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. (Environmental Medicine).In this study we investigated whether a known [delta]-aminolevulinic acid dehydratase dehydratase /de·hy·dra·tase/ (de-hi´drah-tas) a common name for a hydro-lyase.
n. (ALAD ALAD
d-aminolevulinic acid dehydratase. ) exon Exon
In split genes, a portion that is included in the ribonucleic acid (RNA) transcript of a gene and survives processing of the RNA in the cell nucleus to become part of a spliced messenger RNA (mRNA) or structural RNA in the cell cytoplasm. 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 cross-sectional study
See synchronic study.
n the scientific method for the analysis of data gathered from two or more samples at one point in time. 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 uric acid (yr`ĭk), white, odorless, tasteless crystalline substance formed as a result of purine degradation in man, other primates, dalmatians, birds, snakes, and lizards. , serum creatinine, estimated creatinine clearance creatinine clearance
The volume of serum or plasma that would be cleared of creatinine by one minute's excretion of urine.
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 stratified /strat·i·fied/ (strat´i-fid) formed or arranged in layers.
Arranged in the form of layers or strata. by genotype. We also adjusted for age, body mass index, blood pressure, smoking, alcohol consumption, and ingestion ingestion /in·ges·tion/ (-chun) the taking of food, drugs, etc., into the body by mouth.
1. The act of taking food and drink into the body by the mouth.
2. of analgesic analgesic (ăn'əljē`zĭk), any of a diverse group of drugs used to relieve pain. Analgesic drugs include the nonsteroidal anti-inflammatory drugs (NSAIDs) such as the salicylates, narcotic drugs such as morphine, and synthetic drugs medications (n = 638). Of the 709 subjects, 7 (1%) and 107 (15%) were homozygous ho·mo·zy·gous
Having the same alleles at one or more gene loci on homologous chromosome segments.
Identical genes controlling a specified inherited trait. and heterozygous het·er·o·zy·gous
1. Having different alleles at one or more corresponding chromosomal loci.
2. Of or relating to a heterozygote. for the variant (ALAD-2) allele allele (əlēl`): see genetics.
Any one of two or more alternative forms of a gene that may occur alternatively at a given site on a chromosome. , 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 patella (pətĕl`ə): see kneecap. bone lead (p = 0.040) among the ALAD 1-2/2-2 genotype individuals above a threshold patellar patellar
of or pertaining to the patella.
a cartilaginous process borne on the medial side of the patella of horses and cattle. 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 tibia: see leg. lead with genotype (ALAD 1-1 vs. ALAD 1-2/2-2) regarding serum creatinine as an outcome, but in the same linear regression Linear regression
A statistical technique for fitting a straight line to a set of data points. 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. Key words: [delta]-aminolevulinic acid dehydratase, bone lead, serum creatinine, serum uric acid. Environ Health Perspect 111:335-340 (2003). doi:10.1289/ehp.5504 available via http://dx.doi.org/[Online 31 October 2002]
Chronic community and occupational exposures of adults to lead have been associated with deleterious effects on multiple organ systems, with consequent impacts on health, such as renal function impairment, hyperuricemia hyperuricemia /hy·per·uri·ce·mia/ (-u?ri-se´me-ah) uricemia; an excess of uric acid in the blood.hyperurice´mic
An unusually high concentration of uric acid in the blood. , and hypertension (1,2). Recently, attention has focused on understanding genetic factors that explain differences in symptoms between individuals who have had similar lead exposures. Identification of such genes would presumably pre·sum·a·ble
That can be presumed or taken for granted; reasonable as a supposition: presumable causes of the disaster. help explain variation in the relationship between biologic markers of lead exposure and measures of organ dysfunction.
One genetic polymorphism that has been suggested (3) as a modifier (programming) modifier - An operation that alters the state of an object. Modifiers often have names that begin with "set" and corresponding selector functions whose names begin with "get". of the pharmacokinetic distribution of lead (and therefore its toxicity) concerns the alleles that code for the production of [delta]-aminolevulinic acid dehydratase (ALAD), which is the second enzyme in the biosynthetic bi·o·syn·the·sis
Formation of a chemical compound by a living organism. Also called biogenesis.
bi pathway of heine (4,5). In 1981, Battistuzzi et al. (5) showed that human ALAD protein is a polymorphic enzyme. Subsequently, Wetmur et al. (6) found that this enzyme is polymorphic because of a G-to-C transversion trans·ver·sion
Eruption of a tooth in a position normally occupied by another.
n eruption of a tooth in the wrong position of nucleotide 177 in a coding region that results in replacement of the amino acid amino acid (əmē`nō), any one of a class of simple organic compounds containing carbon, hydrogen, oxygen, nitrogen, and in certain cases sulfur. These compounds are the building blocks of proteins. lysine lysine (lī`sēn), organic compound, one of the 20 amino acids commonly found in animal proteins. Only the l-stereoisomer appears in mammalian protein. with asparginine. Although no significant difference was noted in the activities of the erythrocyte erythrocyte (ĭrĭth`rəsīt'): see blood.
or red blood cell or red blood corpuscle
Blood cell that carries oxygen from the lungs to the body tissues. ALAD 1-1, ALAD 1-2, or ALAD 2-2 (5), Bergdahl et al. (3) reported that the ALAD-2 subunit binds lead more tightly than does ALAD-1 subunit in vitro in vitro /in vi·tro/ (in ve´tro) [L.] within a glass; observable in a test tube; in an artificial environment.
In an artificial environment outside a living organism. .
Epidemiological studies have suggested that among lead-exposed workers and environmentally exposed children (7-9), individuals with either the ALAD 1-2 or 2-2 genotype had blood lead levels that were significantly higher than those of individuals with the ALAD 1-1 genotype. These findings suggest that the ALAD-2 polypeptide polypeptide: see peptide. binds lead more tightly and effectively than does ALAD-1.
