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Research | Children's Health
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| The Association between Phthalates in Dust
and Allergic Diseases among Bulgarian Children Barbara Kolarik,1,2 Kiril Naydenov,1,3 Malin Larsson,4 Carl-Gustaf Bornehag,1,4,5 and Jan Sundell1 1Technical
University of Denmark, Department of Mechanical Engineering,
International Centre for Indoor Environment and Energy, Lyngby,
Denmark; 2Silesian University of Technology, Faculty of
Environmental Engineering and Energy, Gliwice, Poland; 3Birch & Krogboe
A/S, Virum, Denmark; 4Public Health Sciences, Karlstad University,
Karlstad, Sweden; 5SP-Technical Research Institute of Sweden,
Boras, Sweden Abstract Background: Recent studies have identified associations between the concentration of phthalates in indoor dust and allergic symptoms in the airways, nose, and skin. Objectives: Our goal was to investigate the associations between allergic symptoms in children and the concentration of phthalate esters in settled dust collected from children's homes in Sofia and Burgas, Bulgaria. Methods: Dust samples from the child's bedroom were collected. A total of 102 children (2–7 years of age) had symptoms of wheezing, rhinitis, and/or eczema in preceding 12 months (cases) ,and 82 were nonsymptomatic (controls) . The dust samples were analyzed for their content of dimethyl phthalate (DMP) , diethyl phthalate (DEP) , di-n-butyl phthalate (DnBP) , butyl benzyl phthalate (BBzP) , di(2-ethylhexyl) phthalate (DEHP) , and di-n-octyl phthalate (DnOP) . Results: A higher concentration of DEHP was found in homes of case children than in those of controls (1.24 vs. 0.86 mg/g dust) . The concentration of DEHP was significantly associated with wheezing in the preceding 12 months (p = 0.035) as reported by parents. We found a dose–response relationship between DEHP concentration and case status and between DEHP concentration and wheezing in the preceding 12 months. Conclusions: This study showsan association between concentration of DEHP in indoor dust and wheezing among preschool children in Bulgaria. Key words: allergy, asthma, children, DEHP, phthalates. Environ Health Perspect 116:98–103 (2008) . doi:10.1289/ehp.10498 available via http://dx.doi.org/ [Online 15 October 2007] Address correspondence to B. Kolarik, Silesian University of Technology, Faculty of Environmental Engineering and Energy, ISE, OWiTO, Konarskiego 18, 44-100 Gliwice, Poland. Telephone: (004832) 237 23 95. Fax: (004832) 237 25 59. E-mail: bf@mek.dtu.dk We gratefully acknowledge D.P. Wyon for revising the language. This work was supported by the Danish Technical Research Council (STVF) as part of the research program of the International Centre for Indoor Environment and Energy established at the Technical University of Denmark for 1998–2007. B.K. was additionally supported by the scholarship from International Visegrad Fund, Bratislava, Slovak Republic, for 2005–2006. The authors declare they have no competing financial interests. Received 24 May 2007 ; accepted 15 October 2007. |
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In the developed parts of the world, people
spend ≥ 90% of their life indoors (Brasche and Bischof
2005), which implies that indoor environmental conditions are
important for people's health. Indoors, pollutants in
dust and air are often generated from sources such as
environmental tobacco smoke, building materials, furniture,
cleaning and hygienic products, air fresheners, computers,
printers, cooking and other indoor activities, and from people
themselves.
Over the last few decades,
asthma and allergies have increased all over the world [Asher
et al. 2006;
ISAAC (International Study of Asthma and Allergy in Childhood)
Steering Committee 1998; World Health Organization 2003]. The
causes of the increase in asthma and allergies are still
unknown. Genetic changes are not believed to be important
because the time interval (30–50 years) for the
increase in allergies is far too short. Instead, environmental
changes are suspected as possible causes. Several hypotheses
have been put forward. Much interest has been focused on the so
called "hygiene hypothesis"—that a lack of
microbial exposure during critical periods in infancy increases
the risk of allergies (Strachan 1989). However, it seems likely
that this hypothesis may not be the sole cause, and that other
hypotheses are required (Platts-Mills et al. 2005). One such
hypothesis is that the increase in allergies is attributable
to new adjuvant factors: exposure to environmental pollutants
such
as endocrine disruptors (e.g., phthalate esters) which may act
as modulators of the immune system and induce an allergic
response (Chalubinski and Kowalski 2006).
