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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2010-5-11
pubmed:abstractText
The authors conducted a 2003-2007 case-control study including 184 cases and 194 controls to examine the association between blood lead and the risk of amyotrophic lateral sclerosis (ALS) among US veterans and to explore the influence on this association of bone turnover and genetic factors related to lead toxicokinetics. Blood lead, plasma biomarkers of bone formation (procollagen type 1 amino-terminal peptide (PINP)) and resorption (C-terminal telopeptides of type 1 collagen (CTX)), and the K59N polymorphism in the delta-aminolevulinic acid dehydratase gene, ALAD, were measured. Odds ratios and 95% confidence intervals for the association of blood lead with ALS were estimated with unconditional logistic regression after adjustment for age and bone turnover. Blood lead levels were higher among cases compared with controls (P < 0.0001, age adjusted). A doubling of blood lead was associated with a 1.9-fold increased risk of ALS (95% confidence interval: 1.3, 2.7) after adjustment for age and CTX. Additional adjustment for PINP did not alter the results. Significant lead-ALS associations were observed in substrata of PINP and CTX levels. The K59N polymorphism in the ALAD gene did not modify the lead-ALS association (P = 0.32). These results extend earlier findings by accounting for bone turnover in confirming the association between elevated blood lead level and higher risk of ALS.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-10022280, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-10364720, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-10463764, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-10645818, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-10698721, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-11427399, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-11464847, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-11564619, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-11964933, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-12896855, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-14504315, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-14504316, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-1463680, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-15229114, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-15642900, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-15650320, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-16909025, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-16985039, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-17932355, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-18333495, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-18421218, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-18421219, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-19191304, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-2067636, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-3376124, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-3748267, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-3962963, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-5497881, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-7235610, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-8229031, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-8857824, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-9199537, http://linkedlifedata.com/resource/pubmed/commentcorrection/20406759-946326
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1476-6256
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
171
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1126-33
pubmed:dateRevised
2011-7-28
pubmed:meshHeading
pubmed-meshheading:20406759-Adult, pubmed-meshheading:20406759-Aged, pubmed-meshheading:20406759-Aged, 80 and over, pubmed-meshheading:20406759-Amyotrophic Lateral Sclerosis, pubmed-meshheading:20406759-Biological Markers, pubmed-meshheading:20406759-Bone Resorption, pubmed-meshheading:20406759-Bone and Bones, pubmed-meshheading:20406759-Case-Control Studies, pubmed-meshheading:20406759-Confidence Intervals, pubmed-meshheading:20406759-Environmental Exposure, pubmed-meshheading:20406759-Female, pubmed-meshheading:20406759-Humans, pubmed-meshheading:20406759-Lead, pubmed-meshheading:20406759-Lead Poisoning, pubmed-meshheading:20406759-Logistic Models, pubmed-meshheading:20406759-Male, pubmed-meshheading:20406759-Middle Aged, pubmed-meshheading:20406759-Odds Ratio, pubmed-meshheading:20406759-Osteogenesis, pubmed-meshheading:20406759-Porphobilinogen Synthase, pubmed-meshheading:20406759-Questionnaires, pubmed-meshheading:20406759-Registries, pubmed-meshheading:20406759-Risk Factors, pubmed-meshheading:20406759-United States, pubmed-meshheading:20406759-Veterans
pubmed:year
2010
pubmed:articleTitle
Association between blood lead and the risk of amyotrophic lateral sclerosis.
pubmed:affiliation
Epidemiology Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA.
pubmed:publicationType
Journal Article
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