Skip to main content

The toxicity of cadmium and resulting hazards for human health


Cadmium (Cd) has been in industrial use for a long period of time. Its serious toxicity moved into scientific focus during the middle of the last century. In this review, we discuss historic and recent developments of toxicological and epidemiological questions, including exposition sources, resorption pathways and organ damage processes.


Cadmium (group IIB of the periodic table of elements) is a heavy metal posing severe risks to human health. Up to this day, it could not be shown that cadmium has any physiological function within the human body. Interest has therefore risen in its biohazardous potential. As first described by Friedrich Stromeyer (Göttingen, Germany) in 1817, cadmium intoxication can lead to kidney, bone, and pulmonary damages.

In this article, we review recent developments and findings of cadmium toxicology.


Cadmium is regularly found in ores together with zinc, copper and lead. Therefore volcanic activity is one natural reason for a temporary increase in environmental cadmium concentrations. Cadmium is widely used in industrial processes, e.g.: as an anticorrosive agent, as a stabilizer in PVC products, as a colour pigment, a neutron-absorber in nuclear power plants, and in the fabrication of nickel-cadmium batteries. Phosphate fertilizers also show a big cadmium load. Although some cadmium-containing products can be recycled, a large share of the general cadmium pollution is caused by dumping and incinerating cadmium-polluted waste [1]. In Scandinavia for example, cadmium concentration in agricultural soil increases by 0.2% per year. Total global emission of cadmium amounts to 7000 t/year [2].

Resorption into human body

The maximum permissible value for workers according to German law is 15 μg/l. For comparison: Non-smokers show an average cadmium blood concentration of 0.5 μg/l.

Basically there are three possible ways of cadmium resorption: Gastrointestinal, pulmonary and dermal.

Digestive system

The uptake through the human gastrointestinal is approximately 5% of an ingested amount of cadmium, depending on the exact dose and nutritional composition [3]. An average German citizen has a daily intake of 30–35 μg cadmium; 95% of this taken up with food and drinks. An average smoker has an additional intake of 30 μg per day [4]. Several factors can increase this amount, such as low intakes of vitamin D, calcium, and trace elements like zinc and copper.

Concerning zinc and calcium, it is assumed that their molecular homology could be a reason for a compensatory higher cadmium resorption [5]. Foulkes was able to show such a competitive resorption of Cd in an animal model: In rat jejunum, the cadmium uptake was depressed by relatively high concentrations of other polyvalent cations, including Pb, Ni, Cr3+, Sr, and Mg [6].

Furthermore a high fiber diet increases the dietary cadmium intake [7]. The most important metabolic parameter for cadmium uptake is a person's possible lack of iron. People with low iron supplies showed a 6% higher uptake of cadmium than those with a balanced iron stock [8]. This is the main reason for the higher cadmium resorption in people with anaemia and habitual iron deficit, such as children or menstruating women. Low iron blood levels stimulate the expression of DCT-1, a metal ion transporter in the GI tract, serving as a gate for cadmium resorption [9].

Respiratory system

The major source of inhalative cadmium intoxication is cigarette smoke. The human lung resorbes 40–60% of the cadmium in tobacco smoke [10]. A 50 year-old average non-smoker has a cadmium body burden of 15 mg. While a comparable life-long smoker shows a value of 30 mg. Smokers generally have cadmium blood levels 4–5 times those of non-smokers [7].

Workers exposed to cadmium-containing fumes have been reported to develop acute respiratory distress syndromes (ARDS) [11].

Inhalativly resorbed cadmium reaches blood circulation usually in form of cadmium-cysteine complexes [12].

Dermal resorption

Little research has been done on dermal absorption of cadmium. In 1991, Wester et al. experimented on the resorption from cadmium-contaminated soil and water solutions by human cadaver skin in a diffusion cell-model. They could demonstrate a penetration of 8.8 % (soil) and 12.7% (water) of the applied cadmium dose into the skin; while the plasma uptake from soil was 0.01% and 0.07% from water [13]. Lansdown and Sampson administered a cadmium chloride solution to the dorsum of rats (shaved skin) daily for 10 days. The skin showed hyperkeratosis and acanthosis with occasional ulcerative change, and an increase of the mitotic index of the skin cells. Also cadmium concentration in blood, liver and kidney increased, thus indicating percutaneous absorption [14].