One of the main sources
for phthalate esters indoors is the plasticized polyvinyl chloride
(PVC)
materials (Bornehag et al. 2005a) that are used in floor and
wall covering materials, shower curtains, adhesives, synthetic
leather, toys, cosmetics, and many other consumer products.
Phthalates are constantly being emitted to the air and indoor
dust because they are not chemically bound to the PVC
structure (Wormuth et al. 2006).
The presence of phthalates
in indoor dust (Becker et al. 2004; Bornehag et al. 2004; Butte
et al. 2001;
Clausen et al. 2003; Fromme et al. 2004; Kersten and Reich
2003; Oie et al. 1997; Pohner et al. 1997; Rudel et al. 2003)
and in indoor air (Adibi et al. 2003; Fromme et al. 2004; Rudel
et al. 2003) is well documented. In the literature, the
predominant phthalate described in indoor dust is
di(2-ethylhexyl) phthalate (DEHP), typically observed in a
concentration range of 0.01–10 mg/g dust, followed
by butyl benzyl phthalate (BBzP) in concentrations up to 1.3
mg/g
dust. The phthalate concentration in indoor air is usually
lower than the concentration in dust, and the predominant
phthalates are diethyl phthalate (DEP) and di-n-butyl
phthalate (DnBP) in the concentration range of 0.05–5 µg/m3. Human
exposure to phthalates has been studied mainly by monitoring
concentrations of metabolites in body fluids such as urine or
blood (Adibi et al. 2003; Becker et al. 2004; Blount et al.
2000; Calafat et al. 2004; Green et al. 2005; Koch et al. 2003,
2005). The results have shown that people are exposed to
multiple phthalates and that children often are more exposed
than adults (Calafat et al. 2004; Green et al. 2005; Koch et al.
2005).
There is some epidemiologic
evidence for an association between the concentration of phthalates
in indoor
dust and/or the occurrence indoors of plasticized products such
as PVC and allergic symptoms in the airways (e.g., asthma),
nose, and skin. Jaakkola et al. (1999) found that the total
area of PVC surface materials in homes was associated with the
development of bronchial obstruction in small children in
Norway. In a study from Finland (Jaakkola et al. 2000), lower
respiratory tract symptoms in children such as persistent
wheezing, cough, and phlegm were associated with the presence
of plastic wall materials, whereas upper respiratory tract
symptoms were not. Also, the relative risk estimated for
pneumonia, bronchitis, and otitis media among children was
slightly increased in the presence of plastic wall materials
(Jaakkola et al. 2000). In a population-based incident
case–control study among adults (21–63 years of
age), Jaakkola et al. (2006) found that the risk of asthma was
significantly related to the presence of plastic wall materials
at work.
In the first phase of the
Swedish DBH (Dampness in Buildings and Health) study it was found
that PVC
as flooring material in combination with moisture problems in
the floors was associated with asthma among children 1–6
years of age (Bornehag et al. 2005b). Furthermore, in the
second phase of the DBH study a strong dose–response
relationship was found between asthma among children and DEHP
concentration in indoor dust and between eczema and rhinitis
and BBzP (Bornehag et al. 2004). Oie et al. (1997) provided
evidence that inhalation exposure to DEHP as aerosols adsorbed
to particulate matter is even more important than vapor phase
exposure. They discussed possible mechanisms for respiratory
effects by inhalation exposure and concluded that deposition
of DEHP in the lungs may increase the risk of inflammation in
the
airways, a characteristic feature of asthma.
The results from toxicologic studies are
conflicting. Lee et al. (2004) reported that DEHP and
di-isononyl phthalate (DINP) enhance allergic responses by
enhancement of interleukin (IL)-4 production in CD4+ T
cells via stimulation of NF-AT (nuclear factor of activated T
cells)–binding activity. Glue et al. (2005) investigated
the effect of phthalates to modulate the release of histamine
from isolated basophils. None of the phthalates tested was
found to induce histamine release per se, but higher histamine
release was observed when the cells were first treated with
phthalates and then exposed to an allergen. Recently, Larsen
et al. (2007) reported that long-term inhalation of DEHP together
with an allergen resulted in allergy sensitization only in
concentrations of 13 mg/m3. These authors concluded
that DEHP, at realistic concentrations, does not cause adjuvant
effects nor allergic
lung inflammation in humans. In a recent review, Nielsen et al.
(2007) concluded that results from animal and epidemiologic studies
are discordant.
