahter,et al.  Gender and age differences in the metabolism of inorganic arsenic in a highly exposed population in Bangladesh. , 2008, Environmental research.

[12]  T. Kazi,et al.  Copper, Chromium, Manganese, Iron, Nickel, and Zinc Levels in Biological Samples of Diabetes Mellitus Patients , 2008, Biological Trace Element Research.

[13]  J. Cocker,et al.  Background levels of key biomarkers of chemical exposure within the UK general population--pilot study. , 2007, International journal of hygiene and environmental health.

[14]  T. Okubo,et al.  Variation in the distribution of trace elements in hepatoma , 2003, Biological Trace Element Research.

[15]  P. Heitland,et al.  Biomonitoring of 30 trace elements in urine of children and adults by ICP-MS. , 2006, Clinica chimica acta; international journal of clinical chemistry.

[16]  D. Chakraborti,et al.  Pattern of Excretion of Arsenic Compounds [Arsenite, Arsenate, MMA(V), DMA(V)] in Urine of Children Compared to Adults from an Arsenic Exposed Area in Bangladesh , 2003, Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering.

[17]  H. Fukuda,et al.  A new diagnostic method for chronic hepatitis, liver cirrhosis, and hepatocellular carcinoma based on serum metallothionein, copper, and zinc levels. , 2002, Biological & pharmaceutical bulletin.

[18]  E. Ford Serum copper concentration and coronary heart disease among US adults. , 2000, American journal of epidemiology.

[19]  A. McMunn,et al.  Cardiovascular Disease Prevalence and Risk Factors , 2000 .

[20]  E. Sabbioni,et al.  Trace element reference values in tissues from inhabitants of the European Union. X. A study of 13 elements in blood and urine of a United Kingdom population. , 1998, The Science of the total environment.

[21]  P. Borella,et al.  Observations on the use of plasma, hair and tissue to evaluate trace element status in cancer. , 1997, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

[22]  R. G. Brown,et al.  Hyperzincuria in individuals with insulin-dependent diabetes mellitus: concurrent zinc status and the effect of high-dose zinc supplementation. , 1994, Metabolism: clinical and experimental.

[23]  I. Sternlieb,et al.  Is non-Indian childhood cirrhosis caused by excess dietary copper? , 1994, The Lancet.

[24]  Kenneth D. McClatchey,et al.  Clinical laboratory medicine , 1994 .

[25]  P Apostoli,et al.  Trace element reference values in tissues from inhabitants of the European community. I. A study of 46 elements in urine, blood and serum of Italian subjects. , 1990, The Science of the total environment.

[26]  X. Li,et al.  Studies of safe maximal daily dietary selenium intake in a seleniferous area in China. I. Selenium intake and tissue selenium levels of the inhabitants. , 1989, Journal of trace elements and electrolytes in health and disease.

[27]  B. Belohradsky,et al.  First Description of “Indian Childhood Cirrhosis” in a Non‐Indian Infant in Europe , 1989, Acta paediatrica Scandinavica.

[28]  C. Fleming,et al.  Zinc-induced copper deficiency. , 1988, Gastroenterology.

[29]  K. Hambidge,et al.  Zinc Nutriture in Type I Diabetes Mellitus: Relationship to Growth Measures and Metabolic Control , 1984, Journal of pediatric gastroenterology and nutrition.

[30]  G. Yang,et al.  Endemic selenium intoxication of humans in China. , 1983, The American journal of clinical nutrition.

[31]  Roger Williams,et al.  INCREASED HEPATIC COPPER CONCENTRATION IN INDIAN CHILDHOOD CIRRHOSIS , 1979, The Lancet.

[32]  A. Prasad,et al.  Hypocupremia induced by zinc therapy in adults. , 1978, JAMA.