Recently, two occupational epidemiologic studies in 691 members of a construction union and 89 lead-smelter workers have indicated that ALAD genotype may modify the effect of lead on uricemia and kidney dysfunction (10,11). In this study, we attempted to investigate the impact of ALAD polymorphism on the relationship of lead levels in both blood and bone to uricemia and kidney dysfunction among environmentally exposed men. Our a priori a priori
In epistemology, knowledge that is independent of all particular experiences, as opposed to a posteriori (or empirical) knowledge, which derives from experience. hypothesis was that our lead biomarkers would be independently correlated with hyperuricemia and renal dysfunction and that the ALAD variant type would modify this effect, particularly when blood lead or bone lead levels are high (12,13).
Participants. The Normative Aging Study (NAS (1) See network access server.
(2) (Network Attached Storage) A specialized file server that connects to the network. A NAS device contains a slimmed-down operating system and a file system and processes only I/O requests by supporting the popular ) is a longitudinal study longitudinal study
a chronological study in epidemiology which attempts to establish a relationship between an antecedent cause and a subsequent effect. See also cohort study. of aging established by the Veterans Administration in 1963 (14). Healthy male volunteers from the Greater Boston, Massachusetts, area were screened at entry and accepted into the study if they had no history of heart disease, hypertension, diabetes mellitus diabetes mellitus
Disorder of insufficient production of or reduced sensitivity to insulin. Insulin, synthesized in the islets of Langerhans (see Langerhans, islets of), is necessary to metabolize glucose. In diabetes, blood sugar levels increase (hyperglycemia). , cancer, peptic ulcer peptic ulcer: see ulcer.
Sore that develops in the mucous membrane of the stomach (more frequent in women) or duodenum (accounting for 80% of ulcers and more frequent in men) when its ability to resist acid in gastric juice is reduced. , gout gout, condition that manifests itself as recurrent attacks of acute arthritis, which may become chronic and deforming. It results from deposits of uric acid crystals in connective tissue or joints. , recurrent asthma, bronchitis, or sinusitis sinusitis
Inflammation of the sinuses. Acute sinusitis, usually due to infections such as the common cold, causes localized pain and tenderness, nasal obstruction and discharge, and malaise. . Men with either systolic blood pressure Systolic blood pressure
Blood pressure when the heart contracts (beats).
Mentioned in: Hypertension > 140 mm Hg or diastolic blood pressure Diastolic blood pressure
Blood pressure when the heart is resting between beats.
Mentioned in: Hypertension > 90 mm Hg at entry were disqualified. Between 1963 and 1968, a total of 2,280 men who met the entry criteria were enrolled, ranging in age from 21 to 80 years, with a mean age of 42 years at entry. Study participants were asked to return for examinations every 3-5 years. At each visit, extensive physical examination, laboratory, anthropometric an·thro·pom·e·try
The study of human body measurement for use in anthropological classification and comparison.
an , and questionnaire data were collected. Beginning in 1991, during the course of each continuing participant's regularly scheduled evaluation at the Department of Veterans Affairs outpatient clinic in Boston, a fresh blood specimen was obtained for measurement of lead and other biochemical indicators such as uric acid and serum creatinine after an overnight fast and abstinence from smoking, and permission was sought to take bone lead measurements by K-shell X-ray fluorescence (KXRF). Consenting individuals reported to the outpatient Clinical Research Center of the Brigham and Women's Hospital Brigham and Women's Hospital (BWH) is a hospital in the Longwood Area of the Boston, Massachusetts neighborhood of Mission Hill. With Massachusetts General Hospital, it is one of the two founding members of Partners HealthCare. in Boston. This study was approved by the Human Subjects Committees of the Brigham and Women's Hospital and the Harvard School of Public Health The Harvard School of Public Health is (colloquially, HSPH) is one of the professional graduate schools of Harvard University. Located in Longwood Area of the Boston, Massachusetts neighborhood of Mission Hill, next to Harvard Medical School and Cambridge, Massachusetts, .
Uric acid and renal function. Serum uric acid levels were measured by the colorimetric col·or·im·e·ter
1. Any of various instruments used to determine or specify colors, as by comparison with spectroscopic or visual standards.
2. phosphotungstic method (N-30) with the Technicon Autoanalyzer (Technicon Instruments, Tarrytown, NY, USA) (15). The assay included standards from the College of American Pathologists This article or section needs sources or references that appear in reliable, third-party publications. Alone, primary sources and sources affiliated with the subject of this article are not sufficient for an accurate encyclopedia article. . In addition, the correlation between the NAS colorimetric phosphotungstic method and the more specific urease urease /ure·ase/ (u´re-as) an enzyme that catalyzes the hydrolysis of urea to ammonia and carbon dioxide; it is a nickel protein of microorganisms and plants that is used in clinical assays of plasma urea concentrations. method at the clinical laboratory of the Massachusetts General Hospital Massachusetts General Hospital Health care The major teaching hospital for Harvard Medical School, widely regarded as one of the best health care centers in the world in 23 split serum samples was 0.93, indicating that these two methods are comparable (15,16).
Serum creatinine was measured by an Astra 8 analyzer (Beckman Instruments, Inc., Fullerton, CA, USA) (17). Creatinine clearance was estimated on the basis of the serum creatinine concentration according to the method of Cockcroft and Gault n. 1. (Geol.) A series of beds of clay and marl in the South of England, between the upper and lower greensand of the Cretaceous period. (18). The following formula predicts creatinine clearance from serum creatinine:
Creatinine clearance = (140 - age)x weight (kg)/ 72 x serum creatinine ([micro]g / dL)
Derivation included the relation between age and 24-hr creatinine excretion per kilogram of body weight (19).