This study (The ALLHOME study) was
initiated in Bulgaria in 2004. The overall aim of the study was
to map housing conditions and indoor exposures in Bulgaria
and
to investigate the role of such factors for allergies and
asthma among small children (Naydenov 2007; Naydenov et al.
2005).
Our main aim in the present article
is to investigate associations between persistent allergic
symptoms in preschool Bulgarian children and the concentrations
of different phthalate esters in dust collected from the
children's bedrooms.
The ALLHOME study is divided
into two phases: a cross-sectional questionnaire study (ALLHOME-1)
and
a nested case–control study (ALLHOME-2), including dwelling
inspections, exposure measurements, and medical examinations.
The ALLHOME study was designed to be a twin study to the
Swedish DBH study (Bornehag et al. 2004; Naydenov 2007).
From April 2004 to August
2004 a baseline questionnaire (ALLHOME-1) on housing and health
was sent to the
parents of all children 2, 3, 5, and 7 years of age living in
selected districts of Sofia and Burgas, Bulgarian cities with
populations of about 1.2 million and 0.2 million, respectively.
Data for 4,479 children was collected, corresponding to a
response rate of 34.5%. Based on reported symptoms in the
ALLHOME-1 study, potential case and control children in the
ALLHOME-2 study were selected (Naydenov 2007). Potential cases
were all children who were reported to have at least two of the
following three symptoms in the ALLHOME-1 study: "wheezing during the last 12 months,"
"rhinitis during the last 12 months, when not having a
cold," and "itching rash eczema in the last 12
months." The potential controls were all children who
reported an absence of all three symptoms stated above as well
as absence of "wheezing ever in the past,"
"dry cough more than 2 weeks, without a cold,"
"diagnosed asthma by a doctor ever in the past,"
"running nose ever in the past without cold/flu,"
"running nose or watering eyes on pet contact in the last
12 months," "running nose or watering eyes on
pollen contact in the last 12 months," "diagnosed
hay fever by a doctor ever in the past," and
"itching rash ever in the past lasting more than 6 months
in typical locations of the child's body." No
matching of cases or controls was carried out.
Of 4,479 children, 2,105 met the inclusion
criteria for cases and controls: 730 (16.3%) were potential
cases and 1,375 (30.7%) were potential controls. In a follow-up
questionnaire study (3 months later), parents of both cases
and
controls had to agree to participate, had to have not rebuilt
their house because of moisture problems, and had to have not
changed home during the time between the baseline and follow-up
questionnaire. Furthermore, invited case children had to have
at least one of the three symptoms (wheezing, rhinitis,
eczema), and invited controls had to be free from the symptoms
listed in the follow-up questionnaire. The selection procedure
identified a total of 272 children (136 cases and 136 controls)
(Naydenov 2007).
Exposure measurements in
the homes and health examinations of the case and control children
were
conducted from December 2004 to March 2005. Despite their
written consent given in the follow-up study, the parents of
56 children refused to have their home inspected. Home
investigations were therefore performed in 209 homes of 216
children because there were seven pairs of siblings. In 26 of
the inspected homes, inspectors were not allowed to perform
dust sampling; thus dust samples from only 183 homes of 190 children
were collected. Six samples were either inadvertently destroyed
in the laboratory or not coded by inspectors. As a result, dust
samples from 177 homes of 184 children, including 102
cases and 82 controls, were available for analysis.
Table 1.

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Table 2.

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Table 3.

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Table 4.

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Table 5.

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Sampling of settled
dust was performed in the child's room, above the floor level, such as over the
door and from shelves and frames of paintings. A 1,600-W vacuum
cleaner equipped with a phthalate-free ALK dust sampling device
(ALK dust collector and filter; ALK-Abelló A/S,
Hørsholm, Denmark) was used for the dust collection. The
dust samples were wrapped in aluminum foil and kept in a
polyethylene bag with a zip lock, so that the dust had no
contact with the bag. Samples were frozen the day of sampling
at –18°C. They were later thawed to room temperature
and sent to a laboratory. The dust was not sieved, but the
filter used retained 74% of particles 0.3–0.5 µm,
81% of particles 0.5–1.0 µm, 95% of particles
1–10 µm, and 100% of larger particles (ISAAC 1998).
The filters were not weighed before the sampling took place,
but the dust was weighed before analysis at room temperature.
