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- Choi, Hyunok, et al.
(författare)
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Common household chemicals and the allergy risks in pre-school age children
- 2010
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Ingår i: PLOS ONE. - : Public Library of Science. - 1932-6203. ; 5:10
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Tidskriftsartikel (refereegranskat)abstract
- BACKGROUND: The risk of indoor exposure to volatile organic compounds (VOCs) on allergic airway diseases in children remains unknown.OBJECTIVE: We examined the residential concentrations of VOCs, emitted from building materials, paints, furniture, and other lifestyle practices and the risks of multiple allergic diseases as well as the IgE-sensitization in pre-school age children in Sweden.METHODS: In a case-control investigation (198 case children with asthma and allergy and 202 healthy controls), air samples were collected in the room where the child slept. The air samples were analyzed for the levels of eight classes of VOCs.RESULTS: A natural-log unit of summed propylene glycol and glycol ethers (PGEs) in bedroom air (equal to interquartile range, or 3.43 - 15.65 µg/m(3)) was associated with 1.5-fold greater likelihood of being a case (95% CI, 1.1 - 2.1), 1.5-fold greater likelihood of asthma (95% CI, 1.0 - 2.3), 2.8-fold greater likelihood of rhinitis (95% CI, 1.6 - 4.7), and 1.6-fold greater likelihood of eczema (95% CI, 1.1 - 2.3), accounting for gender, secondhand smoke, allergies in both parents, wet cleaning with chemical agents, construction period of the building, limonene, cat and dog allergens, butyl benzyl phthalate (BBzP), and di(2-ethylhexyl)phthalate (DEHP). When the analysis was restricted to the cases, the same unit concentration was associated with 1.8-fold greater likelihood of IgE-sensitization (95% CI, 1.1 - 2.8) compared to the non-IgE sensitized cases. No similar associations were found for the other classes of VOCs.CONCLUSION: We propose a novel hypothesis that PGEs in indoor air exacerbate and/or induce the multiple allergic symptoms, asthma, rhinitis and eczema, as well as IgE sensitization respectively.
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- Choi, Hyunok, et al.
(författare)
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Non-microbial sources of microbial volatile organic compounds
- 2016
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Ingår i: Environmental Research. - : Academia Press. - 0013-9351 .- 1096-0953. ; 148, s. 127-136
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Tidskriftsartikel (refereegranskat)abstract
- Background: The question regarding the true sources of the purported microbial volatile organic compounds (MVOCs) remains unanswered. Objective: To identify microbial, as well as non-microbial sources of 28 compounds, which are commonly accepted as microbial VOCs (i.e. primary outcome of interest is σ 28 VOCs). Methods: In a cross-sectional investigation of 390 homes, six building inspectors assessed water/mold damage, took air and dust samples, and measured environmental conditions (i.e., absolute humidity (AH, g/m3), temperature (°C), ventilation rate (ACH)). The air sample was analyzed for volatile organic compounds (μg/m3) and; dust samples were analyzed for total viable fungal concentration (CFU/g) and six phthalates (mg/g dust). Four benchmark variables of the underlying sources were defined as highest quartile categories of: 1) the total concentration of 17 propylene glycol and propylene glycol ethers (σ17 PGEs) in the air sample; 2) 2,2,4-trimethyl-1,3-pentanediol monoisobutyrate (TMPD-MIB) in the air sample; 3) semi-quantitative mold index; and 4) total fungal load (CFU/g). Results: Within severely damp homes, co-occurrence of the highest quartile concentration of either σ17 PGEs or TMPD-MIB were respectively associated with a significantly higher median concentration of σ 28 VOCs (8.05 and 13.38 μg/m3, respectively) compared to the reference homes (4.30 and 4.86 μg/m3, respectively, both Ps ≤0.002). Furthermore, the homes within the highest quartile range for σ fungal load as well as AH were associated with a significantly increased median σ 28 VOCs compared to the reference group (8.74 vs. 4.32 μg/m3, P=0.001). Within the final model of multiple indoor sources on σ 28 VOCs, one natural log-unit increase in summed concentration of σ17 PGEs, plus TMPD-MIB (σ 17 PGEs + TMPD-MIB) was associated with 1.8-times (95% CI, 1.3-2.5), greater likelihood of having a highest quartile of σ 28 VOCs, after adjusting for absolute humidity, history of repainting at least one room, ventilation rate, and mold index (P-value =0.001). Homes deemed severely mold damaged (i.e., mold index =1) were associated with 1.7-times (95% CI, 0.8-3.6), greater likelihood of having a highest quartile of σ 28 VOCs, even though such likelihood was not significant (P-value =0.164). In addition, absolute humidity appeared to positively interact with mold index to significantly elevate the prevalence of the highest quartile category of σ 28 VOCs. Conclusion: The indoor concentration of σ 28 VOCs, which are widely accepted as MVOCs, are significantly associated with the markers of synthetic (i.e. σ17 PGEs and TMPD-MIB), and to less extent, microbial (i.e., mold index) sources.
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| 4. |
- Choi, Hyunok, et al.