Blood and bone lead measurements. Blood lead was measured by ESA 1. (architecture) ESA - Enterprise Systems Architecture.
2. (body) ESA - European Space Agency. Laboratories, Inc. (Chelmsford, MA, USA) (20). In tests on reference samples from the U.S. Centers for Disease Control and Prevention Centers for Disease Control and Prevention (CDC), agency of the U.S. Public Health Service since 1973, with headquarters in Atlanta; it was established in 1946 as the Communicable Disease Center. , precision (coefficient of variation Coefficient of Variation
A measure of investment risk that defines risk as the standard deviation per unit of expected return. ) ranged from 8% for concentrations below 30 [micro]g/dL to 1% for higher concentrations. Measurements below a concentration of lowest detection limit (1.0 [micro]g/dL) were coded at 0.5 [micro]g/dL (seven study subjects).
Bone lead measurements were taken of each subject's mid-tibia shaft and patella using an ABIOMED KXRF instrument (ABIO-MED, Inc., Danvers, MA, USA). The physical principles, technical specifications, validation, and quality control procedures of this instrument have been described in detail elsewhere (20,21). Briefly, the fluorescent photons from both bone lead and calcium were counted simultaneously to provide the measurement of lead concentration per unit of bone mineral (microgram microgram /mi·cro·gram/ (µg) (mi´kro-gram) one millionth (10-6) of a gram.
Abbr. per gram). Although the KXRF instrument may generate negative point estimates of bone lead when the true values are close to zero, we have found that retention of all point estimates make better use of the data in epidemiologic studies (21). In addition, only three and one study subjects were found to have the negative values for tibia and patella lead levels, respectively. The technicians who measured the bone lead were blind to the participant's health status.
ALAD exon 4 genotype analysis. The ALAD polymorphism in exon 4 was determined by polymerase chain reaction polymerase chain reaction (pŏl`ĭmərās') (PCR), laboratory process in which a particular DNA segment from a mixture of DNA chains is rapidly replicated, producing a large, readily analyzed sample of a piece of DNA; the process is (PCR PCR polymerase chain reaction.
polymerase chain reaction
Polymerase chain reaction (PCR) ) with restriction fragment length polymorphism restriction fragment length polymorphism
n. Abbr. RFLP
Intraspecies variations in the length of DNA fragments generated by the action of restriction enzymes and caused by mutations that alter the sites at which these enzymes act, changing , according to the methods described by Schwartz et al. (22). We performed PCR reactions in duplicate, with blank controls included in each set.
Statistical analyses. We first compared the distribution of demographic and lifestyle characteristics, bone and blood lead levels, and uric acid and renal function (serum creatinine and estimated creatinine clearance) by genotype (ALAD 1-2/2-2 vs. ALAD 1-1) using chi-squared and Student's t-test statistics. Because only 7 (1%) subjects in this population were ALAD 2-2, our ability to distinguish between effects associated with the ALAD 1-2 versus the ALAD 2-2 genotypes was limited. Nevertheless, initial analyses were conducted comparing wild-type (ALAD 1-1) with ALAD 2-2 individuals alone to see if the homozygous condition was associated with effects that were obscured by combining the ALAD 2-2 and ALAD 1-2 individuals. No such effects were seen; thus, all later analyses were conducted and reported combining ALAD 1-2 and ALAD 2-2 into one category (ALAD 1-2/2-2). Multivariate linear regression was used to model determinants of uric acid and renal function that started with core models including determinants we had identified in previously published studies (15,19). For uric acid (milligrams per deciliter deciliter /dec·i·li·ter/ (dL) (des´i-le?ter) one tenth (10minus;1) of a liter; 100 milliliters.
100 cubic centimeters (cc).
Mentioned in: Hypercholesterolemia ), these core-model determinants included age (years), body mass index [weight (kilograms)/height (meters) (2)], log-transformed alcohol consumption (grams per day), diastolic blood pressure (milligrams mercury), and serum creatinine (milligrams per deciliter); for serum creatinine and estimated creatinine clearance, these core-model determinants included age, body mass index, log-transformed alcohol consumption, hypertension (yes/no), current smoking (yes/no), former smoking (yes/no), and use of analgesic medications (yes/no). Then, blood lead, tibia lead, or patella lead levels were separately forced into the models.
To assess whether genotype may serve as an effect modifier (vs. an independent determinant) of the relationships of blood or bone lead to uric acid and renal function, each of these regressions was then repeated after adding an interaction term for blood or bone lead and genotype (ALAD 1-2/2-2 vs. ALAD 1-1). In addition, we also compared the coefficients of core-model and lead biomarker determinants in regressions of uric acid and renal function that were stratified by genotype (ALAD 1-2/2-2 vs. ALAD 1-1). In each of the above regressions, generalized additive models (23) were to examine the shape of associations between continuous variables (e.g., blood or bone lead) and uric acid and renal function. These analyses allowed us to assess for potential nonlinearities and the need for transforming these covariates. Finally, we applied statistical tests to determine whether a threshold exists between blood or bone lead levels and uric acid or renal function. Akaike's Information Criterion was computed to determine the break point (24). Failure to identify a threshold (break point), if one exists, would erroneously attribute a relationship at low blood or bone lead levels where it is not present (25,26). In addition, such failure would underestimate both the size and significance of the effect at blood or bone levels where it is truly present, by averaging levels where the relationship is nonexistent non·ex·is·tence
1. The condition of not existing.
2. Something that does not exist.
non with those where it is significant. All data were analyzed using the SAS (1) (SAS Institute Inc., Cary, NC, www.sas.com) A software company that specializes in data warehousing and decision support software based on the SAS System. Founded in 1976, SAS is one of the world's largest privately held software companies. See SAS System. (SAS Institute, Cary, NC, USA) and S-PLUS (Insightful Corp, Seattle, WA, USA) statistical packages. All p-values reported are two sided.