The phthalate concentrations are expressed as a fraction of the
dust that could be shaken out of the filter. Dust samples were
extracted in 2-mL glass vials for 1 hr using 1 mL of 10%
toluene solution in carbon disulfide. Two milliliters of this
solution was injected into a capillary column (Hewlett Packard
DB-5 capillary column, H-30 m, 0.53 mm diameter). The column
temperature started at 80°C for 5 min and then increased at
20°C/min to 290°C, which was maintained for 10 min. The
technique used for the analysis was gas chromatography/flame
ionization detection, which is used for qualitative
identification and quantitative determination. In this method,
components separated in the gas chromatograph pass through the
flame, burn, and produce ions, with a current that is
proportional to the amount of hydrocarbons in the sample. Six
phthalates were analyzed: dimethyl phthalate (DMP), DEP, DnBP,
BBzP, DEHP, and di-n-octyl phthalate (DnOP). The detection
limits, in milligrams of phthalate per gram of dust (for median
dust
weight), was in the range of 0.06–0.26 mg/g, depending
on the type of phthalate. DEHP and DnBP were found in all analyzed
samples. For other phthalates, the percent of nondetects is
given in Table 2.
Statistical analysis. The analyses
of concentrations of phthalates in dust and building characteristics
were made for all 177 homes
visited. The concentrations of phthalates were not normally
distributed. The concentrations are reported as medians,
arithmetic means, and geometric means (GM) with 95% confidence
intervals (CI) where the CI was calculated with a
back-transform of mean log ± 2 x SE.
Ranges of concentrations of measured phthalates are also presented.
We analyzed potential associations between concentration
of phthalates and health outcomes using the nonparametric
Mann-Whitney U-test and one-way analysis of variance and
Dunnett's test (on log-transformed data). Dunnett's
test controls for family-wise error rate (which is the
probability of making false discoveries, or type I errors among
all the hypotheses when performing multiple pair-wise tests)
and can be used for multiple comparisons, when comparing with
controls.
We tested dose–response relationships
using the phthalate concentrations in quartiles and using both
uni- and multivariate logistic regression analyses. We tested
dose–response relationships with a trend test. Results
are presented as crude and adjusted odds ratios (ORs) with 95%
CIs. In all multivariate analyses, adjustments were made for
age (< 3 years vs. ≥ 5 years of age), sex (male vs.
female), smoking during pregnancy and first year of child's life (any
parents smoking in the house during the pregnancy and first
year of the child's life vs. no smoking in the home),
current smoking at home (one or more occupants currently
smoking in the house vs. no smoking) and allergy and/or asthma
symptoms in the family (at least one symptomatic family member
other than the index child vs. no other person with symptoms).
Because all the included siblings (n = 7) had separate
rooms and the separate dust samples had been collected for each
of them, the analyses
of association between phthalates and health were made for 184
children. Additional analyses, limited to one child per
household (selected based on lower identification number) were
also performed.
All analyses were made by using SPSS 15.0
for Windows (SPSS Inc., Chicago, IL, USA).
The study was approved by the local ethics
review board. Parents gave written informed consent to the
participation of their children in the study.
The study group consisted
of 96 boys and 88 girls, 105 of them < 3 years of age. Nine families lived in
single-family houses, the rest in multifamily houses, and 131
(75%) of the houses were built in 1960–1990. All
buildings had natural ventilation, and 40% had a kitchen
exhaust hood with a fan. Table 1 shows selected
demographic, building and family routine characteristics.
Phthalates in dust.Geometric
mean phthalate concentrations with 95% CIs, in milligrams of phthalate
per
gram of dust, are shown in Table 2. For most of the
samples analyzed, phthalates were above the detection limits.
DEHP and DnBP were found in all collected samples.
Associations between concentrations of phthalates
in dust and health status of the children.Median
and arithmetic mean phthalate concentrations for case and control
children are
presented in Table 3. In general, there were no
differences in the concentration of most phthalates in dust
between homes of cases and controls. However, DEHP was found
in higher concentrations in the homes of cases than in controls.
Furthermore, case children with reported wheezing in the
preceding 12 months had significantly higher concentrations of
DEHP than controls. The concentration of BBzP was higher in the
homes of children with wheezing and eczema (both in the
preceding 12 months), though not significantly higher.
A significant dose–response
relationship was observed between the concentration of DEHP in
indoor dust and case status, and between DEHP and current
wheezing (Table 4).
