Relationship between mercury in kidney, blood, and urine in environmentally exposed individuals, and implications for biomonitoring
(2017) In Toxicology and Applied Pharmacology 320. p.17-25- Abstract
Background Individuals without occupational exposure are exposed to mercury (Hg) from diet and dental amalgam. The kidney is a critical organ, but there is limited information regarding the relationship between Hg in kidney (K-Hg), urine (U-Hg), blood (B-Hg), and plasma (P-Hg). Objectives The aim was to determine the relationship between K-Hg, U-Hg, B-Hg, and P-Hg among environmentally exposed individuals, estimate the biological half-time of K-Hg, and provide information useful for biomonitoring of Hg. Methods Kidney cortex biopsies and urine and blood samples were collected from 109 living kidney donors. Total Hg concentrations were determined and the relationships between K-Hg, U-Hg, P-Hg, and B-Hg were investigated in regression... (More)
Background Individuals without occupational exposure are exposed to mercury (Hg) from diet and dental amalgam. The kidney is a critical organ, but there is limited information regarding the relationship between Hg in kidney (K-Hg), urine (U-Hg), blood (B-Hg), and plasma (P-Hg). Objectives The aim was to determine the relationship between K-Hg, U-Hg, B-Hg, and P-Hg among environmentally exposed individuals, estimate the biological half-time of K-Hg, and provide information useful for biomonitoring of Hg. Methods Kidney cortex biopsies and urine and blood samples were collected from 109 living kidney donors. Total Hg concentrations were determined and the relationships between K-Hg, U-Hg, P-Hg, and B-Hg were investigated in regression models. The half-time of K-Hg was estimated from the elimination constant. Results There were strong associations between K-Hg and all measures of U-Hg and P-Hg (rp = 0.65–0.84, p < 0.001), while the association with B-Hg was weaker (rp = 0.29, p = 0.002). Mean ratios between K-Hg (in μg/g) and U-Hg/24h (in μg) and B-Hg (in μg/L) were 0.22 and 0.19 respectively. Estimates of the biological half-time varied between 30 and 92 days, with significantly slower elimination in women. Adjusting overnight urine samples for dilution using urinary creatinine resulted in less bias in relation to K-Hg or U-Hg/24h, compared with other adjustment techniques. Conclusions The relationship between K-Hg and U-Hg is approximately linear. K-Hg can be estimated using U-Hg and gender. Women have longer half-time of Hg in kidney compared to men. Adjusting overnight urine samples for creatinine concentration resulted in less bias.
(Less)
- author
- Akerstrom, Magnus ; Barregard, Lars ; Lundh, Thomas LU and Sallsten, Gerd
- organization
- publishing date
- 2017-04-01
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Biomonitoring, Blood, Kidney, Mercury, Plasma, Urine
- in
- Toxicology and Applied Pharmacology
- volume
- 320
- pages
- 9 pages
- publisher
- Academic Press
- external identifiers
-
- scopus:85013157912
- pmid:28189652
- wos:000396798200003
- ISSN
- 0041-008X
- DOI
- 10.1016/j.taap.2017.02.007
- language
- English
- LU publication?
- yes
- id
- 4461d4db-d4dc-4adb-9617-a7ca7bdde48f
- date added to LUP
- 2017-03-01 08:40:18
- date last changed
- 2025-01-07 08:42:44
@article{4461d4db-d4dc-4adb-9617-a7ca7bdde48f, abstract = {{<p>Background Individuals without occupational exposure are exposed to mercury (Hg) from diet and dental amalgam. The kidney is a critical organ, but there is limited information regarding the relationship between Hg in kidney (K-Hg), urine (U-Hg), blood (B-Hg), and plasma (P-Hg). Objectives The aim was to determine the relationship between K-Hg, U-Hg, B-Hg, and P-Hg among environmentally exposed individuals, estimate the biological half-time of K-Hg, and provide information useful for biomonitoring of Hg. Methods Kidney cortex biopsies and urine and blood samples were collected from 109 living kidney donors. Total Hg concentrations were determined and the relationships between K-Hg, U-Hg, P-Hg, and B-Hg were investigated in regression models. The half-time of K-Hg was estimated from the elimination constant. Results There were strong associations between K-Hg and all measures of U-Hg and P-Hg (r<sub>p</sub> = 0.65–0.84, p < 0.001), while the association with B-Hg was weaker (r<sub>p</sub> = 0.29, p = 0.002). Mean ratios between K-Hg (in μg/g) and U-Hg/24h (in μg) and B-Hg (in μg/L) were 0.22 and 0.19 respectively. Estimates of the biological half-time varied between 30 and 92 days, with significantly slower elimination in women. Adjusting overnight urine samples for dilution using urinary creatinine resulted in less bias in relation to K-Hg or U-Hg/24h, compared with other adjustment techniques. Conclusions The relationship between K-Hg and U-Hg is approximately linear. K-Hg can be estimated using U-Hg and gender. Women have longer half-time of Hg in kidney compared to men. Adjusting overnight urine samples for creatinine concentration resulted in less bias.</p>}}, author = {{Akerstrom, Magnus and Barregard, Lars and Lundh, Thomas and Sallsten, Gerd}}, issn = {{0041-008X}}, keywords = {{Biomonitoring; Blood; Kidney; Mercury; Plasma; Urine}}, language = {{eng}}, month = {{04}}, pages = {{17--25}}, publisher = {{Academic Press}}, series = {{Toxicology and Applied Pharmacology}}, title = {{Relationship between mercury in kidney, blood, and urine in environmentally exposed individuals, and implications for biomonitoring}}, url = {{http://dx.doi.org/10.1016/j.taap.2017.02.007}}, doi = {{10.1016/j.taap.2017.02.007}}, volume = {{320}}, year = {{2017}}, }