Two mechanisms facilitate cadmium absorption by the skin: binding of a free cadmium ion to sulfhydryl radicals of cysteine in epidermal keratins, or an induction and complexing with metallothionein [15].

Handling Of cadmium in the body

Once taken up by the blood, the majority of cadmium is transported bound to proteins, such as Albumin and Metallothionein.

The first organ reached after uptake into the GI-blood is the liver. Here cadmium induces the production of Metallothionein. After consecutive hepatocyte necrosis and apoptosis, Cd-Metallothionein complexes are washed into sinusoidal blood. From here, parts of the absorbed cadmium enter the entero-hepatical cycle via secretion into the biliary tract in form of Cadmium-Glutathione conjugates. Enzymatically degraded to cadmium-cysteine complexes in the biliary tree, cadmium re-enters the small intestines [12].

The main organ for long-term cadmium accumulation is the kidney [16]. Here the half-life period for cadmium is approx. 10 years. A life-long intake can therefore lead to a cadmium accumulation in the kidney, consequently resulting in tubulus cell necrosis.

The blood concentration of cadmium serves as a reliable indicator for a recent exposition, while the urinary concentration reflects past exposure, body burden and renal accumulation [3]. Excretion of Cadmium takes place via faeces and urine. Figure 1 gives a scheme on the handling of Cadmium in human body.

Figure 1
figure 1

Handling of cadmium in human body. Figure legend text: Metabolism, storage and excretion of cadmium in human body. Modified after [12].

Hazards to human health

Acute intoxication

The respiratory system is affected severely by the inhalation of cadmium-contaminated air: Shortness of breath, lung edema and destruction of mucous membranes as part of cadmium-induced pneumonitis are described [17]. As already reported in 1942, intake of cadmium-contaminated food causes acute gastrointestinal effects, such as vomiting and diarrhoea [18].

Kidney damage

Kidney damage has long since been described to be the main problem for patients chronically exposed to cadmium [19]. As mentioned above, cadmium reaches the kidney in form of cadmium-metallothionein (Cd-MT). Cd-MT is filtrated in the glomerulus, and subsequently reabsorbed in the proximal tubulus. It then remains in the tubulus cells and makes up for the major part of the cadmium body burden. The amount of cadmium in the kidney tubulus cells increases during every person's life span. A perturbance of the phosphor and calcium metabolism as a result of this phenomenon is in discussion [20]. An increasing cadmium load in the kidney is also discussed to result in a higher calcium excretion, thus leading to a higher risk of kidney stones.

The urinary cadmium excretion was shown to correlate with the degree of cadmium induced kidney damage: A urinary excretion of 2.5 micrograms cadmium per gram creatinine reflects a renal tubular damage degree of 4% [7]. The primary markers of kidney damage however, are the urinarily excreted β2-microglobulin, N-acetyl-α-D-glucosaminidase (NAG), and retinol-binding-protein (RBP) [21]. The ChinaCad-Study showed significantly higher values for urinary β2-Microglobulin and RBP in people with high blood cadmium concentration than in people with normal values [3]. In the first group, both glomerular and tubular damages where observed. It has been discussed whether or not tubular damage is reversible [22]. The general opinion today however is, that it's irreversible.

Effects of cadmium in reproductive biology

Cadmium appears to interfere with the ovarian steroidogenic pathway in rats. Piasek et al. evaluated the direct effects of in vitro cadmium exposure on steroidogenesis in rat ovaries.

The most affected were productions of progesterone and testosterone [23]. Low dosages of cadmium are reported to stimulate ovarian progesterone biosynthesis, while high dosages inhibit it [24]. Maternal exposure to cadmium is associated with low birth wight and an increase of spontaneous abortion [25, 26]. Some evidence exists also that cadmium is a potent nonsteroidal estrogen in vivo and in vitro. Studies in rats showed that cadmium precipitates enhanced mammary development and increased uterine wight [27].

Bone damage and the Itai-Itai-disease

Several studies in the 20th Century showed a connection between cadmium intoxication and bone damage, e.g. in workers exposed to cadmium-polluted fume and dust [28].