In Bulgaria, PVC and linoleum floor
materials are sold under the common name balatum,
which makes it impossible to distinguish reliably between them
based on
information obtained from parental questionnaires or
inspectors' notes. However, the presence of balatum in
the child's bedroom, as reported by inspectors, was
significantly associated with case status among the children
(adjusted OR = 2.21; 95% CI, 1.13–4.32). A
significant association was also found between balatum (as
reported by inspectors) and both wheezing (adjusted OR = 2.64;
95% CI, 1.34–5.21) and rhinitis in preceding 12
months (adjusted OR = 2.15; 95% CI, 1.08–4.17).
The same results were obtained for the presence of balatum as reported
by parents in the main questionnaire and health effects. There
was no association between concentration of phthalates in dust
and the presence of balatum flooring.
Polishing products,
used when dusting the furniture, were found to be a strong source
of phthalates in
Bulgaria. The use of polishing products in the home (at least
once per month compared with no use or very rare use), as
reported by parents, was associated with case status (adjusted
OR = 1.75; 95% CI, 0.95–3.23), wheezing in the preceding
12 months (adjusted OR = 1.92; 95% CI, 1.02–3.62),
and rhinitis in the preceding 12 months (adjusted OR = 1.71;
95% CI, 0.90–3.23). The use of polishing products
was also significantly associated with the concentration of
BBzP (p =
0.025) and DnOP (p = 0.040) in indoor dust. Concentrations of DEP
and DEHP were also higher, though not significantly higher, in
homes where such products were used. A high frequency of
cleaning (dusting) of furniture was associated with fewer
health problems (as defined by case status and by all three
symptoms) but with concentration of BBzP, which was
significantly higher in homes that were cleaned less often (p =
0.007).
The concentration
of DEHP in indoor dust was in about the same concentration range
as in several other
studies, including the Swedish DBH study (Bornehag et al. 2004)
(Table 5). The concentration of BBzP was found in somewhat
higher concentration in Bulgaria compared with other studies.
Large differences were observed for DnBP, which was found in
concentrations up to 40 times higher in Bulgaria than in other
countries (Table 5), and for DEP and DMP, which were also
found in much higher concentrations in the present study than
in other studies (Bornehag et al. 2004; Fromme et al. 2004).
None of the main sources identified (balatum flooring,
polishing products) were correlated with the concentration of
DnBP, and only a slight, nonsignificant correlation was found
between DEP and use of polishing products. No information on
other possible sources of these phthalates (e.g. cosmetics,
soft toys, plastic covers on furniture) was obtained, so we are
unable to put forward any hypotheses that might explain the
high concentrations of DnBP and DEP that were found in this
study.
The results support the
finding from the Swedish DBH study regarding an association between
DEHP and
asthmatic and allergic symptoms among children (Bornehag
et al. 2004). Although the Swedish findings regarding an
association of the dust concentration of BBzP with rhinitis and
eczema were not replicated in a significant manner in the
current study, the results from Bulgaria point to the same
conclusion as in Sweden.
In the present study, each child was
treated as separate observation, because in homes with multiple
children participating in the study, each child had a separate
bedroom, so a separate dust sample was collected. However,
all
analyses performed on only one child per home (177 children)
gave corresponding results, with even stronger significance
(data not shown).
In contrast to the results of the Swedish
DBH study (Bornehag et al. 2005a), we found no correlation
between concentrations of DEHP and BBzP in dust and the
presence of balatum in children's sleeping rooms.
One explanation can be that in Bulgaria the word balatum has
two meanings: linoleum or PVC. The fact that some of the "plastic" flooring
was in fact linoleum can therefore have weakened or even removed
any possible
correlation between PVC flooring and phthalate concentration.
For both studies, however, an association between health and
the
presence of PVC/balatum flooring in the child's
room was observed. In the present study, of 60 homes with balatum flooring
(34% of investigated homes), 41 were found in the homes of case
children (Table 1).
Because the use of polishing
agents and the concentration of phthalates are correlated with
each other and
both of them were associated with symptoms, the association
between health outcomes and DEHP concentration was tested in
both adjusted and stratified analyses. We found a
dose–response relationship between DEHP in dust and
symptoms both in buildings with high and low polish use, with
ORs in the highest quartiles (compared with the lowest quartile
group): OR = 4.20 (95% CI, 0.96–18.33) for case status,
and OR = 3.73 (95% CI, 0.85–16.44) for wheezing in the
group of homes with high polish use; and OR = 1.93 (95% CI,
0.62–5.98) for case status and OR = 2.67 (95% CI,
0.79–8.95) for wheezing in the low polish use group. Also,
with adjusting for polish use, the significant association
between the concentration of DEHP and case status/wheezing were
found for the highest quartile (compared with the lowest
quartile group): OR = 2.61 (95% CI, 1.07–6.37)
for case status, and OR = 3.08
(95% CI, 1.21–7.83) for wheezing in preceding
12 months. This means that the association between phthalates
and health cannot be explained by different use of polishing
agents only; however, the use of such compounds seems to
reinforce the association between health and the concentration
of selected phthalates.
