-
Je něco špatně v tomto záznamu ?
Greater susceptibility of girls to airborne Benzo[a]pyrene for obesity-associated childhood asthma
H. Choi, M. Dostal, A. Pastorkova, P. Rossner, RJ. Sram, SM. Ho,
Jazyk angličtina Země Nizozemsko
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
- MeSH
- benzopyren toxicita MeSH
- bronchiální astma chemicky indukované etiologie MeSH
- dítě MeSH
- látky znečišťující vzduch toxicita MeSH
- lidé MeSH
- logistické modely MeSH
- mladiství MeSH
- obezita dětí a dospívajících komplikace MeSH
- pohlavní dimorfismus * MeSH
- pohlavní dospělost MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
BACKGROUND: Sexually dimorphic risk of obesity-associated asthma is posited to accelerate around puberty. Yet, the role of air pollution on the lean and obese asthmatic children has never been examined. OBJECTIVE: To compare whether a unit exposure to airborne benzo[a]pyrene (B[a]P) is associated with altered risks of asthma across the overweight/obese (OV/OB) control, lean asthmatic, and OV/OB asthmatic children, respectively, compared to the lean controls, before and after adjusting for oxidant stress markers (i.e. 15‐F2t‐IsoP, 8‐oxo‐dG, and Carbonyl). METHODS: Asthmatic and healthy control children, recruited from polluted urban and rural areas, were matched to ambient concentration of B[a]P. A unit increase in B[a]P and multinomial logistic regression on OV/OB control, lean asthmatic, and OV/OB asthma were compared across the sex- and age-groups. RESULTS: The median B[a]P was associated with a linear increase among the female children, according to OV/OB and asthma, respectively, and together, compared to the lean control girls (p = 0.001). While B[a]P was associated with positive relationship with 15‐F2t‐IsoP level among the OV/OB boys, the same exposure-outcome association was inverse among the OV/OB girls. One natural log-unit increase in ambient B[a]P was associated with 10.5-times greater odds (95% CI, 2.6-39.6; p = 0.001) the adolescent OV/OB boys, compared to the unit odds among the lean controls. In contrast, the adolescent OV/OB girls were associated with highest adjusted odds of the asthma (aOR = 15.4; 95% CI, 2.9-29.1; p < 0.001) compared to the lean control girls. An adjustment for 15‐F2t‐IsoP, and Carbonyls was associated with greater odds of asthma per unit exposure for the adolescent OV/OB girls (aOR = 16.2; 95% CI, 1.4-181.8; p = 0.024). CONCLUSIONS: B[a]P exposure was associated with a leap in the odds of asthma among the OV/OB adolescents, particularly the girls, after adjusting for 15‐F2t‐IsoP and Carbonyls.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19028197
- 003
- CZ-PrNML
- 005
- 20240620092518.0
- 007
- ta
- 008
- 190813s2018 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.envint.2018.08.061 $2 doi
- 035 __
- $a (PubMed)30237028
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Choi, Hyunok $u Departments of Environmental Health Sciences, Epidemiology, and Biostatistics, University at Albany School of Public Health One University Place, Rm 153, Rensselaer, NY 12144-3456, USA. Electronic address: hchoi@albany.edu.
- 245 10
- $a Greater susceptibility of girls to airborne Benzo[a]pyrene for obesity-associated childhood asthma / $c H. Choi, M. Dostal, A. Pastorkova, P. Rossner, RJ. Sram, SM. Ho,
- 520 9_
- $a BACKGROUND: Sexually dimorphic risk of obesity-associated asthma is posited to accelerate around puberty. Yet, the role of air pollution on the lean and obese asthmatic children has never been examined. OBJECTIVE: To compare whether a unit exposure to airborne benzo[a]pyrene (B[a]P) is associated with altered risks of asthma across the overweight/obese (OV/OB) control, lean asthmatic, and OV/OB asthmatic children, respectively, compared to the lean controls, before and after adjusting for oxidant stress markers (i.e. 15‐F2t‐IsoP, 8‐oxo‐dG, and Carbonyl). METHODS: Asthmatic and healthy control children, recruited from polluted urban and rural areas, were matched to ambient concentration of B[a]P. A unit increase in B[a]P and multinomial logistic regression on OV/OB control, lean asthmatic, and OV/OB asthma were compared across the sex- and age-groups. RESULTS: The median B[a]P was associated with a linear increase among the female children, according to OV/OB and asthma, respectively, and together, compared to the lean control girls (p = 0.001). While B[a]P was associated with positive relationship with 15‐F2t‐IsoP level among the OV/OB boys, the same exposure-outcome association was inverse among the OV/OB girls. One natural log-unit increase in ambient B[a]P was associated with 10.5-times greater odds (95% CI, 2.6-39.6; p = 0.001) the adolescent OV/OB boys, compared to the unit odds among the lean controls. In contrast, the adolescent OV/OB girls were associated with highest adjusted odds of the asthma (aOR = 15.4; 95% CI, 2.9-29.1; p < 0.001) compared to the lean control girls. An adjustment for 15‐F2t‐IsoP, and Carbonyls was associated with greater odds of asthma per unit exposure for the adolescent OV/OB girls (aOR = 16.2; 95% CI, 1.4-181.8; p = 0.024). CONCLUSIONS: B[a]P exposure was associated with a leap in the odds of asthma among the OV/OB adolescents, particularly the girls, after adjusting for 15‐F2t‐IsoP and Carbonyls.
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a látky znečišťující vzduch $x toxicita $7 D000393
- 650 _2
- $a bronchiální astma $x chemicky indukované $x etiologie $7 D001249
- 650 _2
- $a benzopyren $x toxicita $7 D001564
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a logistické modely $7 D016015
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a obezita dětí a dospívajících $x komplikace $7 D063766
- 650 12
- $a pohlavní dimorfismus $7 D012727
- 650 _2
- $a pohlavní dospělost $7 D012741
- 655 _2
- $a srovnávací studie $7 D003160
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Dostál, Miroslav, $d 1941- $u Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, 142 20 Prague 4, Czech Republic. $7 xx0075980
- 700 1_
- $a Pastorkova, Anna $u Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, 142 20 Prague 4, Czech Republic.
- 700 1_
- $a Rossner, Pavel $u Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, 142 20 Prague 4, Czech Republic. Electronic address: prossner@biomed.cas.cz.
- 700 1_
- $a Sram, Radim J $u Department of Genetic Toxicology and Nanotoxicology, Institute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, 142 20 Prague 4, Czech Republic. Electronic address: sram@biomed.cas.cz.
- 700 1_
- $a Ho, Shuk-Mei $u Department of Environmental Health, University of Cincinnati, Cincinnati, OH, USA. Electronic address: hosm@ucmail.uc.edu.
- 773 0_
- $w MED00001541 $t Environment international $x 1873-6750 $g Roč. 121, č. Pt 1 (2018), s. 308-316
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30237028 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20240620092519 $b ABA008
- 999 __
- $a ok $b bmc $g 1433346 $s 1066657
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2018 $b 121 $c Pt 1 $d 308-316 $e 20180917 $i 1873-6750 $m Environment international $n Environ Int $x MED00001541
- LZP __
- $a Pubmed-20190813