Between 1991 and 1995, there were 1,194 active NAS subjects, of whom 776 participated in the KXRF bone lead study. Of these, 710 subjects had all information on serum uric acid and creatinine levels, genotype status, and blood and bone lead levels. One subject with a serum creatinine of 9.0 mg/dL (severe renal disease Renal disease
Mentioned in: Glycogen Storage Diseases
hypertension High blood pressure Cardiovascular disease An abnormal ↑ systemic arterial pressure, corresponding to a systolic BP of > 160 mm Hg ) was excluded (19). No significant differences were found with respect to the distributions of age, body mass index, alcohol consumption, diastolic blood pressure, current smoking status, and blood and bone lead levels among subjects with and without all information (n = 709 vs. 66) on serum uric acid and creatinine, genotype status, and blood and bone lead (data not shown). Therefore, the subsequent analyses were focused on the 709 study subjects.
The prevalence (number) of ALAD 1-1, ALAD 1-2, and ALAD 2-2 was 83.9% (595), 15.1% (107), and 1.0% (7), respectively. Table 1 shows the demographic characteristics, blood and bone lead levels, and serum uric acid and creatinine and estimated creatinine clearance categorized by genotype. Except for age, alcohol consumption, current smoking status, diastolic blood pressure, and blood lead levels, there were no meaningful differences of characteristics by genotype. Subjects with ALAD 1-2/2-2 genotype had a slightly older mean age (68.1 years) and a slightly higher diastolic blood pressure (83.2 mm Hg) than those of the ALAD 1-1 genotype subjects (66.8 years and 80.8 mm Hg). Conversely, the ALAD 1-1 genotype was associated with a higher percentage of current smokers than the ALAD 1-2/2-2 genotype. Blood lead levels in this population were relatively low, as expected, with a mean [+ or -] SD of 6.2 [+ or -] 4.1 [micro]g/dL. We found that mean blood lead level in ALAD 1-1 subjects was slightly and significantly higher than that in ALAD 1-2/2-2 individuals (p = 0.044). The same results were not noted with respect to mean bone lead levels by genotype. The mean [+ or -] SD serum uric acid and creatinine were 6.5 [+ or -] 1.3 and 1.2 [+ or -] 0.2 mg/dL, respectively, for all subjects. We did not find any meaningful difference in mean serum uric acid, serum creatinine, or estimated creatinine clearance between the allele groups.
Our hypotheses were that a) blood lead or bone lead level was a risk factor for hyperuricemia and renal dysfunction and b) ALAD variant type modified this effect especially when blood lead or bone lead level was relatively high (12,27). Table 2 shows the relationship of serum uric acid with bone lead level (patella or tibia lead) with and without an additional term for the interaction of bone lead with genotype, and before (n = 709) and after (n = 638, because of missing data in body mass index, alcohol consumption, and diastolic blood pressure) adjusting for other potential confounders identified in our previous investigation (15). Bone lead level marginally predicted uric acid level after adjusting for age, body mass index, alcohol consumption, diastolic blood pressure, and serum creatinine level (for patella lead, p = 0.078; for tibia lead, p = 0.190; Table 2). When the interaction of patella lead and genotype was added to the regression model, the predictive slope coefficients of serum uric acid by patella or tibia lead level in ALAD 1-2/2-2 individuals was about 50-100% higher than that of ALAD 1-1 subjects ([beta] = 0.006 vs. 0.004 for patella lead and [beta] = 0.009 vs. 0.004 for tibia lead), but the significance levels of the terms were marginal. When we reset the negative values of tibia and patella lead (of which there were only four) to zero, the results were almost identical. We did not find any significant relation of blood lead or its interaction with genotype to serum uric acid (data not shown).
Table 3 shows the relationship of serum creatinine or estimated creatinine clearance with bone lead level with and without an interaction term for bone lead and genotype and before (n = 709) and after (n = 670, because of 39 missing data in body mass index and alcohol consumption) adjusting for other potential confounders identified in our previous investigation (19). Although bone lead level significantly predicted serum creatinine in the crude analysis, we found no significant independent effect of either blood lead or bone lead (tibia lead or patella lead) to serum creatinine after adjusting for age, body mass index, alcohol consumption, hypertension, current smoking status, and current analgesic medications. However, we found a significant interaction of tibia lead (but not blood lead or patella lead) and genotype in relation to serum creatinine (p = 0.025), even though tibia lead level was not a significant independent predictor (Table 3). For estimated creatinine clearance, patella lead was a significant predictor (p = 0.024) after adjusting for age, body mass index, alcohol consumption, hypertension, current smoking status, and current analgesic medications. Neither tibia lead nor blood lead significantly predicted estimated creatinine clearance after adjusting for other covariates. In addition, no interaction was found of blood lead or bone lead with genotype in relation to estimated creatinine clearance (Table 3).
In a smoothed plot of serum uric acid in relation to bone lead that is stratified by genotype and adjusted for other covariates in the model (Figure 1), there is a suggestion of a threshold effect, especially with respect to patella lead, with break points among ALAD 1-1 and 1-2/2-2 genotype individuals at patella lead levels of 101 [micro]g/g and 15 [micro]g/g, respectively, based on the Akaike's Information Criterion (24). Using "hockey stick" regression analyses (25,26), we found a significant linear relationship of serum uric acid with patella lead (p = 0.040; Table 4) above the apparent patella lead threshold level of 15 [micro]g/g among the ALAD 1-2/2-2 genotype individuals, but not among the ALAD 1-1 genotype individuals above the apparent patella lead level of 101 [micro]g/g (p = 0.141).