(författare)
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Volatile organic compounds of possible microbial origin and their risks on childhood asthma and allergies within damp homes
- 2017
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Ingår i: Environment International. - : Elsevier BV. - 0160-4120 .- 1873-6750. ; 98, s. 143-151
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Tidskriftsartikel (refereegranskat)abstract
- Background Risk of indoor exposure to volatile organic compounds of purported microbial origin on childhood symptoms of wheezing, rhinitis, and/or eczema, and doctor-diagnosed asthma, rhinitis, and eczema, respectively, remain unclear. Objective To test hypotheses that total sum of 28 microbial volatile organic compounds (Σ26 MVOCs): 1) poses independent risk on doctor-diagnosed asthma, rhinitis, and eczema, respectively, as well as multiple symptom presentation with a minimum of the two of the above conditions (i.e. case); 2) is associated with significant interaction with absolute humidity (AH) on additive scale. Methods In a case-control investigation, 198 cases and 202 controls were examined during November 2001 – March 2002 period through home indoor air sampling, air quality inspection, and health outcome ascertainment. Results Not only the Σ28 MVOCs but also the global MVOC index were significantly higher within the homes of the cases with a high AH, compared to the controls with a low AH (all Ps < 0.001). Only the cases, but not the controls, were associated with a dose-dependent increase in the exposure variables of interest (Σ28 MVOCs) per quartile increase in AH (P < 0.0001 for the cases; P = 0.780 for the controls). Only among the children who live in a high AH homes, a natural log (ln)-unit of Σ 28 MVOCs was associated with 2.5-times greater odds of the case status (95% CI, 1.0–6.2; P = 0.046), compared to 0.7-times the odds (95% CI, 0.4–1.0; P = 0.074) of the same outcome among the low AH homes. Specifically, joint exposure to a high MVOCs and high AH was associated with 2.6-times greater odds of the doctor-diagnosed asthma status (95% CI, 0.7–8.91; P = 0.137). Conclusion Joint occurrence of high Σ28 MVOCs and AH was associated with a significant increase in the case status and asthma risks in an additive scale.
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- Eneroth, Kristina, et al.
(författare)
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Springtime depletion of tropospheric ozone, gaseous elemental mercury and non-methane hydrocarbons in the European Arctic, and its relation to atmospheric transport
- 2007
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Ingår i: Atmospheric Environment. - : Elsevier BV. - 1352-2310 .- 1873-2844. ; 41:38, s. 8511-8526
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Tidskriftsartikel (refereegranskat)abstract
- Using a trajectory climatology for the period 1992-2001 we have examined how seasonal changes in transport cause changes in the concentrations of tropospheric ozone (O-3), gaseous elemental mercury (GEM) and non-methane hydrocarbons (NMHCs) observed at the Mt. Zeppelin station, Ny-angstrom lesund (78.9 degrees N, 11.9 degrees E). During April-June O-3 depletion events were frequently observed in connection with air transport across the Arctic Basin. The O-3 loss was most pronounced in air masses advected close to the surface. This result supports the idea that the O-3 depletion reactions take place in the lowermost part of the atmosphere in the central Arctic Basin. A strong positive correlation between springtime O-3 depletion events and the oxidation of GEM to divalent mercury was found. During air mass advection from Siberia, the Barents Sea and the Norwegian Sea the strongest correlation was observed during April-May, whereas air masses originating from the Canadian Arctic and the central Arctic areas showed the highest O-3-GEM correlation in May-June. We suggest that this 1-month lag could either be due to the position of the marginal ice zone or temperature differences between the northwestern and northeastern air masses. In connection with springtime O-3 depletion events low concentrations of some NMHCs, especially ethane and ethyne, were observed, indicating that both bromine (ethyne oxidant) and chlorine radicals (ethane oxidant) are present in the Arctic atmosphere during spring. In winter, negative correlations between O-3 and NMHCs were found in connection with air transport from Europe and Siberia, which we interpret as O-3 destruction taking place in industrially contaminated plumes.
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| 6. |
- Platt, Stephen M., et al.
(författare)
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Atmospheric composition in the European Arctic and 30 years of the Zeppelin Observatory, Ny-Ålesund
- 2022
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Ingår i: Atmospheric Chemistry And Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 22:5, s. 3321-3369
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Tidskriftsartikel (refereegranskat)abstract
- The Zeppelin Observatory (78.90∘ N, 11.88∘ E) is located on Zeppelin Mountain at 472 m a.s.l. on Spitsbergen, the largest island of the Svalbard archipelago. Established in 1989, the observatory is part of Ny-Ålesund Research Station and an important atmospheric measurement site, one of only a few in the high Arctic, and a part of several European and global monitoring programmes and research infrastructures, notably the European Monitoring and Evaluation Programme (EMEP); the Arctic Monitoring and Assessment Programme (AMAP); the Global Atmosphere Watch (GAW); the Aerosol, Clouds and Trace Gases Research Infrastructure (ACTRIS); the Advanced Global Atmospheric Gases Experiment (AGAGE) network; and the Integrated Carbon Observation System (ICOS). The observatory is jointly operated by the Norwegian Polar Institute (NPI), Stockholm University, and the Norwegian Institute for Air Research (NILU). Here we detail the establishment of the Zeppelin Observatory including historical measurements of atmospheric composition in the European Arctic leading to its construction. We present a history of the measurements at the observatory and review the current state of the European Arctic atmosphere, including results from trends in greenhouse gases, chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs), other traces gases, persistent organic pollutants (POPs) and heavy metals, aerosols and Arctic haze, and atmospheric transport phenomena, and provide an outline of future research directions.
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