Cadmium could also be shown to be associated with occurrences of Itai-Itai, a disease under witch patients show a wide range of symptoms such as: low grade of bone mineralization, high rate of fractures, increased rate of osteoporosis, and intense bone associated pain. An epidemic occurrence of the Itai-Itai disease was observed in the Jinzu river basin (Japan) in the 1940s. In a study on this occasion, patients where found to show the characteristic symptoms after having eaten rice, grown on fields irrigated with highly cadmium polluted water. Also pseudo fractures characteristic of osteomalacia and severe skeletal decalcification could be observed. Criticism of this study came up because of the fact that the majority of the patient collective was made up of women in the post-menopause [29]. Underlying osteoporosis, possibly enhanced by cadmium intoxication, was suggested to be the actual reason for the observed symptoms [30].

Further evidence for the causality of cadmium intoxication for bone maladies was found in 2003 by Honda et al. They could describe an inverse correlation of the STIFF index (an ultrasound method for measuring bone density) and urine cadmium concentration [25]. Similar findings where made within the OSCAR-Study, conducted with 1021 people from southern Sweden. Here a significant negative correlation could be shown between urine cadmium concentration and low bone mineral density; especially in people of an age of 60 years and above. Furthermore evidence for an increased risk of forearm fractures in cadmium-exposed individuals was found [31]. Individuals included in this study were either battery plant workers, or inhabitants of a town close to the battery plant. A collective of unexposed people where included as reference group.

The Belgian CadmiBel study – conducted between 1985 and 1989 – came to similar conclusions: Even minimal environmental exposure to cadmium is supposed to cause skeletal demineralisation [32]. Some of the CadmiBel-participants were later tested for forearm bone density during the so called PheeCad Study (1992–1995). Here too lower bone densities where found in individuals previously exposed to cadmium. The most interesting aspect of this study was the fact, that their total cadmium body burden (according to the urinary cadmium excretion) was significantly lower than that of Japanese Itai-Itai patients: CadmiBel/PheeCad participants showed a urinary cadmium excretion of only 1 μg/g creatinine, while Itai-Itai patients where found to have an excretion of approximately 30 μg/g creatinine.

The exact mechanism of interference between cadmium and bone mineralization remains to be discovered. Presently, a direct influence on osteoblast and osteoclast function seems as likely as an indirect influence via induction of renal dysfunction [33]. A perturbance of the vitamin D3 metabolic pathway through cadmium is also in discussion: According to these hypothesises, lead and cadmium interact with renal mitochondrial hydroxylases of the vitamin D3 endocrine complex [34]. Figure 2 gives an overview on the effects of cadmium in several organ systems.

Figure 2
figure 2

Effects of cadmium on several organ systems.


There is some proof that cadmium can cause cancer. Waalkes et al. have shown that a subcutaneous injection of cadmium chloride can induce prostate cancer in Wistar rats [35]. This group also postulated that high doses of cadmium can cause severe testicular necrosis in rats, followed by a higher incidence of testicular interstitial tumors. In contrast to laboratory data though, epidemiological studies could not convincingly prove cadmium to be a cause of prostate cancer [36].

Early publications however suggested an association of cadmium and renal cancer in humans [37]. This assumption was confirmed in 2005 by a systematic review of seven epidemiological and eleven clinical studies [38]. Consequently, the IARC (International Agency for Research on Cancer) decided to classify cadmium as a human carcinogen group I. Latest data however supports the assumption that only an uptake of cadmium via the respiratory system has carcinogenic potential [3].

Although molecular mechanisms of cadmium-induced carcinogenesis are not yet understood, several factors may contribute to it: Up-regulation of mitogenic signalling, perturbance of DNA-repairing mechanism, and acquisition of apoptotic resistance by cadmium exposure [39]. A substitution of zinc by cadmium in transcription-regulating proteins is also in discussion. Furthermore, new data showed that cadmium is able to change the conformation of E-Cadherin, a transmembrane Ca(II)-binding glycoprotein. E-Cadherin plays an important role in cell-cell adhesions, especially in epidermal cells [40]. These results are consistent with the hypothesis that E-cadherin may be a direct molecular target for Cd(2+) toxicity.

There are many further fields of occupational medicine and toxicology in which cadmium is currently suspected to play a major role [4145] They are omitted with regard to the limited space and the comprehensiveness of this review.