[FIGURE 1 OMITTED]
We have previously demonstrated that the patella lead level is independently associated with serum uric acid (15). In the present study, our sample was slightly different and the independent effect of patellar lead on serum uric acid was only of marginal significance (p = 0.078); however, we found a significant linear relationship of serum uric acid with patella lead among ALAD 1-2/2-2 genotype individuals who had patella lead levels greater than an apparent threshold of 15 [micro]g/g. There was also a suggestion of a linear relationship of serum uric acid with patella lead among ALAD 1-1 genotype individuals, but with a much higher apparent threshold (~101 [micro]g/g); moreover, the regression coefficient Regression coefficient
Term yielded by regression analysis that indicates the sensitivity of the dependent variable to a particular independent variable. See: Parameter.
regression coefficient for patella was not significant.
This difference between the ALAD 1-2/2-2 and ALAD 1-1 individuals is fairly striking, and suggests that ALAD status modifies the relationship between lead and hyperuricemia with ALAD 1-2/2-2 individuals having a higher risk for lead-induced hyperuricemia. On the other hand, there were relatively few subjects with patella lead levels > 101 [micro]g/g in this community-exposed population (Figure 1). Similar results were found with respect to tibia and blood lead, but they were not as impressive as those for patella lead. The ALAD-2 variant individuals had about a 0.5-2-fold higher serum uric acid than did those with the wild-type ALAD 1-1 (Table 2).
Hyperuricemia is the strongest risk factor for gout. Campion campion: see pink.
Any of the ornamental rock-garden or border plants that make up the genus Silene, of the pink family, consisting of about 500 species of herbaceous plants found throughout the world. et al. (16) found an increased incidence of gout with serum uric acid levels > 9.0 mg/dL. Among patients with lead nephropathy nephropathy /ne·phrop·a·thy/ (ne-frop´ah-the) disease of the kidneys.nephropath´ic
analgesic nephropathy , there is no evidence of overproduction o·ver·pro·duce
tr.v. o·ver·pro·duced, o·ver·pro·duc·ing, o·ver·pro·duc·es
To produce in excess of need or demand.
o of uric acid (28,29). Therefore, chronic lead toxicity causes hyperuricemia mainly due to a defect in the tubular secretion of uric acid. In this study, we found an association between hyperuricemia and bone lead, especially patella lead. Toxic levels of lead (e.g., blood lead levels > 60 [micro]g/dL) are clearly associated with gouty arthritis gouty arthritis Rheumatology A chronic arthropathy characterized by uric acid crystal deposits in the joint which, over time, result in joint erosion. See Acute gouty arthritis, Gout. (15,28). However, to what extent low-level lead exposure contributes to the development of hyperuricemia and clinical risk of gout is unclear. The middle-aged and elderly men in this cohort currently have low levels of lead in blood (mean, 6.2 [micro]g/dL), which may help to explain why our results are not stronger.
Studies in humans have indicated that renal function may be impaired by high levels of lead exposure or prolonged low-level lead exposure (2,19). Renal biopsies in humans with long-term high lead exposure have revealed abnormal renal peritubular and interstitial fibrous tissue fibrous tissue
Tissue composed of bundles of collagenous white fibers between which are rows of connective tissue cells. . Lead-induced interstitial nephritis interstitial nephritis
Nephritis in which the interstitial connective tissue is chiefly affected.
Interstitial nephritis could lead to a true reduction in the glomerular filtration rate glomerular filtration rate
n. Abbr. GFR
The volume of water filtered out of the plasma through glomerular capillary walls into Bowman's capsules per unit of time. or could alter factors that influence the glomerular filtration rate (e.g., surface area, permeability, and oncotic and hydrostatic pressure gradients across the capillary walls) (30). In this cross-sectional study, bone lead level (tibia or patella lead) was positively associated with serum creatinine, but these results did not reach significance after adjusting for other covariates. On the other hand, we detected a positive and significant interaction of tibia lead (but not patella lead) with ALAD genotype in relation to serum creatinine (Table 3), showing ALAD-2 subjects had about 3-4-fold higher serum creatinine than did individuals with ALAD-1. This finding suggests that ALAD may modify the chronic renal toxicity of lead. In a similar vein, Bergdahl et al. (11) did not find any modifying effect of ALAD genotype on the relationship of lead to clinical kidney disease Kidney Disease Definition
Kidney disease is a general term for any damage that reduces the functioning of the kidney. Kidney disease is also called renal disease. indicators among 89 lead-exposed workers, but they did find that the concentrations of urinary calcium and the ratio of urinary creatinine/serum creatinine were significantly lower in the seven ALAD 1-2/2-2 subjects compared with those of the 82 ALAD 1-1 lead workers [median urinary calcium (mg/L), 76 vs. 188; urinary creatinine/ serum creatinine ratio, 84 vs. 180]. Thus, their study did suggest the presence of ALAD allele-specific differences in kidney function. In another study, Smith et al. (10) investigated the association between the presence of ALAD-2 allele, renal function, and lead concentrations in blood and bone among 688 members of a construction trade union. They found marginally higher levels of blood urea nitrogen blood urea nitrogen
n. Abbr. BUN
Nitrogen in the form of urea in the blood or serum, used as a indicator of kidney function.
