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Article

The inflammatory biomarker YKL-40 is elevated in the serum, but not the sputum, of E-cigarette users

ORCID Icon, , &
Pages 55-66 | Received 27 Mar 2020, Accepted 03 Nov 2020, Published online: 17 Nov 2020
 

Abstract

Rationale: E-cigarettes are popular among youth and young adults and have been shown to be associated with pulmonary conditions such as asthma and COPD. YKL-40 may serve as a biomarker of pulmonary diseases and may predict the loss of pulmonary function among smokers. We hypothesized that similar to cigarette smokers, e-cigarette users will have higher levels of YKL-40 compared to non-tobacco users.

Methods

We conducted a cross-sectional study of adults between 18 and 55 years old. Inclusion criteria were: exclusive e-cigarette use or cigarette smoking for ≥ 1 year or no history of tobacco use.

Participants with a history of pulmonary illness, atopy, medications (except birth control pills), marijuana, and illegal substance use were excluded. Custom Multiplex ELISA was used to measure YKL-40 and other biomarker levels in the serum and induced sputum of the participants. Multivariable linear regression was used to compare the levels of YLK-40 in healthy participants, e-cigarette, and cigarette users after adjusting for age, sex, and BMI.

Results

We recruited 20 healthy controls, 23 cigarette smokers, and 22 exclusive e-cigarette users. Serum YKL-40 (ng/ml) was significantly higher in e-cigarette users (Median 21.2 [IQR 12.1-24.0] ng/ml) when compared to controls (12.2 [IQR 8.7-18.1] ng/ml, p = 0.016) but comparable to cigarette smokers (21.6 [IQR 11.62-51.7] ng/ml, p = 0.31). No significant differences were found in the serum or sputum of the other biomarkers tested.

Conclusion

The inflammatory biomarker, YKL-40 is elevated in the serum but not the sputum of e-cigarette users with no reported pulmonary disease. Further research is necessary to characterize this association.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by National Cancer Institute, R01 CA207491; National Heart, Lung, and Blood Institute, PRIDE-AiRE.

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