- Open Access
Elevated blood lead levels among unskilled construction workers in Jimma, Ethiopia
© Gebrie et al.; licensee BioMed Central Ltd. 2014
- Received: 20 September 2012
- Accepted: 10 March 2014
- Published: 19 March 2014
No study has been carried out to assess the blood lead levels of workers or the contribution of common workplace practices to lead exposure in Ethiopia. This study was carried out to assess the blood lead levels of female and male laborers in the construction sector in Jimma town, Ethiopia.
A cross-sectional study on the blood lead levels of 45 construction workers was carried out in the town of Jimma. The t-test, analysis of variance, the Kruskal-Wallis, Mann–Whitney and odds ratio tests were used to compare mean blood lead levels and to investigate the associations between specific job type, use of self-protection device, sex, service years and occurrence of non-specific symptoms with BLLs.
The mean blood lead level of the exposed group (40.03 ± 10.41 μg/dL) was found to be significantly greater than that of the unexposed group (29.81 ± 10.21 μg/dL), p = 0.05. Among the exposed group female workers were found to have higher mean blood lead level (42.04 ± 4.11 μg/dL) than their male colleagues (33.99 ± 3.28 μg/dL). Laborers who were regularly using self-protection devices were found to have significantly lower blood lead levels than those who were not using.
The blood lead levels of construction workers in Jimma town are considerably high with a range of 20.46 – 70.46 μg/dL and the workers are in danger of imminent lead toxicity. More endangered are female construction workers who are bearers of the future children of the country and the issue requires urgent attention.
- Blood lead level
- Construction workers
- Non-specific symptoms
- Self-protection device
Lead is a cumulative and persistent toxic substance that poses a serious health risk to humans. In the general population, lead exposure arises from food, drinking water, occupation, hobbies or, to a lesser degree, atmospheric lead contamination . Several investigators have also observed that lifestyles such as smoking cigarettes and alcohol contribute to lead uptake in humans [2–6]. Lead intoxication is dangerous to all people in all sectors but children are more vulnerable due to their lifestyle, rapid growth and still developing systems. Urban children in developing countries are known to be most at risk of lead intoxication and it was estimated in 1994 that over 80% of those between three and five years of age and 100% under two had average blood lead levels (BLLs) exceeding the threshold of 10 mg/dL set by the United States Centre for Disease Control (US-CDC) [3, 5]. Children intoxicated with lead are more likely to have birth defects, mental retardation, or behavioural disorders or to die during the first year of childhood .
Once in the body, lead circulates in the blood; while most is excreted, some can remain in the tissues, organs and bones. From the skeleton as a primary storage site, lead gradually reenters the circulation through bone resorption . In pregnant women, lead sequestered in the bone from past exposure or that accumulated in the body from recent exposure can be carried to the unborn baby by mobilization via the placenta. As a result, exposure to lead for women of childbearing age can have adverse effects on their offspring, should they become pregnant .
Exposure to lead is characterized by subtle, non-specific symptoms that frequently contribute to misdiagnosis of lead poisoning and the onset of symptoms depend on whether the intoxication was acute or chronic. Signs of chronic lead poisoning include weakness, excessive tiredness, irritability, constipation, anorexia, abdominal discomfort (colic), fine tremors and ‘wrist drop’. Overexposure to lead may also result in damage to the kidneys, anaemia, high blood pressure, impotence, infertility, and reduced sex drive in both sexes . Although the WHO and CDC defined BLLs of 25 μg/dL as toxic in 1991, the scientific consensus is that there is no exposure level below which lead appears to be safe and action is being taken to reduce the international accepted levels of action [10, 11]. Estimates published recently suggest that the theoretical minimum risk may occur at blood lead concentrations as low as 0 – 1 μg/dL . Believing that some of the effects of lead, particularly changes in the levels of certain blood enzymes and in aspects of children’s neurobehavioral development, may occur at blood levels so low as to be essentially without a threshold, the US Environmental Protection Agency (EPA) and US Agency for Toxic Substances and Disease Registry (ATSDR), declined to specify a level of exposure not likely to lead to adverse effects for lead . For lead, therefore, any exposure is of potential concern.
