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Indian Pediatr 2015;52:
305-306 |
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Blood Lead Levels and Childhood Asthma
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Ahmed Abdullah Mohammed, Faisal Yosef Mohamed, *El-Sayed
El-Okda and Adel Besheer Ahmed
From the Departments of Pediatrics and *Community
medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Correspondence to: Dr Ahmed Abdullah Mohammed,
Assistant Professor of Pediatrics, Ain Shams University, Faculty of
Medicine, Abbassia, Cairo Egypt. PO Box 11566.
Email: [email protected]
Received: September 1, 2014;
Initial review: October 21, 2014;
Accepted: January 12, 2015.
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Objective: To measure blood lead levels
in children (5-14 y) with bronchial asthma, and correlate with asthma
severity.
Design: Cross-sectional
analytical.
Setting: Pediatric Allergy and
Immunology Clinic of a Children’s hospital in Cairo, Egypt.
Participants: 200 children (127
males) with bronchial asthma and125 age- and sex-matched healthy
controls (80 males).
Procedure: Blood lead levels were
measured by atomic absorption spectrophotometer technique, and were
subsequently correlated with asthma severity.
Results: No significant
difference in mean (SD) blood lead levels was observed between children
with asthma [13.3 (4.8) µg/dL] and control group [11.4 (3.9) µg/dL]. 190
children (58.5%) had elevated blood lead levels (>10 µg/dL), with no
significant difference between patients (60%) and controls (56%).
Patients with elevated blood lead levels had significantly higher
frequency of eosinophilia (66.7%) and increased total immunoglobulin E
(83.3%) compared to other patients with blood lead levels <10 ìg/dL (10%
and 43.8%, respectively). Patients of asthma with elevated blood lead
levels had higher grades of severity of asthma compared to those with
blood lead levels <10 µg/dL.
Conclusions: Blood lead levels
are not significantly associated with diagnosis of asthma but elevated
blood lead levels seem to be associated with increased asthma severity
and higher frequency of eosinophilia and elevated immunoglobulin E
levels.
Keywords: Bronchial asthma, Eosinophilia, Lead
poisoning, Risk factors.
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L ead poisoning and asthma are common pediatric
health problems. Both diseases have environmental mechanisms and some
risk factors for both diseases are similar. Lead paints are a primary
source for lead poisoning [1], and there is evidence that exposure to
household allergens increases asthma morbidity [2]. Household dust is an
important source for both lead and allergens [3]. Lead exposure alters
immune system components and is associated with increased production of
immunoglobulin E (IgE) [4]; it also depresses the activity of several
enzyme systems that influence cellular reducing capacity and
consequently may increase asthma risk [5].
We hypothesized that exposure to lead is one of the
environmental risk factors for bronchial asthma among children living in
urban overcrowded areas. This study was designed to measure the blood
lead level (BLL) among a sample of children with asthma living in an
urban slum area, and to correlate it with asthma severity.
Methods
This observational, cross-sectional study was
conducted at the Pediatric Allergy and Immunology Clinic, Ain Shams
University, Children’s Hospital, Cairo, Egypt, during the period May
2011 to October 2012. This clinic serves infants and children in
Abbassia (lower-middle-class urban district in Cairo). The study was
approved by the Ethical Committee of the Pediatrics Department, Faculty
of Medicine, Ain Shams University. An informed consent was obtained from
the parents or caregivers of each child before enrolment in the study.
The patient group included 200 children (127 males)
aged 5-14 years, with bronchial asthma diagnosed clinicaly according to
GINA (2010) criteria (clinical symptoms of episodic wheezing,
chest tightness and dyspnea that improved at least partially after
bronchodilator therapy [6]. Asthma severity was classified according to
the National Asthma Education and Prevention Program, 2007 [7].
One hundred and twenty-five apparently healthy
children males) without personal or family history of asthma or other
atopic conditions (atopic dermatitis, allergic rhinitis or allergic
conjunctivitis) were included as controls. They were recruited from the
outpatient clinic among those attending for preoperative assessment for
elective surgeries such as tonsillectomy and adenoidectomy. A part of
the blood sample collected for pre-operative assessment of controls was
used for the study. Written informed consent was obtained from parents
or guardians who accepted to participate in the study. We excluded
patients and controls with other respiratory diseases.
Socio-demographic information included age, gender,
parents’ education, parents’ occupation and parental smoking. Parents’
education was graded as non-educated (illiterate), under-moderate
(primary or preparatory education), moderate (secondary education) and
high (university graduation or postgraduate). Environmental and
behavioral factors included parental smoking, eating canned food,
drinking canned juice, putting colored toys in the mouth, using colored
pencils, use of toothpaste, and use of newspapers in food preparation
wrapping, preserving, or as table mats. Chest examination was
performed to assess degree of clinical severity and to exclude acute
respiratory infection. In all subjects, 3 mL of venous blood was
collected. The blood count was performed using the Coulter counter
(Coulter micro DIFF 18, CA, USA). The differential leukocyte counts were
estimated manually from the blood film and expressed in absolute count
values. Eosinophilia was considered when the absolute eosinophil counts
exceeded the normal reference values for age [8]. Serum total
immunoglobulin E (IgE) was measured by quantitative enzyme immunoassay (Biocheck,
Inc 323 Vintage Park Dr. Foster City, CA 94404) based on solid phase
ELISA. Total IgE was considered high when it exceeded the upper limit of
the normal range for age (60 IU /mL for children younger than 6 years,
90 IU /mL for 6-8 years and 200 IU /mL for children older than 8 years)
[9]. Blood lead level (BLL) was measured by atomic absorption
spectrophotometer technique [10]. According to the Centers for Disease
Control and Prevention, elevated BLL was considered when it was >10 µg/dL
[1].