Blood urea nitrogen (BUN) (p = 0.06) and uric acid (p = 0.09) among the ALAD-2 genotype individuals after adjusting for blood lead level, age, and alcohol consumption. Smith et al. (10) suggested that ALAD-2 genotype may influence chronic renal toxicity by differential binding of lead to the variant ALAD-2 protein. Our results are consistent with these previous reports in demonstrating that ALAD genotype status may modify the relationship between lead and kidney function.
In addition to our findings with serum creatinine, we observed that creatinine clearance, estimated by age, body weight, and serum creatinine, is significantly and negatively associated with bone lead, especially patella lead. One possible explanation is that serum creatinine is not as sensitive a marker for subclinical subclinical /sub·clin·i·cal/ (sub-klin´i-k'l) without clinical manifestations.
Not manifesting characteristic clinical symptoms. Used of a disease or condition. renal damage as is estimated creatinine clearance. Notably, Nolan and Shaikh (30) found that N-acetyl-D-glucosaminidase, a lysosomal lysosomal
pertaining to or emanating from lysosomes.
enzymes located in the lysosomes.
lysosomal phospholipidosis marker of tubular cell toxicity, is a sensitive marker for detecting subclinical kidney damage kidney damage Kidney injury Nephrology A structural or functional compromise in renal function due to external–eg, athletic, occupational, or other trauma, resulting in bruising or hemorrhage, which can be profuse and life threatening Etiology Vascular and is associated with blood lead levels.
We did not find any significant association between blood lead and impaired renal function as measured by serum creatinine or estimated creatinine clearance. Current blood lead level does not represent long-term lead exposure, which may explain why it is not an adequate dosimeter do·sim·e·ter
An instrument that measures the amount of radiation absorbed in a given period.
an instrument used to detect and measure exposure to radiation. with respect to kidney toxicity. Regarding our measures of bone lead, it is not clear why we found that patella bone lead was the best predictor of elevated serum uric acid whereas tibia bone lead was the best predictor of elevated serum creatinine. Compared with the patella, which is composed mostly of trabecular bone trabecular bone
See spongy bone. , the tibia is mostly cortical bone cortical bone
See cortical substance. with a slow rate of bone turnover and a longer half-life with respect to lead levels. As a consequence, the tibia is a better reflection of long-term cumulative lead exposure, whereas the high resorption resorption /re·sorp·tion/ (re-sorp´shun)
1. the lysis and assimilation of a substance, as of bone.
n. rates of trabecular bone make it the most important skeletal source of circulating lead (31). It is possible that lead-induced rises in serum uric acid are mostly dependent on active resorption of bone lead stores, whereas lead-induced rises in serum creatinine are mostly dependent on a cumulative effect of lead on the kidney taking place over many years.
How might this ALAD polymorphism modify the impact of lead on uric acid? The effect of lead on uric acid metabolism has been thought to be mediated by a toxic effect on the proximal renal tubule renal tubule
A tubule of the kidney, such as a collecting or convoluted tubule. , which is the site of uric acid excretion as well as active secretion by renal tubular cells. It is possible that the lead-ALAD-2 subunit complex is more toxic to proximal tubular cells than is the lead-ALAD-1 subunit (11). This same mechanism might be more broadly explanatory of a modifying effect of the ALAD polymorphism on general kidney function, as reflected by our findings with respect to serum creatinine.
Although in in vitro studies and epidemiologic studies suggest that the ALAD-2 polypeptide binds lead more tightly and effectively than does ALAD-1 (3,7,8), the theoretical differential binding of lead by the ALAD isoenzymes does not indicate greater susceptibility to lead for persons with the ALAD-2 genotype. Susceptibility is dependent on different partitioning of lead and how bioavailable different complexed forms of lead are in different tissues. In the present study, ALAD-2 modified lead's relation to uricemia and indices of renal function. However, the modifying influence of ALAD polymorphism on the neurologic effect of lead may be different (12,32). An elevated concentration of plasma [delta]-aminolevulinic acid, an early biologic effect of lead poisoning lead poisoning or plumbism (plŭm`bĭz'əm), intoxication of the system by organic compounds containing lead. , was higher in 44 battery workers with homozygous ALAD-1, compared with 21 ALAD-2 workers (12). Sithisarankul et al. (12) suggested that if the neurologic effects of lead poisoning are partly due to elevated [delta]-aminolevulinic acid, then the ALAD-2 genotype may be protective for this end point. This is consistent with the results of a study of neuropsychologic effects of lead in adolescents, showing that the ALAD-2 subjects performed better on tests of attention than did the ALAD-1 subjects after adjusting for lead exposure (32). These potential contrasting roles of ALAD genotype demand further study to clarify the effect of susceptibility to lead toxicity.
Our study has a number of limitations including its cross-sectional epidemiologic design and, perhaps most important, its focus on community-exposed men with relatively modest lead burdens, as reflected by bone lead levels less than a third of those seen in workers in a primary lead industry, such as lead smelting (11,33). It is quite possible that the modifying effect of ALAD polymorphism on lead toxicity would be more apparent among populations with higher levels of lead exposure. Clearly, our findings must be viewed only as suggestive, and other studies are needed to see if these relationships can be replicated.
In conclusion, we found evidence that a polymorphism of ALAD that has been the recent focus of research may modify the impact of lead on uric acid excretion and general kidney function, with ALAD-2 carriers manifesting effects at levels of lead burden with an apparently lower threshold than that of ALAD 1-1 individuals. Additional research is required to determine if this represents a true gene-environment interaction with clinical significance.