Latest studies have proven the importance of a reduction of cadmium emissions for human health. Some efforts in this direction have been made, especially within in the European Union. Cadmium, on the one hand, is example for an industrially used substance with negative long-time effects on human health. On the other hand, it is an example for the beneficial potential of the international cooperation of laboratories, universities and local authorities. Efforts to research and reduce the effects of cadmium emissions have to continue. A number of promising projects give rise to the hope that, in the future, alternative testing methods may allow a reduction of the number of laboratory animals necessary for this research.

Table 1 Recent studys on Cadmium toxicity


  1. Jarup L: Hazards of heavy metal contamination. Br Med Bull 2003, 68: 167–182. 10.1093/bmb/ldg032

    Article  PubMed  Google Scholar 

  2. Stoeppler: Cadmium. In Metals and their compounds in the environment. Edited by: E M. Weinheim , Verlag Chemie; 1991:805–849.

    Google Scholar 

  3. Jin T, Nordberg M, Frech W, Dumont X, Bernard A, Ye TT, Kong Q, Wang Z, Li P, Lundstrom NG, Li Y, Nordberg GF: Cadmium biomonitoring and renal dysfunction among a population environmentally exposed to cadmium from smelting in China (ChinaCad). Biometals 2002,15(4):397–410. 10.1023/A:1020229923095

    Article  CAS  PubMed  Google Scholar 

  4. Schwarz E CMKC: Cadmium. Umwelt-Survey. WaBoLuHefte 1993., 2:

    Google Scholar 

  5. Taylor WR: Permeation of barium and cadmium through slowly inactivating calcium channels in cat sensory neurones. J Physiol 1988, 407: 433–452.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  6. Foulkes EC: Interactions between metals in rat jejunum: implications on the nature of cadmium uptake. Toxicology 1985,37(1–2):117–125. 10.1016/0300-483X(85)90118-0

    Article  CAS  PubMed  Google Scholar 

  7. Jarup L, Berglund M, Elinder CG, Nordberg G, Vahter M: Health effects of cadmium exposure--a review of the literature and a risk estimate. Scand J Work Environ Health 1998, 24 Suppl 1: 1–51.

    CAS  PubMed  Google Scholar 

  8. Flanagan PR, McLellan JS, Haist J, Cherian G, Chamberlain MJ, Valberg LS: Increased dietary cadmium absorption in mice and human subjects with iron deficiency. Gastroenterology 1978,74(5 Pt 1):841–846.

    CAS  PubMed  Google Scholar 

  9. Gunshin H, Mackenzie B, Berger UV, Gunshin Y, Romero MF, Boron WF, Nussberger S, Gollan JL, Hediger MA: Cloning and characterization of a mammalian proton-coupled metal-ion transporter. Nature 1997,388(6641):482–488. 10.1038/41343

    Article  CAS  PubMed  Google Scholar 

  10. Elinder CG, Lind B, Kjellstrom T, Linnman L, Friberg L: Cadmium in kidney cortex, liver, and pancreas from Swedish autopsies. Estimation of biological half time in kidney cortex, considering calorie intake and smoking habits. Arch Environ Health 1976,31(6):292–302.

    Article  CAS  PubMed  Google Scholar 

  11. Barbee JYJ, Prince TS: Acute respiratory distress syndrome in a welder exposed to metal fumes. South Med J 1999,92(5):510–512.

    Article  PubMed  Google Scholar 

  12. Zalups RK AS: Molecular handling of cadmium in transporting epithelia. Toxicol Appl Pharmacol 2003,186(3):163–188. 10.1016/S0041-008X(02)00021-2

    Article  PubMed  Google Scholar 

  13. Wester RC, Maibach HI, Sedik L, Melendres J, DiZio S, Wade M: In vitro percutaneous absorption of cadmium from water and soil into human skin. Fundam Appl Toxicol 1992,19(1):1–5. 10.1016/0272-0590(92)90021-9

    Article  CAS  PubMed  Google Scholar 

  14. Lansdown AB, Sampson B: Dermal toxicity and percutaneous absorption of cadmium in rats and mice. Lab Anim Sci 1996,46(5):549–554.

    CAS  PubMed  Google Scholar 

  15. Fasanya-Odewumi C, Latinwo LM, Ikediobi CO, Gilliard L, Sponholtz G, Nwoga J, Stino F, Hamilton N, Erdos GW: The genotoxicity and cytotoxicity of dermally-administered cadmium: effects of dermal cadmium administration. Int J Mol Med 1998,1(6):1001–1006.