It is reasonable to
expect that case families with asthma and allergy clean more
frequently than
control families, which could increase the amount and age of
the indoor dust and thus the content of phthalates in control
homes. In this study we found no difference in cleaning
frequency in homes of cases and controls, and we found the
opposite in dusting furniture—namely, that controls clean
more frequently than case families. Parents of 44% of controls
and 32% of cases reported that they customarily clean their
furniture more often than once a week. However, adjusting for
dusting frequency did not change the results in this study.
Additionally, the only phthalate significantly associated with
low dusting frequency was BBzP, which was found in
significantly higher concentrations in homes where dusting was
carried out once a week or less often, compared with more
frequent dusting (p = 0.007). DEHP and DnOP were
also found in higher concentrations in homes where dusting was
not as
frequent, compared with homes with more frequent dusting,
although this difference was not significant.
Compared with Sweden, there
were numerous problems in conducting the study in Bulgaria. The
response rate
in the cross-sectional study was very low (34.5%) compared with
Sweden (almost 80%). In the current case–control study,
several families refused to allow inspections or dust sampling,
despite having given prior consent. These differences are most
probably attributed to political and socioeconomic factors that
are outside the scope of this study.
A low response rate is always a problem in
epidemiologic investigations. However, such problems mainly
involve representativity and may not introduce bias when
analyzing associations between exposures and health effects.
The baseline study was used mainly to select possible cases
and
controls (sick and healthy children).
Because it is known that families with
allergic diseases are more prone to participate in
epidemiologic studies, potential selection bias in the baseline
questionnaire was investigated. A total of 240 children (78
in
Burgas and 162 in Sofia) were randomly selected among
nonresponders; they were contacted by phone and asked to answer
all questions used in the questionnaire. Excluding eczema in
preceding 12 months and asthma/allergic symptoms among family
members, there was no difference between the children whose
parents took part in the ALLHOME-1 study and those whose
parents refused to do so, limiting the risk for serious
selection bias regarding allergic and asthmatic symptoms and
diagnoses (Naydenov 2007).
Among children whose parents agreed to
participate in the ALLHOME-2 study, the prevalence of current
wheezing, rhinitis, and eczema was higher compared with
children whose parents did not agree to participate in the
ALLHOME-2 study or did not reply in the follow-up study
(Naydenov 2007). More health problems in the case families was
one of the selection factors for participation in the Swedish
DBH study (Bornehag et al. 2006). However, such selection bias
results in a greater contrast in health status between cases
and controls, and hence a greater possibility of identifying
differences in health-relevant exposures (Bornehag et al.
2006).
In this study, we
analyzed associations between children's health (as reported by parents), and
measured or inspected indoor environmental factors. A bias in
the baseline study could be introduced if parents with sick
children knew the risk factors for their child's illness
and reported more of such factors. However, such risk factors
were measured or observed by "blinded" inspectors
in the second phase. Also, the main potential risk factor
studied—the concentration of specific phthalates—is
not known to be a risk factor by the general public in
Bulgaria, Sweden, or elsewhere. A strong source of such
compounds, PVC flooring, could be recognized and reported, and
thus be a proxy for phthalates. This was not possible in
Bulgaria, where there is not even a word for PVC flooring,
because balatum is used for both PVC and linoleum
flooring. The same discussion is valid with regard to use of
polish.
This study and the DBH study in Sweden both
show an association between DEHP in indoor dust and airway
symptoms in preschool children. The two studies were performed
in very different regions of Europe with regard to building
type, climate, and political and socioeconomic factors. The
mechanisms behind these results are not known. Some toxicologic
studies have indicated that DEHP may act as an adjuvant factor
(Chalubinski and Kowalski 2006; Nielsen et al. 2007). However,
it is impossible to determine whether the important exposure
is
during childhood or during pregnancy.
The main finding of this study is that
phthalates in indoor dust could be found in all samples from
Bulgarian homes. The second main finding is that there is
a
significant association between the concentration of DEHP in
indoor dust and wheezing among preschool children.
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References
Adibi JJ, Perera FP, Jedrychowski
W, Camann DE, Barr D, Jacek R, et al. 2003. Prenatal exposures
to
phthalates among women in New York City and Krakow, Poland.
Environ Health Perspect 111:1719–1722.
Asher MI, Montefort S,
Bjorksten B, Lai ChKW, Strachan DP, Weiland SK, et al. 2006.
Worldwide time
trends in the prevalence of symptoms of asthma, allergic
rhinoconjunctivitis, and eczema in childhood: ISAAC Phase One
and three repeat multicountry cross-sectional surveys. Lancet
368:733–743.
Becker K, Seiwert M, Angerer
J, Heger W, Koch HM, Nagorka R, et al. 2004. DEHP metabolites
in urine of
children and DEHP in house dust. Int J Hyg Environ Health 207:
409–417.
Blount BC, Silva MJ, Caudill
SP, Needham LL, Pirkle JL, Sampson EJ, et al. 2000. Levels of
seven urinary
phthalate metabolites in a human reference population. Environ
Health Perspect 108:979–982.
Bornehag CG, Lundgren B,
Weschler ChJ, Sigsgaard T, Hägerhed-Engman L, Sundell J. 2005a.
Phthalates in indoor dust and their association with building
characteristics. Environ Health Perspect 113:1399–1404.
Bornehag CG, Sundell J,
Hagerhed-Engman L, Sigsgaard T, Janson S, Aberg N, DBH-study
group. 2005b. "Dampness" at home and its association with airway,
nose and skin symptoms among 10,851 preschool children in
Sweden: a cross sectional study. Indoor Air 15(suppl 10):
48–55.
Bornehag CG, Sundell J,
Sigsgaard T, Janson S. 2006. Potential self-selection bias in
a nested case
control study on indoor environmental factors and their
association with asthma and allergic symptoms among pre-school
children. Scand J Public Health 34:534–543.
Bornehag CG, Sundell J,
Weschler CJ, Sigsgaard T, Lundgren B, Hasselgren M, et al. 2004. The
association between asthma and allergic symptoms in children
and phthalates in house dust: a nested case–control
study. Environ Health Perspect 112:1393–1397.
Brasche S, Bischof W. 2005.
Daily time spent indoors in German homes-baseline data for the
assessment
of indoor exposure of German occupants. Int J Hyg Environ
Health 208(4):247–253.
Butte W, Hoffmann W, Hostrup
O, Schmidt A, Walker G. 2001. Endocrine disrupting chemicals
in house dust:
results of a representative monitoring. Gefahrstoffe
Reinhaltung Der Luft 61:19–23.
Calafat AM, Needham LL,
Silva MJ, Lambert G. 2004. Exposure to di-(2-ethylhexyl) phthalate
among
premature neonates in a neonatal intensive care unit.
Pediatrics 113:429–434.
Chalubinski M, Kowalski
ML. 2006. Endocrine disrupters—potential modulators of the immune
system and allergic response. Allergy 61:1326–1335.
Clausen PA, Bille RL, Nilsson
T, Hansen V, Svensmark B, Bøwadt S. 2003. Simultaneous extraction of
di(2-ethylhexyl) phthalate and non-ionic surfactants from house
dust. Concentrations in floor dust from 15 Danish schools. J
Chemogr A 986:179–190.
Fromme H, Lahrz T, Piloty
M, Gebhart H, Oddoy A, Ruden H. 2004. Occurrence of phthalates
and musk
fragrances in indoor air and dust from apartments and
kindergartens in Berlin (Germany). Indoor Air 14:188–195.
Glue C, Platzer MH, Larsen
ST, Nielsen GD, Skov PS, Poulsen LK. 2005. Phthalates potentiate the
response of allergic effector cells. Basic Clin Pharmacol
Toxicol 96:140–142.
Green R, Hauser R, Calafat
AM, Weuve J, Schettler T, Ringer S, et al. 2005. Use of di(2-ethylhexyl)
phthalate–containing medical products and urinary levels
of mono(2-ethylhexyl) phthalate in neonatal intensive care unit
infants. Environ Health Perspect 113:1222–1225.
ISAAC (International Study of Asthma and
Allergy in Childhood). 1998. ISAAC Phase Two. Available: http://isaac.auckland.ac.nz/Phasetwo/Phs2Frame.html [accessed 1 July
2007].