Table 1. Demographic characteristics and blood and bone lead concentrations by genotypes among 709 study subjects, 1991-1995. Genotype [mean [+ or -] SD (range)] Total ALAD 1-1 Variable (n = 709) (n = 595) Age (years) 67.0 [+ or -] 7.4 66.8 [+ or -] 7.3 (48.0-93.0) (48.0-93.0) Body mass index 27.8 [+ or -] 3.9 27.7 [+ or -] 3.8 (kg/[m.sup.2]) (b) (16.7-44.9) (16.7-44.9) Diastolic blood pressure 81.2 [+ or -] 9.8 80.8 [+ or -] 9.7 (mmHg) (c) (51.0-119.0) (51.0-119.0) Alcohol consumption 12.9 [+ or -] 17.5 13.5 [+ or -] 17.9 (g/day) (c) (0-103.9) (0-103.9) Blood lead ([micro]g/dl) 6.2 [+ or -] 4.1 6.3 [+ or -] 4.1 (0-35) (0-35) Bone lead ([micro]g/g) Tibia 22.0 [+ or -] 13.4 22.1 [+ or -] 13.9 (-3-126) (-3-126) Patella 32.1 [+ or -] 19.5 32.2 [+ or -] 20.0 (-10-165) (1-165) Uric acid (mg/dL) 6.5 [+ or -] 1.3 6.4 [+ or -] 1.3 (2.9-10.6) (2.9-10.6) Serum creatinine (mg/dL) 1.2 [+ or -] 0.2 1.2 [+ or -] 0.2 (0.6-2.5) (0.6-2.5) Estimatec creatinine 71.3 [+ or -] 21.2 71.6 [+ or -] 20.8 clearance (mL/min) (b) (16.9-215.7) (24.1-215.7) Hypertension [n(%)] Yes 528 (74.5) 445 (74.8) No 181 (25.5) 150 (25.2) Current smoking status [n(%)] Never smoker 215 (30.3) 174 (29.2) Former smoker 432 (60.9) 362 (60.8) Current smoker 62 (8.7) 59 (9.9) Current analgesic medications Yes 538 (75.9) 450 (75.6) No 171 (24.1) 145 (24.4) Genotype [mean [+ or -] SD (range)] ALAD 1-2/2-2 Variable (n = 114) p-Value (a) Age (years) 68.1 [+ or -] 7.5 0.075 (52.0-93.0) Body mass index 28.3 [+ or -] 4.3 0.214 (kg/[m.sup.2]) (b) (18.8-41.5) Diastolic blood pressure 83.2 [+ or -] 9.9 0.021 (mmHg) (c) (64.0-106.0) Alcohol consumption 9.3 [+ or -] 14.7 0.011 (g/day) (c) (0-77.9) Blood lead ([micro]g/dl) 5.8 [+ or -] 4.2 0.044 (d) (0-27) Bone lead ([micro]g/g) Tibia 21.5 [+ or -] 11.0 0.816 (e) (3-67) Patella 31.1 [+ or -] 17.0 0.612 (e) (-10-85) Uric acid (mg/dL) 6.6 [+ or -] 1.3 0.211 (3.6-9.7) Serum creatinine (mg/dL) 1.3 [+ or -] 0.3 0.222 (0.6-2.4) Estimatec creatinine 70.0 [+ or -] 23.3 0.472 clearance (mL/min) (b) (16.9-130.4) Hypertension [n(%)] Yes 83 (72.8) 0.656 (f) No 31 (27.2) Current smoking status [n(%)] Never smoker 41 (36.0) 0.016 (g) Former smoker 70 (61.4) Current smoker 3 (2.6) Current analgesic medications Yes 88 (77.2) 0.721 (f) No 26 (22.8) (a) Determined by Student's t-test except where noted. (b) Three missing in ALAD 1-1 and one missing in ALAD 1-2/2-2. (c) Twenty-seven missing in ALAD 1-1 and nine missing in ALAD 1-2/2-2. (d) Determined by Student's t-test after taking the natural logarithm of blood lead. (e) Determined by Student's t-test after adding the value of 35 and then taking the natural logarithm of all values. (f) Chi-square test. (g) Fisher's exact test. Table 2. Relationship of uric acid (mg/dL) with bone lead ([micro]g/g) in multivariate linear regression without and with ALAD genotype interaction in the Normative Aging Study, 1991-1995. Crude analyses (n = 709) Regression Regression Variable coefficient p-Value coefficient (b) p-Value Patella Lead 0.005 0.048 0.004 0.093 Lead-ALAD (c) -- -- 0.007 0.074 Tibia Lead 0.006 0.089 0.005 0.169 Lead-ALADC -- -- 0.012 0.028 Adjusted analyses (n = 638) (a) Regression Regression Variable coefficient p-Value coefficient (b) p-Value Patella Lead 0.005 0.078 0.004 0.129 Lead-ALAD (c) -- -- 0.006 0.089 Tibia Lead 0.005 0.190 0.004 0.274 Lead-ALADC -- -- 0.009 0.080 (a) Adjusted for age (years), body mass index, log-transformed alcohol consumption (g/day), diastolic blood pressure (mm Hg), and serum creatinine (mg/dL); some variables have missing data. (b) Lead-ALAD interaction in the regression model. (c) Interaction between bone lead and genotype (ALAD 1-2,/2-2 vs. ALAD 1-1). Table 3. Relationship of serum creatinine or estimated creatinine clearance with bone lead ([micro]g/g) without and with ALAD genotype interaction in the Normative Aging Study, 1991-1995. Crude analyses (n = 709) Regression Regression coefficient Variable coefficient p-Value (b) p-Value Serum creatinine (mg/dL) Patella Lead 0.001 0.021 0.0008 0.053 Lead-ALAD (c) -- -- 0.002 0.024 Tibia Lead 0.002 0.019 0.001 0.055 Lead-ALAD (c) -- -- 0.003 0.003 Estimated creatinine clearance (mL/min) Patella Lead -0.190 < 0.001 -0.186 < 0.001 Patella Lead-ALAD (c) -- -- -0.042 0.485 Tibia Lead -0.271 < 0.001 -0.263 < 0.001 Lead-ALAD (c) -- -- -0.090 0.310 Adjusted analyses (n = 670) (a) Regression Regression coefficient Variable coefficient p-Value (b) p-Value Serum creatinine (mg/dL) Patella Lead 0.0004 0.408 0.0003 0.518 Lead-ALAD (c) -- -- 0.0009 0.172 Tibia Lead 0.0006 0.354 0.0005 0.495 Lead-ALAD (c) -- -- 0.002 0.025 Estimated creatinine clearance (mL/min) Patella Lead -0.069 0.024 -0.0690 0.026 Patella Lead-ALAD (c) -- -- -0.006 0.884 Tibia Lead -0.078 0.082 -0.0750 0.098 Lead-ALAD (c) -- -- -0.044 0.499 (a) Adjusted for age (years), body mass index, hypertension (yes/no), current smoking (yes/no), former smoking (yes/no), log-transformed alcohol intake (g/day), and current analgesic medications (yes/no); some variables have missing data. (b) Lead-ALAD interaction in the regression model. (c) Interaction between genotype (ALAD 1-2/2-2 vs. ALAD 1-1). Table 4. Relationship of uric acid (mg/dL) with patella lead ([micro]g/g) by genotype in the Normative Aging Study, 1991-1995. (a) ALAD 1-1(n =540) Parameter Variable (b) estimate t-Statistic p-Value Patella lead > 101 [micro]g/g 0.021 1.473 0.141 Patella lead > 15 [micro]g/g -- -- ALAD 1-2/2-2(n = 98) Parameter Variable (b) estimate t-Statistic p-Value Patella lead > 101 [micro]g/g -- -- -- Patella lead > 15 [micro]g/g 0.016 2.084 0.040 (a) Some variables with missing data. (b) Adjusted for age (years), body mass index, log-transformed alcohol consumption (g/day), diastolic blood pressure (mm Hg), and serum creatinine (mg/dL).
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Address correspondence to H. Hu, Channing Laboratory, Harvard Medical School Harvard Medical School (HMS) is one of the graduate schools of Harvard University. It is a prestigious American medical school located in the Longwood Medical Area of the Mission Hill neighborhood of Boston, Massachusetts. , 181 Longwood Avenue, Boston, MA 02115 USA. Telephone: 617 432 2790. Fax: 617 525 0362. E-mail: howard.hu@ channing.harvard.edu
We gratefully acknowledge the research assistance of S. Harcourt, R. Heldman, G. Barbella, S. Oliveira, T. Luu, G. Fleischaker, M. Barr, L. Hennessey, and S. Datta. We thank D. Burger and F. Milder for technical assistance in the initial phase of our KXRF measurements and J. McCoy for editorial assistance. We are indebted to the continued enthusiastic cooperation of the participants in the Normative Aging Study.
Support for this research was provided by National Institute of Environmental Health Sciences The National Institute of Environmental Health Sciences (NIEHS) is one of 27 Institutes and Centers of the National Institutes of Health (NIH),which is a component of the Department of Health and Human Services (DHHS). The Director of the NIEHS is Dr. David A. Schwartz. (NIEHS NIEHS National Institute of Environmental Health Sciences (NIH, DHHS) ) grants ES 05257-06A1 and P42-ES05947 (with funding from the U.S. Environmental Protection Agency Environmental Protection Agency (EPA), independent agency of the U.S. government, with headquarters in Washington, D.C. It was established in 1970 to reduce and control air and water pollution, noise pollution, and radiation and to ensure the safe handling and ) and NIEHS Occupational and Environmental Health Center grant 2 P30 ES00002. M.-T.W. received an award from the American Bureau for Medical Advancement in China, Inc. The Normative Aging Study is supported by the cooperative studies program/ERIC, Department of Veterans Affairs, and is a component of the Massachusetts Veterans Epidemiology Research and Information Center. Subjects were evaluated in the outpatient Clinical Research Center of the Brigham and Women's Hospital with support from National Institutes of Health (NIH "Not invented here." See digispeak.
NIH - The United States National Institutes of Health. ) grant NCRR NCRR National Center for Research Resources
NCRR North Carolina Railroad
NCRR Nikkei for Civil Rights & Redress
NCRR Network Cost Reduction Ratio
NCRR Non Conformance Release Report GCRC GCRC General Clinical Research Center
GCRC Great Canadian Railtour Company
GCRC Graafschap Christian Reformed Church (Holland, Michigan)
GCRC Galena Creek Rock Glacier M01RR02635. The KXRF instrument used in this work was developed by ABIOMED, Inc., Danvers, MA, USA, with support from NIH grant SBIR SBIR Small Business Innovation Research (program/grant)
SBIR Space Based Infra-Red
SBIR Speaker-Boundary Interference
SBIR Site Backsurface-referenced Ideal Plane/Range (silicon wafers) 2R44 ES03918-02.
Received 25 January 2002; accepted 2 August 2002.
Ming-Tsang Wu, (1,2,3) Karl Kelsey, (1,4) Joel Schwartz, (1) David Sparrow, (5) Scott Weiss, (4) and Howard Hu (1,4)
(1) Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts, USA; (2) Graduate Institute of Occupational Safety and Health and (3) Department of Occupational Medicine, Kaohsiung Medical University The Kaohsiung Medical University (Traditional Chinese:高雄醫學大學), originally known as "Kaohsiung Medical College", is a private university located in Kaohsiung, Taiwan. Hospital, Kaohsiung, Taiwan; (4) Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA; (5) The Normative Aging Study, U.S. Department of Veterans Affairs, Boston, Massachusetts, USA