» Articles » PMID: 37020834

Plasma Sphingolipids, Lung Function and COPD: the Cardiovascular Health Study

Overview
Journal ERJ Open Res
Specialty Pulmonary Medicine
Date 2023 Apr 6
PMID 37020834
Authors
Affiliations
Soon will be listed here.
Abstract

Rationale: COPD is the third leading cause of death in the United States. Sphingolipids, structural membrane constituents that play a role in cellular stress and apoptosis signalling, may be involved in lung function.

Methods: In the Cardiovascular Health Study, a prospective cohort of older adults, we cross-sectionally examined the association of plasma levels of 17 sphingolipid species with lung function and COPD. Multivariable linear regression and logistic regression were used to evaluate associations of sphingolipid concentrations with forced expiratory volume in 1 s (FEV) and odds of COPD, respectively.

Results: Of the 17 sphingolipids evaluated, ceramide-18 (Cer-18) and sphingomyelin-18 (SM-18) were associated with lower FEV values (-0.061 L per two-fold higher Cer-18, p=0.001; -0.092 L per two-fold higher SM-18, p=0.002) after correction for multiple testing. Several other associations were significant at a 0.05 level, but did not reach statistical significance after correction for multiple testing. Specifically, Cer-18 and SM-18 were associated with higher odds of COPD (odds ratio per two-fold higher Cer-18 1.29, p=0.03 and SM-18 1.73, p=0.008). Additionally, Cer-16 and SM-16 were associated with lower FEV values, and Cer-14, SM-14 and SM-16 with a higher odds of COPD.

Conclusion: In this large cross-sectional study, specific ceramides and sphingomyelins were associated with reduced lung function in a population-based study. Future studies are needed to examine whether these biomarkers are associated with longitudinal change in FEV within individuals or with incident COPD.

References
1.
Levy M, Khan E, Careaga M, Goldkorn T . Neutral sphingomyelinase 2 is activated by cigarette smoke to augment ceramide-induced apoptosis in lung cell death. Am J Physiol Lung Cell Mol Physiol. 2009; 297(1):L125-33. PMC: 2711801. DOI: 10.1152/ajplung.00031.2009. View

2.
Turpin-Nolan S, Bruning J . The role of ceramides in metabolic disorders: when size and localization matters. Nat Rev Endocrinol. 2020; 16(4):224-233. DOI: 10.1038/s41574-020-0320-5. View

3.
Chakinala R, Khatri A, Gupta K, Koike K, Epelbaum O . Sphingolipids in COPD. Eur Respir Rev. 2019; 28(154). PMC: 9488540. DOI: 10.1183/16000617.0047-2019. View

4.
Bowler R, Jacobson S, Cruickshank C, Hughes G, Siska C, Ory D . Plasma sphingolipids associated with chronic obstructive pulmonary disease phenotypes. Am J Respir Crit Care Med. 2014; 191(3):275-84. PMC: 4351578. DOI: 10.1164/rccm.201410-1771OC. View

5.
Petrache I, Kamocki K, Poirier C, Pewzner-Jung Y, Laviad E, Schweitzer K . Ceramide synthases expression and role of ceramide synthase-2 in the lung: insight from human lung cells and mouse models. PLoS One. 2013; 8(5):e62968. PMC: 3653891. DOI: 10.1371/journal.pone.0062968. View