Cardiovascular disease-linked plasma proteins are mainly associated with lung volume. Issue 2 (27th March 2023)
- Record Type:
- Journal Article
- Title:
- Cardiovascular disease-linked plasma proteins are mainly associated with lung volume. Issue 2 (27th March 2023)
- Main Title:
- Cardiovascular disease-linked plasma proteins are mainly associated with lung volume
- Authors:
- Rydell, Andreas
Nerpin, Elisabet
Zhou, XingWu
Lind, Lars
Lindberg, Eva
Theorell Haglöw, Jenny
Fall, Tove
Janson, Christer
Lisspers, Karin
Elmståhl, Sölve
Zaigham, Suneela
Melander, Olle
Nilsson, Peter M.
Ärnlöv, Johan
Malinovschi, Andrei - Abstract:
- Background: Epidemiological studies have shown that impaired lung function is common and associated with increased risk of cardiovascular disease. Increased levels of several inflammatory and cardiovascular disease-related plasma proteins have been associated with impaired lung function. The aim was to study the association between plasma proteomics and forced expiratory volume in 1 s (FEV1 ), forced vital capacity (FVC) and FEV1 /FVC ratio. Methods: We used a discovery and replication approach in two community-based cohorts, EpiHealth and the Malmö Offspring Study (total n=2874), to cross-sectionally study 242 cardiovascular disease- and metabolism-linked proteins in relation to FEV1, FVC (both % predicted) and FEV1 /FVC ratio. A false discovery rate of 5% was used as the significance threshold in the discovery cohort. Results: Plasma fatty acid-binding protein 4, interleukin-1 receptor antagonist, interleukin-6 and leptin were negatively associated with FEV1 and paraoxonase 3 was positively associated therewith. Fatty acid-binding protein 4, fibroblast growth factor 21, interleukin-1 receptor antagonist, interleukin-6 and leptin were negatively associated with FVC and agouti-related protein, insulin-like growth factor-binding protein 2, paraoxonase 3 and receptor for advanced glycation end products were positively associated therewith. No proteins were associated with FEV1 /FVC ratio. A sensitivity analysis in EpiHealth revealed only minor changes after excludingBackground: Epidemiological studies have shown that impaired lung function is common and associated with increased risk of cardiovascular disease. Increased levels of several inflammatory and cardiovascular disease-related plasma proteins have been associated with impaired lung function. The aim was to study the association between plasma proteomics and forced expiratory volume in 1 s (FEV1 ), forced vital capacity (FVC) and FEV1 /FVC ratio. Methods: We used a discovery and replication approach in two community-based cohorts, EpiHealth and the Malmö Offspring Study (total n=2874), to cross-sectionally study 242 cardiovascular disease- and metabolism-linked proteins in relation to FEV1, FVC (both % predicted) and FEV1 /FVC ratio. A false discovery rate of 5% was used as the significance threshold in the discovery cohort. Results: Plasma fatty acid-binding protein 4, interleukin-1 receptor antagonist, interleukin-6 and leptin were negatively associated with FEV1 and paraoxonase 3 was positively associated therewith. Fatty acid-binding protein 4, fibroblast growth factor 21, interleukin-1 receptor antagonist, interleukin-6 and leptin were negatively associated with FVC and agouti-related protein, insulin-like growth factor-binding protein 2, paraoxonase 3 and receptor for advanced glycation end products were positively associated therewith. No proteins were associated with FEV1 /FVC ratio. A sensitivity analysis in EpiHealth revealed only minor changes after excluding individuals with known cardiovascular disease, diabetes or obesity. Conclusions: Five proteins were associated with both FEV1 and FVC. Four proteins associated with only FVC and none with FEV1 /FVC ratio, suggesting associations mainly through lung volume, not airway obstruction. However, additional studies are needed to investigate underlying mechanisms for these findings. Several cardiovascular disease-linked proteins were associated with FEV1 and FVC, but not with FEV1 /FVC ratio, suggesting that the relationships are mainly with lung volume, not airflow obstruction https://bit.ly/3j19Io8 … (more)
- Is Part Of:
- ERJ open research. Volume 9:Issue 2(2023)
- Journal:
- ERJ open research
- Issue:
- Volume 9:Issue 2(2023)
- Issue Display:
- Volume 9, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 9
- Issue:
- 2
- Issue Sort Value:
- 2023-0009-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-03-27
- Subjects:
- Respiratory organs -- Diseases -- Periodicals
Respiration -- Periodicals
Respiration
Respiratory organs -- Diseases
Respiratory organs -- Diseases -- Treatment
Respiratory Tract Diseases
Electronic journals
Fulltext
Internet Resources
Periodicals
Periodical
616.2005 - Journal URLs:
- http://openres.ersjournals.com/ ↗
http://bibpurl.oclc.org/web/76947 ↗ - DOI:
- 10.1183/23120541.00321-2022 ↗
- Languages:
- English
- ISSNs:
- 2312-0541
- Deposit Type:
- Legaldeposit
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- British Library HMNTS - ELD Digital store
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- 26748.xml