Effect of Variation in CHI3L1 on Serum YKL-40 Level, Risk of Asthma, and Lung Function

The chitinase-like protein YKL-40 is known to be involved in inflammation and tissue remodeling and is a biomarker of asthma severity and pulmonary function. This study shows an association between markers in the gene encoding YKL-40 and asthma, indicating that YKL-40 levels not only serve as a biom...

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Veröffentlicht in:The New England journal of medicine 2008-04, Vol.358 (16), p.1682-1691
Hauptverfasser: Ober, Carole, Tan, Zheng, Sun, Ying, Possick, Jennifer D, Pan, Lin, Nicolae, Raluca, Nicolae, Dan L, Radford, Sadie, Parry, Rodney R, Heinzmann, Andrea, Deichmann, Klaus A, Lester, Lucille A, Gern, James E, Lemanske, Robert F, Elias, Jack A, Chupp, Geoffrey L
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Sprache:eng
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Zusammenfassung:The chitinase-like protein YKL-40 is known to be involved in inflammation and tissue remodeling and is a biomarker of asthma severity and pulmonary function. This study shows an association between markers in the gene encoding YKL-40 and asthma, indicating that YKL-40 levels not only serve as a biomarker but also contribute to disease susceptibility. This study shows an association between markers in the gene encoding YKL-40 and asthma, indicating that YKL-40 levels not only serve as a biomarker but also contribute to disease susceptibility. Chitinases are evolutionarily conserved proteins that mediate airway inflammation in mouse models of asthma. 1 The chitinase-like protein YKL-40 lacks chitinase activity but binds ubiquitously expressed chitin and has been implicated in inflammation and tissue remodeling. 2 – 6 We recently demonstrated that serum YKL-40 levels are elevated in patients with asthma and that circulating YKL-40 levels are correlated with asthma severity, thickness of the subepithelial basement membrane, and pulmonary function, 7 suggesting that circulating YKL-40 levels are a biomarker for asthma. The YKL-40 protein is encoded by the chitinase 3–like 1 gene CHI3L1, and single-nucleotide polymorphisms (SNPs) in the CHI3L1 promoter have been . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa0708801