    CAS  PubMed  Google Scholar 

  16. Orlowski C, Piotrowski JK: Biological levels of cadmium and zinc in the small intestine of non-occupationally exposed human subjects. Hum Exp Toxicol 2003,22(2):57–63. 10.1191/0960327103ht326oa

    Article  CAS  PubMed  Google Scholar 

  17. Seidal K, Jorgensen N, Elinder CG, Sjogren B, Vahter M: Fatal cadmium-induced pneumonitis. Scand J Work Environ Health 1993,19(6):429–431.

    Article  CAS  PubMed  Google Scholar 

  18. Nordberg GF: Cadmium and health in the 21st century--historical remarks and trends for the future. Biometals 2004,17(5):485–489. 10.1023/B:BIOM.0000045726.75367.85

    Article  CAS  PubMed  Google Scholar 

  19. Barbier O, Jacquillet G, Tauc M, Cougnon M, Poujeol P: Effect of heavy metals on, and handling by, the kidney. Nephron Physiol 2005,99(4):p105–10. 10.1159/000083981

    Article  CAS  PubMed  Google Scholar 

  20. Svartengren M, Elinder CG, Friberg L, Lind B: Distribution and concentration of cadmium in human kidney. Environ Res 1986,39(1):1–7. 10.1016/S0013-9351(86)80002-0

    Article  CAS  PubMed  Google Scholar 

  21. Bernard A: Renal dysfunction induced by cadmium: biomarkers of critical effects. Biometals 2004,17(5):519–523. 10.1023/B:BIOM.0000045731.75602.b9

    Article  CAS  PubMed  Google Scholar 

  22. Hotz P, Buchet JP, Bernard A, Lison D, Lauwerys R: Renal effects of low-level environmental cadmium exposure: 5-year follow-up of a subcohort from the Cadmibel study. Lancet 1999,354(9189):1508–1513. 10.1016/S0140-6736(99)91145-5

    Article  CAS  PubMed  Google Scholar 

  23. Piasek M, Laskey JW: Effects of in vitro cadmium exposure on ovarian steroidogenesis in rats. J Appl Toxicol 1999,19(3):211–217. 10.1002/(SICI)1099-1263(199905/06)19:3<211::AID-JAT568>3.0.CO;2-4

    Article  CAS  PubMed  Google Scholar 

  24. Henson MC, Chedrese PJ: Endocrine disruption by cadmium, a common environmental toxicant with paradoxical effects on reproduction. Exp Biol Med (Maywood) 2004,229(5):383–392.

    CAS  Google Scholar 

  25. Frery N, Nessmann C, Girard F, Lafond J, Moreau T, Blot P, Lellouch J, Huel G: Environmental exposure to cadmium and human birthweight. Toxicology 1993,79(2):109–118. 10.1016/0300-483X(93)90124-B

    Article  CAS  PubMed  Google Scholar 

  26. Shiverick KT, Salafia C: Cigarette smoking and pregnancy I: ovarian, uterine and placental effects. Placenta 1999, 20: 265–272. 10.1053/plac.1998.0377

    Article  CAS  PubMed  Google Scholar 

  27. Johnson MD, Kenney N, Stoica A, Hilakivi-Clarke L, Singh B, Chepko G, Clarke R, Sholler PF, Lirio AA, Foss C, Reiter R, Trock B, Paik S, Martin MB: Cadmium mimics the in vivo effects of estrogen in the uterus and mammary gland. Nat Med 2003,9 (8):1081–1084. 10.1038/nm902

    Article  CAS  PubMed  Google Scholar 

  28. Kazantzis G: Renal tubular dysfunction and abnormalities of calcium metabolism in cadmium workers. Environ Health Perspect 1979, 28: 155–159.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  29. Nogawa K, Kobayashi E, Okubo Y, Suwazono Y: Environmental cadmium exposure, adverse effects and preventive measures in Japan. Biometals 2004,17(5):581–587. 10.1023/B:BIOM.0000045742.81440.9c

    Article  CAS  PubMed  Google Scholar 

  30. Kazantzis G: Cadmium, osteoporosis and calcium metabolism. Biometals 2004,17(5):493–498. 10.1023/B:BIOM.0000045727.76054.f3