Lead poisoning has been identified as an occupational hazard from ancient times. A wide variety of industrial populations such as: people who work in lead smelting and refining industries and those who deal with lead during the manufacturing process, construction workers and people who work in pottery and ceramic industries could all be exposed to high lead levels . In Ethiopia the construction sector is currently employing a huge number of unskilled general labourers, both men and women. Due to the better pay that the construction sector offers, many women who were working as maids in private homes and those who were jobless are joining the sector. They are employed mostly as unskilled labourers and are involved in jobs such as: demolishing, manual scraping, concreting, plastering, painting, etc. Most of these laborers eat their lunch at the work place sitting at any corner in the site under dusty conditions. They have no access to wash their hands before they eat. As lead is most commonly absorbed into the body by inhalation, the workers can absorb lead dust produced when metal is cut or when lead paint is windblown during demolition of old houses that existed on the construction sites or, from the fumes resulting from manual spray painting of metallic doors . Moreover, lead dust can settle on the hands and clothes of the workers when they handle lead containing activities. They can then ingest the lead that has settled on their hands and/or on their food when they eat, drink or smoke without washing their hands. So, really at issue is that they are not aware of the potential dangers and have not had Workplace Hazardous Materials Information System (WHMIS) training and even if they did, there is little beyond using face masks, which they could do to protect themselves and their families. As a result, the level of lead in construction workers in general can be greater than that of the general population and the level in females may also be greater than the maximum tolerable limit in women of child bearing age.
In Ethiopia, no investigation has been carried out on the occupational lead exposure of workers except the cross-sectional study carried out in Addis Ababa on workers in lead acid battery repair units of transport service enterprises, and the study carried out in Jimma on the BLL of auto-garage workers [15, 2]. In addition to this, there are no statistical data that show the number of workers at risk due to lead exposure. Therefore, the main objective of this research was to determine the BLLs of unskilled male and female labourers working in the construction sector in Jimma town and compare their relative workplace exposure to lead. However, since the BLL of the general population is not monitored in Ethiopia, reference ranges of BLLs that can be used by researchers or physicians to determine whether an individual has been exposed to higher levels than are found in the general population are not established. As a result individuals who were not working in the construction sector were included in this study to find out whether the BLLs and associated non-specific symptoms in the construction workers were significantly different from those of the general population.
Study area and sample selection
Jimma is a small town in South West Ethiopia. There are no major industrial sources of lead emission in the town. There are however, several small scale metal workshops, auto-garages and lead acid battery repair units of transport service enterprises and nearly all are located in the center of the town. The central bus station of the town is also found in the town center and emissions from car fuel exhaust and from other industrial activities are high in this part of the town. Residents of this part of the town are expected to be exposed to ‘high’ amount of atmospheric lead relative to residents living in areas ‘far’ from the center.
The current growth in the construction sector in the town has attracted many jobless young male and female residents of the town or from the surrounding rural areas. Three construction sites with relatively large number of workers (50 – 75) were purposively selected for the current study. About two thirds of the laborers in the selected construction sites were females. With the permission of the respective site managers, the workers were approached and requested to participate in the study on a voluntary basis after the purpose of the study was clearly explained to them. Finally, 35 female and 10 male workers (occupationally exposed) were found to fulfill the inclusion criteria (a duration of at least 6 months on the job and, residential place ‘far’ , at least 3 kms, from the town center) and all agreed and participated in the study voluntarily. Oral and written consent was obtained from each participant. Thirty female and fifteen male boarding students of Jimma University who had apparently no history of lead exposure, were non-smokers, non-alcoholics and supposed to be unexposed, were selected from among those who stayed in the University for at least 6 months and asked to participate in the study. Five of the female students and four of the male refused to donate blood samples while twenty five females and eleven males expressed their willingness and donated blood samples. This group served as the control group. The dormitories of the selected students were located about 5 kms North-East of the town center. The study was conducted after obtaining ethical approval from the Ethical and Research Committee of the College of Public Health and Medical Sciences at Jimma University.
Reagents and chemicals
Analytical standard solutions of lead (Spectro ECON) were prepared by serially diluting a 1000 mg/L stock calibration standard solution. Reagents used included trichloroacetic acid (5%; TCA) and perchloric acid (extra pure, Riedel-de Haen, Germany), K2EDTA and ammonium pyrollidine dithiocarbamates (APDC; Merck (Darmstadt), calcium chloride and methyl iso-butyl ketone (MIBK; Sigma Chemical Co).
Blood sample collection and analysis
A venous blood sample (about 5 mL) was collected from each study unit by qualified medical laboratory professionals into a labeled heparinized blood collection vacutainer tubes containing 7.2 mg of K2EDTA. Separate sterilized needle and glove was used for each individual. The samples were homogenized by hand shaking and 2 mL from each sample was transferred into separate pyrex test tubes. To this, 4.0 mL of 5% TCA was added to make the Blood:TCA volume ratio 2:1. To this mixture, 1.3 mL of 2 M perchloric acid, 0.8 mL of APDC- surfactant solution, 50 μL 1.5 M CaCl2, and 2.0 mL water saturated MIBK were added successively and shaken for about 20 seconds. The resulting mixtures were centrifuged for 10 minutes at 2000 rpm using PLC-02 Gemmy, Taiwan, centrifuge. The Pb-APDC solution was analyzed in MIBK within 2 hours of extraction. All used needles and gloves were packed in appropriately labelled disposable bags and disposed into the Jimma University Specialized Hospital waste disposal unit.
The concentration of lead in the blood samples was determined by Flame Atomic Absorption Spectrometer (NovAA 300) at 283.3 nm after optimizing the various analytical parameters. Blood from each study unit was measured in triplicate and averages of triplicate measurements were taken for each experimental unit participant’s sample. Instrument drift was controlled by running standards after the successive analysis of 10 samples. Quantification of lead in blood was done with the use of a standard curve (0–2 ppm) prepared from a commercial lead standard. For quality assurance, due to unavailability of Standard Reference Material (SRM) in our laboratory, validation of the analytical protocol was done by the standard addition method of the metal. Percentage recoveries determined from blood samples fortified with 10 μg of lead per 4.0 mL of blood sample averaged 94.6%. However, no correction for recoveries was performed on the data. The limit of detection for lead was determined from the concentration equivalent of three times the standard deviation of 7 determinations at 0.05 ppm lead. Uniformity of variance was tested by carrying out 7 additional determinations at 0.1 ppm lead solution. The limit of detection determined from the pooled standard deviation was found to be 0.054 mg/L.
In addition to blood lead concentration analysis, standardized questionnaires, designed to yield the required information from each participant, consisting of 35 questions for the exposed and 29 for the unexposed were completed during face-to-face interviews privately. Both groups answered the same 29 questions regarding demographic data, socioeconomic status, habits, perceived health, and non-specific symptoms related to elevated BLL. The remaining 6 questions were specific to the exposed group. The questionnaires were prepared in English but translated into the local language for those who did not understand English.
Data analysis was carried out using SPSS version 16.0. Statistical analysis of BLLs and other data obtained through questionnaire was carried out by categorizing the exposed and/or unexposed groups by sex, specific job type, occurrence of non-specific symptoms, alcohol consumption habit and service year. Descriptive statistics was used to cross tabulate factors by study groups. The parametric independent t-test, was used for the comparison of mean BLLs of exposed and unexposed cohorts. Comparisons of skewed categorical data were performed by using the non-parametric Kruskal Wallis and Mann–Whitney U-tests. The Fisher’s Exact Ratio test was used to evaluate the occurrence of non-specific symptoms among the individuals in the exposed group relative to those of unexposed group. The chi-square was used to test the dependence of BLL on service year.
Characteristics of study units
The mean BLLs of the females and males in each of the two cohorts was also calculated and, that of female workers in the exposed group (42.04 ± 4.11 μg/dL, range: 21.64 – 58.76 μg/dL), was found to be higher than that of their male colleagues (33.99 ± 3.28 μg/dL, range: 20.46 – 38.12 μg/dL), female members of the unexposed group (27.28 ± 2.76 μg/dL, range: 12.43 – 46.65 μg/dL), and male members of the unexposed group (35.35 ± 4.48 μg/dL, range: 12.78 – 45.84 μg/dL). According to the Kruskal-Wallis test the BLLs of the four groups were found to be significantly different at p = 0.05. The Mann–Whitney U-test performed between pairs of groups has also shown that the BLL of the female workers in the exposed group was significantly greater than that of each of the other groups (p < 0.05). On the other hand, in the unexposed cohort the mean BLL of males was significantly higher than that of the females (p < 0.05).
Number of the exposed and unexposed individuals with BLLs in different concentration ranges
№ and% of individuals in the exposed group
№ and% of individuals in the unexposed group
BLL range (μg/dL)
n (nM, nF)
% T (% M, % F)
n (nM, nF)
% T (% M, % F)
10 – 20
8 (1, 7)
22 (2.8, 19)
20 – 35
13 (7, 6)
28.89 (15.6, 13)*
15 (4, 11)
41.67 (11, 30.6)
35 – 40
12 (2, 10)
26.7 (4.5, 22)
6 (1, 5)
16.67 (2.8, 13.9)
40 – 45
7 (0, 7)
15.6 (0, 15.6)
5 (4, 1)
13.89 (11, 2.8)
45 – 50
5 (0, 5)
2 (1, 1)
5.56 (2.8, 2.8)
50 – 55
4 (0, 4)
8.9 (0, 8.9)
55 – 60
7 (0, 7)
15.6 (0, 15.6)
1 (1, 0)
2 (2, 0)
Among members of the exposed group, all males had BLLs in the range of 20 and 40 μg/dL and all the higher BLLs were recorded for female members except one, 70.46 μg/dL, that corresponds to male member of the exposed group. In the unexposed group the lower BLL ranges are dominated by females while the higher ranges, specifically 40 – 45 μg/dL, was dominated by males.
BLL and age relationship
Mean BLL and number of the exposed individuals in different age group
Number (%) of workers
Mean BLL (Mean ± SD) μg/dL)
18 – 25
29.3 ± 7.1
39.7 ± 6.7
36.3 ± 7.3
26 – 35
32.2 ± 6.4
46.8 ± 8.5
44.4 ± 9.8
36 – 45
47.7 ± 7.5
44.8 ± 9.2
46 – 49
46.2 ± 3.6
46.2 ± 3.6
BLL and specific job type
The mean, maximum and minimum BLLs of the construction workers involved in different job categories
Labor of division
Mean ± SD
44.55 ± 9.47
Stone carriers/concrete mixers
36.65 ± 8.48
39.76 ± 11.79
Use of SPD and alcohol drinking habit
As can be seen from the bar graph the mean BLL of members of the exposed group who were using SPD while at work and who were not alcohol consumers, was 29.66 ± 6.15 μg/dL (males 25.99 ± 5.95 μg/dL, n = 4, females 31.76 ± 6.51 μg/dL, n = 7). On the other hand, the mean BLL of the members who were not using SPD while at work and were not alcohol consumers was 41.33 ± 9.36 μg/dL (males 40.59 ± 17.13 μg/dL, n = 5; females 42.74 ± 7.07 μg/dL, n = 21); and that of members who were not using SPD and were alcohol consumers was 47.67 ± 8.26 μg/dL (males 36.66 μg/dL (n = 1), females 49.51 ± 7.32 μg/dL, n = 6). According to the Kruskal-Wallis test, the observed difference between the BLLs of the three groups was significant (p < 0.05).
BLL and service year
According to the chi-square test the observed difference was not, however, significant at p = 0.01. On the contrary, the relative number of individuals with BLLs ranging 20 – 30 μg/dL in the 1 – 3 service year group was lower than that of individuals with BLLs between 30 – 40 or greater than 40 μg/dL. Among the workers in the 3 – 10 service year group no worker had a BLL in the 20 – 30 μg/dL range. In the 1 – 3 service year group 39 and 44% of individuals were found to have BLLs between 30 – 40 μg/dL and greater than 40 μg/dL respectively, while among those in the 3 – 10 service year group, those with BLLs between 30 – 40 and greater than 40 μg/dL were 50% each. The chi-square test has revealed that the difference in the number of individuals with BLLs between 20 – 30, 30 – 40 and greater than 40 μg/dL among the workers in 1 – 3 or 3 – 10 service year categories was significant (p = 0.01). The difference in the number of individuals with BLLs between 30 – 40 and greater than 40 μg/dL in both service year groups, however, was not significant (p = 0.01). With an increase in service year, the proportion of individuals with lower BLL was found to decrease while that of individuals with higher BLLs was increasing. This clearly shows the direct relationship between BLL of the construction workers and service year.
Lead toxicity symptoms
Reported symptoms among the exposed (n = 45) and the unexposed (n = 36) groups and the ratios of their odds
№ and% of ‘yes’ response for symptom
0.25 - 25
0.86 - 21
0.12 – 2.7
0.49 – 14
3.8 - 83
1.1 – 73
Lack of appetite
0.25 - 25
0.9 - 64
0.25 - 25
1.0 – 6.2
Since 1980, when the WHO specified a BLL of 40 μg/dL in the general population and 30 μg/dL in women of childbearing age, the so called “safe BLL” in humans has undergone a number of revisions with the advancement of knowledge on the toxicity of lead at lower concentrations. Although no threshold has been determined for the harmful effects of lead, the Centers for Disease Control and Prevention (CDC) considers BLL ≥10 μg/dL to be of health concern for children, and BLLs ≥25 μg/dL for adults . Moreover, a UNEP-UNICEF document advises the beginning of treatment within 48 hours for BLL exceeding 45 μg/dL and a BLL more than 70 μg/dL as presenting a medical emergency . However, a number of recent studies demonstrate that lead inflicts significant damage even at BLLs below 5 μg/dL and recommends that level be kept below 10 μg/dL and, pregnant women or women considering pregnancy should not have a BLL above 5 μg/dL [18–20]. The results of this study have revealed that the BLL of unskilled construction workers ranges between 20.46 μg/dL and 70.46 μg/dL and that of non-construction workers between 12.43 μg/dL and 46.65 μg/dL. The difference between the BLLs of the two groups was significant. The BLL results in this study indicate that, both the general population and the construction workers are exposed to lead but the exposure of the construction workers is significantly higher than that of the general population.
Sixteen (35%) of the construction workers and 2 (5.7%) of the unexposed group had BLLs exceeding 45 μg/dL. According to the suggestion given in the UNEP-UNICEF document, these were people who should have begun treatment within 48 hours . The BLL of one person in the exposed group was at the border of the limit considered to present a medical emergency. Other studies on the occupational exposure of different groups have reported similar ranges of BLLs with that of this study. For example, Fatoki and Ayoade assessed the level of lead in blood samples of occcupationally and non-occupationally exposed donors in Ile-Ife, Nigeria, and they found a BLL range of 28.75 ± 17.3 μg/dL – 35.5 ± 15 μg/dL in the occupationally exposed cohorts . A cross-sectional study conducted to determine the status of environmental and occupational lead exposure in Nairobi, Kenya, reported a wider BLL range for the occupationally exposed group, 5.8 to 65 μg/dL, with a mean value of 22.6 ± 13.4 μg/dL . Although the mean value in the Nairobi study is much lower, the BLL range of the group studied is similar to that of this specific study in Ethiopia. Aliasgharpour and Hagani determined the BLLs of a group of 31 male non-smoking industrial workers and found BLL ranging between 15.50 μg/dL and 59.99 μg/dL . Rabin and co-workers reported that 63% of 381 registrants in the Massachusetts Occupational Lead Registry with BLLs of 40 μg/dL or higher are construction workers . Their finding was slightly greater than that of this study in which the percent of construction workers with BLLs of 40 μg/dL and above were 53.34%. A study conducted in United Arab Emirates (UAE) on 100 industrial workers (exposed) and 100 non-industrial workers (non-exposed) to determine the effect of blood lead on the health of industrial workers reported a mean of BLL of 77.5 ± 42.8 μg/dL in the industrial workers and 19.8 ± 12.3 μg/dL in the non-industrial workers .
Following recommendations of the Council of State and Territorial Epidemiologists (CSTE) in 2009, the CDC/NIOSH Adult Blood Lead Epidemiology and Surveillance (ABLES) program changed their case definition of elevated BLL from greater than 25 μg/dL to greater than10 μg/dL based on evidence linking lower levels of lead in adults with decreased kidney function, cardiovascular disease and cognitive impairment . The BLLs of the unexposed group in this study were all above 10 μg/dL, higher than the current CDC/NIOSH definition of elevated BLL, and 77.78% of them had BLL exceeding 20 μg/dL. A BLL exceeding 20 μg/dL is known to indicate a substantial exposure to lead. The findings of the current study are in accordance with the findings in our previous study , which showed a similar high BLL in the general population. This may be a clear indication of the fact that the general population is also exposed to lead from various other sources in the environment. In general, the community is exposed to lead from food, water, and air that may be present in hazardous concentrations. A similar report in which students and individuals working in an open environment with greater exposure to environmental pollution was given by Yakub and Iqbal .
The results of this study have also shown that, the mean BLL of the construction workers who were using SPD was significantly lower than that of the construction workers who were not using SPD while at work. Among the female construction workers, only 20% were SPD users while 60% of the male construction workers were using SPD while at work. The female construction workers who were not using SPD were also found to have significantly higher BLL than their female colleagues who were using SPD. These findings suggest that the use of SPD can significantly reduce the level of lead exposure by construction workers. Moreover, among the construction workers who were not using SPD, the BLL of those who were alcohol consumers was significantly higher than that of their colleagues who were not consuming alcohol. This might indicate the possible enhancement of lead accumulation in the blood by alcohol. Similar findings were reported by other researchers [2–6].
In Ethiopia only men were involved in construction related jobs some 10 to 15 years ago. Most uneducated jobless women were employed in private homes as maids. Currently however, due to the better pay that the construction sector offers, many of these women and those who had no job at all, are joining the construction sector and their number is increasing from time to time. All of these women are employed as unskilled labourers and are involved in all job types their male colleagues are involved in: demolishing, manual scraping, concreting, plastering and painting. Among the exposed group, in the current study, the BLL of females was found to be significantly greater than that of males. The findings of this study have also shown that the number of female construction workers who were using SPDs while at work was significantly lower than that of males. Statistical analysis has shown a positive correlation between BLL and not using SPDs.
In most Ethiopian families, due to cultural taboo, the routine house hold activities such as food preparation are undertaken by females only. Males are not expected to get into kitchen and prepare food, clean dish or do some other related activities. The females use clay pans for baking ‘injera’ , leavened bread prepared by fermentation of teff (Eragrostis abyssinica Schrad), wheat, barley, maize or sorghum, or from a mixture of these. They also use clay or metallic bowls for the preparation of ‘wot’ , a spiced sauce prepared from legumes, vegetables or meat depending on the income of the family. Therefore, women can be exposed to any lead originating from the materials they handle while carrying out these activities which are not handled by men. This could be a possible confounder in our study. Therefore, we cannot exclusively conclude that lack of using SPDs in the work place is the only reason for the higher BLLs of the female workers than those of males. Another possible reason for the higher BLL in females, reported in the literature, could be sex difference either in uptake or retention of lead. In a comparison between the relative retention of lead by men and premenopausal women, it has been found that, premenopausal women retain lead more avidly or release lead more slowly than do men and pointed out that this distinction is lost for postmenopausal women . This conclusion fits that of our observation since all the women included in our study were premenopausal, according to the responses they gave during interview.
The mean BLL of the unexposed group was found to be positively correlated with age while that of the exposed group was not. This might be a relation that would discriminate between occupational and non-occupational lead exposure. Gradual exposure to environmental lead by the non-occupationally exposed group may cause gradual increase in BLL with age. In the exposed group, however, exposure to high level of lead in a relatively shorter period at the work place in addition to the exposure from other environmental sources might cause the workers to accumulate high amount of lead in a shorter duration of stay in the work. Thus the positive correlation between age and BLL in the non-exposed group unlike in that of the exposed group seems to be reasonable. Similar positive correlation between BLL and age by the referent group was reported in the literature .
The American Conference of Governmental Industrial Hygienists (ACGIH) advises women of child-bearing age that if their BLL is >10 μg/dL, they are at risk of delivering a child with a BLL >10 μg/dL, which is the level of concern in the pediatric CDC guidelines . Although research findings have been inconsistent, the results of some recent investigations indicate that maternal BLL <10 μg/dL may be related to adverse reproductive outcomes, including preterm birth and spontaneous abortion [28, 29]. The fact that all the female construction workers and non-construction workers who participated in our study had BLLs >10 μg/dL and are in their most fertile age shows that they are parts of these risk groups.
The construction workers were found to exhibit significantly higher levels of the non-specific symptoms which included: memory impairment, headaches, wrist drop, nausea, and abdominal discomfort relative to the non-construction workers. Our report on the variations of the non-specific symptoms between the two groups is entirely from what the two groups revealed in the questionnaires and interviews. Although this may be suggestive of the adverse effects of lead on the exposed individuals relative to the unexposed, a close medical investigation is required to affirm that the epidemiologic variations between the two groups are exclusively results of the difference in the BLLs of the groups.
Our analysis might have been affected by several potential limitations of our study. Since confounding factors were not identified and controlled results of the various categories of the workers may be biased. In the workplace workers are not stationed to a specific working area. They move from places to place to help each other. Therefore, the BLL data corresponding to specific job types of workers may be biased because of such unrestricted movement. The sample sizes of both the occupationally exposed and unexposed cohorts might not be representative of the construction workers and the general population in Ethiopia. Similarly the female and male compositions in the two groups might not be representative of the two sexes to draw sex based conclusions. We had no records of environmental lead exposure in the proximity of the construction workers because monitoring of lead in air was not enforced in the country in general. As a result, any observed difference in response to occupational and environmental lead exposure may, therefore, be attributed to a degree of exposure to lead or different metabolic responses to lead in the construction workers. The participants in the control group were selected from boarding university students who have come from various rural and urban areas in the country where the exogenous lead exposures are different. As a result, any difference in BLL might not be attributed to the current living environment of the group. Moreover, absence of some epidemiological symptoms in this group might not be exclusively attributed to lower BLL relative to the construction workers.
This study has shown that unskilled construction workers are more likely exposed to lead than the general population. The BLLs determined are also high enough to call for an urgent measure. Infact more urgent is the case of females whose exposure is directly related with the health of their future babies. When we consider the literature reports on the association between: prenatal and postnatal blood lead concentrations with higher rates of total arrests and/or arrests for offenses involving violence, childhood lead exposure with region-specific reductions in adult gray matter volume, the inverse association of blood lead concentration in children with IQ, the issue goes beyond mother and child; extends to country level [30–32]. Mentally unhealthy and violent children would definitely harm the socio-economic development of the country and the peaceful life of the society.
The higher BLL determined in the unexposed group has also revealed that the general population including children is exposed to lead from different sources in the environment. The society in general, including most educated ones, is not aware about the dangers and routs of lead exposure and there is no BLL monitoring program in the country. As a result people do not protect themselves and their children from exposure to lead. Therefore, we call for a further large-scale screening and regular monitoring of occupationally exposed and unexposed workers to save the community from long term adverse effects of lead exposure.
The authors are grateful to Mr. Alexander Hayward for proofreading the manuscript and, to Dr. Nancy L. Pitts for her invaluable professional comments and proofreading the manuscript.
- Berode M, Wietlisbach V, Rickenbach M, Guillemin MP: Lifestyle and environmental factors as determinants of blood lead levels in a Swiss population. Environ Res 1991, 55: 1–17. 10.1016/S0013-9351(05)80136-7View ArticlePubMedGoogle Scholar
- Adela Y, Ambelu A, Tessema DA: Occupational lead Exposure among automotive garage workers – a case study for Jimma town, Ethiopia. J Occup med Toxicol 2012, 7: 5. available at http://www.occup-med.com/content/7/1/15 10.1186/1745-6673-7-5View ArticleGoogle Scholar
- Hense HW, Filipiak B, Novak L, Stoeppler M: Nonoccupational determinants of blood lead concentrations in a general population. Int J Epidemiol 1992, 21: 753–762. 10.1093/ije/21.4.753View ArticlePubMedGoogle Scholar
- Kaewboonchoo O, Morioka I, Saleekul S, Miya N, Chaikittiporn C, Kawa T: Blood lead level and cardiovascular risk factors among bus drivers in Bangkok, Thailand. Ind Health 2010, 48: 61–65. 10.2486/indhealth.48.61View ArticlePubMedGoogle Scholar
- Pocock SJ, Shaper AG, Walker M, Wale CJ, Clayton B, Delves T, Lacey RF, Packham RF, Powell P: Effects of tap water lead, water hardness, alcohol, and cigarettes on blood lead concentrations. J Epidemiol Community Health 1983, 37: 1–7. 10.1136/jech.37.1.1PubMed CentralView ArticlePubMedGoogle Scholar
- Rhainds M, Levallois P: Effects of maternal cigarette smoking and alcohol consumption on blood lead levels of newborns. Am J Epidemiol 1997, 145: 250–257. 10.1093/oxfordjournals.aje.a009098View ArticlePubMedGoogle Scholar
- Shaper AG, Pocock SJ, Walker M, Wale CJ, Clayton B, Delves HT, Hinks L: Effects of alcohol and smoking on blood lead in middle-aged British men. Br Med J 1982, 284: 299–302. 10.1136/bmj.284.6312.299View ArticleGoogle Scholar
- Popovic M, McNeill FE, Chettle DR, Webber CE, Lee CV, Kaye WE: Impact of occupational exposure on lead levels in women. Environ Health Perspect 2005, 113: 478–484. 10.1289/ehp.7386PubMed CentralView ArticlePubMedGoogle Scholar
- National Health and Medical Research Council (NHMRC): Blood lead levels for Australians: An information paper for practitioners and policy makers, Australian Government, Canberra. S.Google Scholar
- Occupational Safety and Health Administration (OSHA): Lead in construction. United States Department of Labor 2003. 3142–09R. 200 Constitution Avenue, NW, N-3101, Washington, DC 20210;Google Scholar
- Roscoe RJ, Ball W, Curran JJ, DeLaurier C, Falken MC, Fitchett R, Fleissner ML, Fletcher AE, Garman SJ, Gergely RM, Gerwel BT, Gostin JE, Keyvan-Larijani E, Leiker RD, Lofgren JP, Nelson DR, Payne SF, Rabin RA, Salzman DL, Schaller KE, Sims AS, Smith JD, Socie EM, Stoeckel M, Stone RR, Whittaker SG: Adult blood lead epidemiology and surveillance - United States, 1998–2001. CDC MMWR Surveill Summ 2002, 51: 1–10.PubMedGoogle Scholar
- Needleman HL, Landrigan PJ: What level of lead in blood is toxic for a child? Am J Public Health 2004, 94: 8. 10.2105/AJPH.94.1.8PubMed CentralView ArticlePubMedGoogle Scholar
- United States Department of Labor, Occupational Safety and Health Administration: Lead exposure in construction - interim rule. Fed Regist 2004, 58: 26590–26649. [29 CFR § 1926.62]Google Scholar
- Agency for Toxic Substances and Disease Registry (ATSDR): Toxicological profile for lead. Atlanta, GA: US Department of Health and Human Services, Public Health Service; 2005.Google Scholar
- Ahmed K, Ayana G, Engidawork E: Lead exposure study among workers in lead acid battery repair units of transport service enterprises, Addis Ababa, Ethiopia: a cross-sectional study. J Occup Med Toxicol 2005, 3: 30. doi:10.1186/1745–6673–3-30View ArticleGoogle Scholar