Statistical Analyses: The data were coded
and analyzed with the Statistical Package for Social Sciences (version
20; SPSS Inc, Chicago, III). Student t test was used for parametric
quantitative variables, and chi-square test was used to compare
frequency of qualitative variables among the different groups. Backward
likelihood ratio technique for binary logistic regression model was used
to find out independent predictors of elevated BLL. The covariates
included in the regression model were parental smoking, eating canned
food, drinking canned juice, putting colored toys in the mouth, using
colored pencils, use of toothpaste and use of newspapers for handling
food. For all analyses, the level of significance was set at P<
0.05.
Results
One hundred and ninety children (58.5%) had elevated
BLL (BLL ³10
ug/dL), with no significant difference between patients (60%) and
control group (56%) (Table I). Patients with elevated BLL
had significant increase in the severity of asthma, higher frequency of
eosinophilia, and higher total IgE compared to other patients with BLL
below 10 µg/dL (Table II).
TABLE I Comparisons Between Children with Asthma and Control Group Regarding Different Variables
Variable |
Asthma |
Controls |
P |
|
(n=200) |
(n=125) |
|
Age (in years) |
7.4 (3.5) |
7.4 (2.3) |
0.460 |
BLL (ug/dL) |
13.3 (4.8) |
11.4 (3.9) |
0.191 |
#Gender: Male |
127 (63.5) |
80 (64 ) |
0.675 |
#Parental Smoking |
93 (46.5) |
38 (30.4) |
0.233 |
*#High BLL |
120 (60) |
70 (56) |
0.582 |
BLL: blood lead level.*High BLL was considered above 10 mg/dL
Values in mean (SD) or #No. (%). |
TABLE II Asthma Severity Parameters and Blood Lead Levels in Study Subjects [No. (%)].
Variable |
BLL >10mg/dL |
BLL<10mg/dL |
P |
|
(n = 120) |
(n = 80) |
|
Severity of asthma |
|
|
|
Mild intermittent |
24 (40) |
36 (60) |
0.021 |
Mild persistent |
54 (60) |
36 (40) |
|
Moderate persistent |
28(82.4) |
6 (17.6) |
|
Severe persistent |
14(87.5) |
2 (12.5) |
|
Eosinophilia |
80(66.7) |
8 (10) |
<0.001 |
High total IgE |
100(83.3) |
35 (43.8) |
<0.001 |
Regarding sociodemographic risk factors for elevated
BLL among all studied children, low mother’s education and low father’s
education were significantly associated with elevated BLL. Gender,
mother’s occupation and father’s occupation were not associated with
elevated BLL (Table III).
TABLE III Socio-demographic and Other Risk Factors for Elevated BLL Among all Studied Children
Risk factors |
BLL≥10mg/dL |
BLL<10mg/dL |
P |
|
N = 190 |
N = 135 |
|
Mother’s education |
Non educated (42)
|
37(88.1) |
5 (11.9) |
< 0.001 |
High (85)
|
35 (41.2) |
50 (58.8) |
|
Father’s education |
Non educated (40)
|
33 (82.5) |
7 (17.5) |
|
High (85)
|
30(35.3) |
55 (64.7) |
|
Parental smoking (175) |
120 (68.6%) |
55 (31.4%) |
0.032 |
Putting colored toys in mouth (230) |
175 (70.1%) |
55 (23.9%) |
<0.001 |
Using colored pencils (287) |
182 (63.5%) |
105(36.5%) |
<0.001 |
Eating canned food (277) |
182 (65.7) |
95 (34.3) |
<0.001 |
Use of newspapers |
During food preparation (195)
|
150 (76.9) |
45 (23.1) |
<0.001 |
In wrapping & pre-serving food (140)
|
110 (78.6) |
30 (21.4) |
<0.001 |
Parental smoking, putting colored toys in the mouth,
using colored pencils, eating canned food, use of newspapers for
handling food and use of toothpaste were associated with elevated BLL (Table
III).
Discussion
In this study, we found that elevated BLL among
patients with asthma was associated with higher frequency of
eosinophilia and increased total IgE, and with a significant increase in
the severity of asthma compared to the patients with asthma with BLL
<10µg/dL.
Previous studies have suggested that lead exposure
alters immune system components and is associated with many steps in the
pathophysiology of increased bronchial hyper-responsiveness [11-14]. The
relatively higher frequency of elevated BLL in our study compared to the
previous studies done in Cairo, Egypt [15,16] can be explained by
recruitment of children from high risk areas for lead contamination in
our study.
In our study, we did not find a significant
difference between patients and control group regarding the mean BLL.
Previous researchers have also reported that elevated BLL and chronic
exposure to lead was not associated with the risk of developing asthma
[17,18]. On the other hand, association between exposure to lead and
bronchial asthma was demonstrated by some studies [4,19,20]. The young
age of included children and high frequency of elevated BLL among
studied population may explain the inconsistency between our results and
results of these studies.
Our study has some limitations. As a cross sectional
study, the BLL is primarily an indicator of recent exposure. For
environmental risk factors, the study relied on reporting by parents;
the specific products and environments were not directly tested for
presence of lead.
In conclusion, although elevated BLL had no
significant correlation with asthma diagnosis, it was significantly
associated with increased asthma severity.
Contributors: AAM, FYM, ABA: conceived the study
design, collected and analyzed the data; EEE: performed the statistical
data analysis; AAM: wrote the manuscript and revised it critically for
important intellectual content. All authors have read and approved the
final manuscript.
Funding: None; Competing interests: None
stated.
What is Already Known?
•
Lead poisoning and asthma are affected by the environment
and substandard housing conditions.
What This Study Adds?
•
Elevated BLL (≥10
µg/dL) is significantly associated with increased severity of
childhood asthma.
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