    Article  CAS  PubMed  Google Scholar 

  31. Jarup L, Alfven T, Persson B, Toss G, Elinder CG: Cadmium may be a risk factor for osteoporosis. Occup Environ Med 1998,55(7):435–439.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  32. Staessen JA, Roels HA, Emelianov D, Kuznetsova T, Thijs L, Vangronsveld J, Fagard R: Environmental exposure to cadmium, forearm bone density, and risk of fractures: prospective population study. Public Health and Environmental Exposure to Cadmium (PheeCad) Study Group. Lancet 1999,353(9159):1140–1144. 10.1016/S0140-6736(98)09356-8

    Article  CAS  PubMed  Google Scholar 

  33. Berglund M, Akesson A, Bjellerup P, Vahter M: Metal-bone interactions. Toxicol Lett 2000, 112–113: 219–225. 10.1016/S0378-4274(99)00272-6

    Article  CAS  PubMed  Google Scholar 

  34. Chalkley SR, Richmond J, Barltrop D: Measurement of vitamin D3 metabolites in smelter workers exposed to lead and cadmium. Occup Environ Med 1998,55(7):446–452.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  35. Waalkes MP, Rehm S, Riggs CW, Bare RM, Devor DE, Poirier LA, Wenk ML, Henneman JR, Balaschak MS: Cadmium carcinogenesis in male Wistar [Crl:(WI)BR] rats: dose-response analysis of tumor induction in the prostate and testes and at the injection site. Cancer Res 1988,48(16):4656–4663.

    CAS  PubMed  Google Scholar 

  36. Sahmoun AE, Case LD, Jackson SA, Schwartz GG: Cadmium and prostate cancer: a critical epidemiologic analysis. Cancer Invest 2005,23(3):256–263.

    Article  CAS  PubMed  Google Scholar 

  37. Kolonel LN: Association of cadmium with renal cancer. Cancer 1976,37(4):1782–1787. 10.1002/1097-0142(197604)37:4<1782::AID-CNCR2820370424>3.0.CO;2-F

    Article  CAS  PubMed  Google Scholar 

  38. Il'yasova D SGG: Cadmium and renal cancer. Toxicol Appl Pharmacol 2005,207(2):179–186. 10.1016/j.taap.2004.12.005

    Article  PubMed  Google Scholar 

  39. Goyer RA, Liu J, Waalkes MP: Cadmium and cancer of prostate and testis. Biometals 2004,17(5):555–558. 10.1023/B:BIOM.0000045738.59708.20

    Article  CAS  PubMed  Google Scholar 

  40. Prozialeck WC, Lamar PC: Interaction of cadmium (Cd(2+)) with a 13-residue polypeptide analog of a putative calcium-binding motif of E-cadherin. Biochim Biophys Acta 1999,1451(1):93–100. 10.1016/S0167-4889(99)00077-4

    Article  CAS  PubMed  Google Scholar 

  41. Groneberg DA, Nowak D, Wussow A, Fischer A: Chronic cough due to occupational factors. J Occup Med Toxicol1 2005.,1(3):

    Google Scholar 

  42. Groneberg DA, Kraus T, Fischer A: Chronic cough: tobacco smoke, particulate matter, ozone, nitrogen oxides and other environmental factors. J Occup Med Toxicol 2005.,1(4):

    Google Scholar 

  43. Wagner U, Staats P, HC Fehmann HC, Fischer AG, Groneberg DA: Functional airway secretion in a rat model of sulfur dioxide induced chronic obstructive pulmonary disease (COPD) . J Occup Med Toxicol 2005.,1(5):

    Google Scholar 

  44. Dalvie MA, Myers JE: The relationship between reproductive outcome measures in DDT exposed malaria vector control workers: a cross-sectional study. J Occup Med Toxicol 2005.,1(6):

    Google Scholar 

  45. Yelin E, Katz P, Balmes J, Trupin L, Earnest G, Eisner M, Blanc P: Work Life of Persons with Asthma, Rhinitis, and COPD: A Study Using a National, Population-Based Sample. J Occup Med Toxicol 2005.,1(2):

    Google Scholar 

Download references

Author information

Authors and Affiliations


Corresponding author

Correspondence to Johannes Godt.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Godt, J., Scheidig, F., Grosse-Siestrup, C. et al. The toxicity of cadmium and resulting hazards for human health. J Occup Med Toxicol 1, 22 (2006).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: