A Delta-Aminolevulinic Acid Dehydratase (ALAD) Polymorphism May Modify the Relationship of Low-Level Lead Exposure to Uricemia and Renal Function: The Normative Aging Study

Details

• Personal Author:
  Hu H ; Kelsey K ; Schwartz J ; Sparrow D ; Weiss S ; Wu M-T
• Description:
  In this study we investigated whether a known delta-aminolevulinic acid dehydratase (ALAD) exon 4 polymorphism has a modifying effect on the association of blood or bone lead level with uricemia and indices of renal function among middle-aged and elderly men. We performed a cross-sectional study of subjects who participated between 1991 and 1995 in the Department of Veterans Affairs Normative Aging Study. Information on blood lead levels, bone lead levels (measured by K-shell X-ray fluorescence), serum uric acid, serum creatinine, estimated creatinine clearance, and ALAD polymorphism status was available in 709 subjects. Regression models were constructed to examine the relationships of serum uric acid, serum creatinine, and estimated creatinine clearance to blood or bone lead level, stratified by genotype. We also adjusted for age, body mass index, blood pressure, smoking, alcohol consumption, and ingestion of analgesic medications (n = 638). Of the 709 subjects, 7 (1%) and 107 (15%) were homozygous and heterozygous for the variant (ALAD-2) allele, respectively. The mean (range) serum uric acid and creatinine levels were 6.5 (2.9-10.6) and 1.2 (0.6-2.5) mg/dL. No significant differences were found in serum uric acid, serum creatinine, or estimated creatinine clearance by ALAD genotype. However, after adjusting for other potential confounders, we found a significant linear relationship between serum uric acid and patella bone lead (p = 0.040) among the ALAD 1-2/2-2 genotype individuals above a threshold patellar lead level of 15 micro g/g. In contrast, among the wild-type (ALAD 1-1) individuals, there was a suggestion of a significant linear relationship of serum uric acid with patella bone lead (p = 0.141), but only after a threshold of 101 micro g/g. There was evidence of a significant (p = 0.025) interaction of tibia lead with genotype (ALAD 1-1 vs. ALAD 1-2/2-2) regarding serum creatinine as an outcome, but in the same linear regression model tibia lead alone was not a significant predictor of serum creatinine. Conversely, for estimated creatinine clearance, patella lead, but not the interaction of patella lead with genotype, was a significantly independent predictor (p = 0.026). Our findings suggest that ALAD genotype may modify the effect of lead on the renal excretion of uric acid as well as overall renal function among middle-aged and elderly men who had community (nonoccupational) exposures to lead. Additional research is needed to ascertain whether this constitutes a true gene-environment interaction and, if so, its clinical impact. [Description provided by NIOSH]
• Subjects:
  Aging Alcoholic Beverages Blood Environmental Exposure Lead Men Occupational Health Safety Smokers Urine
• Keywords:
  Age Groups Alcohol Analgesics Author Keywords: ä-aminolevulinic Acid Dehydratase Blood Lead Levels Blood Pressure BMI Body Mass Index Bone Lead Bone Structure Chemicals Environmental Exposure Genotype Health Effects Humans Kidney Disorders Kidneys Lead Compounds Models Physiology Serum Creatinine Serum Uric Acid Smoking Urinalysis X-ray Fluorescence Analysis

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• ISSN:
  0091-6765
• Document Type:
  Text
• Funding:
  Grant
• Genre:
  Journal Article
• Place as Subject:
  Massachusetts ; OSHA Region 1
• CIO:
  National Institute for Occupational Safety and Health (NIOSH)
• Topic:
  Workplace Safety & Health
• Location:
  North America
• Pages in Document:
  335-341
• Volume:
  111
• Issue:
  3
• NIOSHTIC Number:
  nn:20059950
• Citation:
  Environ Health Perspect 2003 Mar; 111(3):335-341
• Contact Point Address:
  H. Hu, Channing Laboratory, Harvard Medical School, 181 Longwood Avenue, Boston, MA 02115
• Email:
  howard.hu@channing.harvard.edu
• CAS Registry Number:
  Lead (CAS RN 7439-92-1)
• Federal Fiscal Year:
  2003
• Performing Organization:
  Harvard School of Public Health
• Peer Reviewed:
  True
• Start Date:
  20030701
• Source Full Name:
  Environmental Health Perspectives
• End Date:
  20050630
• Collection(s):
  National Institute for Occupational Safety and Health
• Main Document Checksum:
  urn:sha-512:9e36cc54ff3cc1ae6f4b241b6320f2f8f9481046e8df37f7388cd8d9e0bacd032bf5a1618a3656ee454bc9a810a98c49f3c28208f8e9d371e35f596589222814
• Download URL:
  https://stacks.cdc.gov/view/cdc/224002/cdc_224002_DS1.pdf
• File Type:
  [PDF - 654.13 KB ]