- Sackett H, Mulloy KB, Newman L: Occupational Health Indicators in Colorado: A Baseline Health Assessment (2001–2005). Colorado School of Public Health, October 1, 2008;Google Scholar
- United Nations Environment Programme (UNEP) and United Nations Children’s Fund (UNICEF): Childhood lead poisoning: Information for advocacy and action. UNICEF, 3 UN Plaza, New York, NY 10017, USA: UNEP, Nairobi, Kenya; 1997.Google Scholar
- Menke A, Muntner P, Batuman V, Silbergeld EK, Guallar E: Blood lead below 0.48 mmol/L (10 mg/dL) and mortality among US adults. Circulation 2006, 114: 1388–1394. 10.1161/CIRCULATIONAHA.106.628321View ArticlePubMedGoogle Scholar
- Miranda ML, Kim D, Reiter J, Overstreet GMA, Maxson P: Environmental contributors to the achievement gap. Neurotoxicology 2009, 30: 1019–1024. 10.1016/j.neuro.2009.07.012PubMed CentralView ArticlePubMedGoogle Scholar
- Vigeh M, Yokoyama K, Seyedaghamiri Z, Shinohara A, Matsukawa T, Chiba M, Yunesian M: Blood lead at currently acceptable levels may cause preterm labour. Occup Environ Med 2011, 68: 231–234. 10.1136/oem.2009.050419View ArticlePubMedGoogle Scholar
- Fatoki OS, Ayoade D: Lead assay in blood of occupationally and non-occupationally exposed donors. Int J Environ Heal R 1996, 6: 195–200. 10.1080/09603129609356890View ArticleGoogle Scholar
- Njoroge GK, Njagi ENM, Orinda GO, Sekadde-Kigondu CB, Kayima JK: Environmental and occupational exposure to lead. East Afr Med J 2008, 85: 284–291.View ArticlePubMedGoogle Scholar
- Aliasgharpour M, Hagani H: Impact of occupational lead exposure on industrial workers health condition in Tehran-Iran. Eastern J Med 2005, 10: 20–23.Google Scholar
- Rabin R, Brooks DR, Davis LK: Elevated blood lead levels among construction workers in the Massachusetts occupational lead registry. Am J Public Health 1994, 84: 1483–1485. 10.2105/AJPH.84.9.1483PubMed CentralView ArticlePubMedGoogle Scholar
- Bener A, Almehdi AM, Alwash R, Al-Neamy FRM: A pilot survey of blood lead levels in various types of workers in the United Arab Emirates. Environ Int 2001, 27: 311–314. 10.1016/S0160-4120(01)00061-7View ArticlePubMedGoogle Scholar
- Yakub M, Iqbal MP: Association of blood Lead (Pb) and plasma homocysteine: a cross sectional survey in Karachi, Pakistan. PLoS ONE 2010, 5: 1–6.View ArticleGoogle Scholar
- American Conference of Governmental Industrial Hygienists. TLVs and BEIs: Threshold limit values for chemical substances and physical agents and biological exposure indices. Cincinnati: OH: ACGIH; 2001.Google Scholar
- Borja-Aburto VH, Hertz-Picciotto I, Rojas LM: Blood lead levels measured prospectively and the risk of spontaneous abortion. Am J Epidemiol 1999, 50: 590–597.View ArticleGoogle Scholar
- Torres-Sanchez LE, Berkowitz G, Lopez-Carrillo L: Intrauterine lead exposure and preterm birth. Environ Res 1999, 81: 294–301.View ArticleGoogle Scholar
- Wright JP, Dietrich KN, Ris MD, Hornung RW, Wessel SD, Lanphear BP, Ho M, Rae MN: Association of prenatal and childhood blood lead concentrations with criminal arrests in early adulthood. PLoS Med 2008, 5: 0732–0740.View ArticleGoogle Scholar
- Cecil KM, Brubaker CJ, Adler CM, Dietrich KN, Altaye M, Egelhoff JC, Wessel S, Elangovan I, Hornung R, Jarvis K, Lanphear BP: Decreased brain volume in adults with childhood lead exposure. PLoS Med 2008, 5: 0741–0750.View ArticleGoogle Scholar
- Canfield RL, Henderson CR, Cory-Sletchta DA, Cox C, Jusko TA, Lanphear BP: Intellectual impairment in children with blood lead concentrations below 10 μg/decilitre. N Engl J Med 2003, 348: 1517–1526. 10.1056/NEJMoa022848PubMed CentralView ArticlePubMedGoogle Scholar
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