ISAAC Steering Committee.
1998. Worldwide variations in the prevalence of asthma symptoms:
the
International Study of Asthma and Allergies in Childhood
(ISAAC). Eur Respir J 12:315–335.
Jaakkola JJ, Ieromnimon
A, Jaakkola MS. 2006. Interior surface materials and asthma in
adults: a
population-based incident case-control study. Am J Epidemiol
164:742–749.
Jaakkola JJ, Øie L, Nafstad P,
Botten G, Samuelsen SO, Magnus P. 1999. Interior surface
materials in the home and the development of bronchial
obstruction in young children in Oslo, Norway. Am J Public
Health 89:188–192.
Jaakkola JJ, Verkasalo
PK, Jaakkola N. 2000. Plastic wall materials in the home and
respiratory health
in young children. Am J Public Health 90:797–799.
Kersten W, Reich T. 2003.
Schwerfluchtige organische umweltchemikalien in Hamburger hausstäben [in
German]. Reinhaltung der luft 63:85–91.
Koch HM, Drexler H, Angerer
J. 2003. An estimation of the daily intake of di(2-ethylhexyl)
phthalate
(DEHP) and other phthalates in the general population. Int J
Hyg Environ Health 206:77–83.
Koch HM, Preuss R, Drexler H, Angerer J.
2005. Exposure of nursery school children and their parents and
teachers to di-n-butylphthalate and butylbenzylphthalate. Int
Arch Occup Environ Health 78:223–229.
Larsen ST, Hansen J, Hansen
E, Clausen PA, Nielsen G. 2007. Airway inflammation and adjuvant
effects after
repeated airborne exposures to di-(2-ethylhexyl) phthalate and
ovalbumin in BALB/c mice. Toxicology 235:119–129.
Lee MH, Park J, Chung SW, Kang BY, Kim SH,
Kim TS. 2004. Enhancement of interleukin-4 production in
activated CD4+ T cells by diphthalate plasticizers
via increased NF-AT binding activity. Int Arch Allergy Immunol
134:
213–222.
Naydenov K. 2007. Association between Home
Exposure and Asthma and Allergies among Children in Bulgaria:
the ALLHOME study [PhD Thesis]. Lyngby:Technical University
of
Denmark.
Naydenov K, Sundell J,
Melikov A, Popov T, Bornehag CG, Stankov P, ALLHOME Project Group.
2005. The home
environment and allergies among Bulgarian children. In:
Proceedings of the Conference on Indoor Air Quality and Climate:
Indoor Air 2005, Beijing, China:Tsingua University Press,
3574–3575.
Nielsen G, Larsen ST, Olsen
O, Lovik M, Poulsen LK, Glue C, Wolkoff P. 2007. Do indoor chemicals
promote development of airway allergy? Indoor Air 17:
236–255.
Øie L, Hersoug LG, Madsen
JØ. 1997. Residential exposure to plasticizers and its
possible role in the pathogenesis of asthma. Environ Health
Perspect 105:972–978.
Platts-Mills TA, Erwin
E, Heymann P, Woodfolk J. 2005. Is the hygiene hypothesis still
a viable
explanation for the increased prevalence of asthma? Allergy
60(79):25–31.
Pohner A, Simrock S, Thumulla
J, Weber S, Wirkner T. 1997. Hintergrundbelastung des hausstaubes
von
privathauhalten mit mittel- und schwerfluchtigen organischen
schadstoffen [in German]. Umwelt Gesundheit 2:1–64.
Rudel RA, Camann DE, Spengler
JD, Korn LR, Brody JG. 2003. Phthalates, alkylophenols, pesticides,
polybrominated diphenyl ethers, and other endocrine-disturbing
compounds in indoor air and dust. Environ Sci Technol 37:
4543–4553.
Strachan DP. 1989. Hay
fever, hygiene and household size. BMJ 299:1259–1260.
World Health Organization. 2003. Children
at Risk! Main health Effects of Exposure to Environmental Risk
Factors. Fact Sheet EURO/05/03. Geneva:World Health
Organization Available: http://www.euro.who.int/document/mediacentre/fs0503e.pdf [accessed
7 November 2004].
Wormuth M, Scheringer M,
Vollenweider M, Hungerbuhler K. 2006. What are the sources of
exposure to eight
frequently used phthalic acid esters in Europeans? Risk Anal
26:
803–820. |
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