Title | Adhesion molecules, endothelin-1 and lung function in seven population-based cohorts. |
Publication Type | Journal Article |
Year of Publication | 2013 |
Authors | Oelsner, EC, Pottinger, TD, Burkart, KM, Allison, M, Buxbaum, SG, Hansel, NN, Kumar, R, Larkin, EK, Lange, LA, Loehr, LR, London, SJ, O'Connor, GT, Papanicolaou, G, Petrini, MF, Rabinowitz, D, Raghavan, S, Redline, S, Thyagarajan, B, Tracy, RP, Wilk, JB, White, WB, Rich, SS, Barr, RG |
Journal | Biomarkers |
Volume | 18 |
Issue | 3 |
Pagination | 196-203 |
Date Published | 2013 May |
ISSN | 1366-5804 |
Other Numbers | Collaborator |
Keywords | African Continental Ancestry Group, Biomarkers, Cohort Studies, E-Selectin, Endothelin-1, Endothelium, Vascular, European Continental Ancestry Group, Female, Gene Expression, Humans, Intercellular Adhesion Molecule-1, Lung, Male, Middle Aged, P-Selectin, Pulmonary Disease, Chronic Obstructive, Respiratory Function Tests, Spirometry |
Abstract | <p><b>CONTEXT: </b>Endothelial function is abnormal in chronic obstructive pulmonary disease (COPD); whether endothelial dysfunction causes COPD is unknown.</p><p><b>OBJECTIVE: </b>Test associations of endothelial biomarkers with FEV1 using instrumental variables.</p><p><b>METHODS: </b>Among 26 907 participants with spirometry, ICAM-1, P-selectin, E-selectin and endothelin-1 were measured in subsets.</p><p><b>RESULTS: </b>ICAM-1 and P-selectin were inversely associated with FEV1 among European-Americans (-29 mL and -34 mL per standard deviation of log-transformed biomarker, p < 0.001), as was endothelin-1 among African-Americans (-22 mL, p = 0.008). Genetically-estimated ICAM-1 and P-selectin were not significantly associated with FEV1. The instrumental variable for endothelin-1 was non-informative.</p><p><b>CONCLUSION: </b>Although ICAM-1, P-selectin and endothelin-1 were inversely associated with FEV1, associations for ICAM-1 and P-selectin do not appear causal.</p> |
DOI | 10.3109/1354750X.2012.762805 |
Alternate Journal | Biomarkers |
PubMed ID | 23557128 |
PubMed Central ID | PMC3890095 |
Grant List | UL1RR025005 / RR / NCRR NIH HHS / United States N01-HC-25195 / HC / NHLBI NIH HHS / United States R01-HL-077612 / HL / NHLBI NIH HHS / United States HL-096917 / HL / NHLBI NIH HHS / United States HHSN268201100009I / HL / NHLBI NIH HHS / United States N01-HC-45205 / HC / NHLBI NIH HHS / United States N01-HC-95162 / HC / NHLBI NIH HHS / United States R01-HL-086694 / HL / NHLBI NIH HHS / United States U01 HL096812 / HL / NHLBI NIH HHS / United States N01-HC-05187 / HC / NHLBI NIH HHS / United States N01HC95160 / HL / NHLBI NIH HHS / United States R01 HL071251 / HL / NHLBI NIH HHS / United States R01 HL046380 / HL / NHLBI NIH HHS / United States R01 HL053560 / HL / NHLBI NIH HHS / United States R01-HL-071258 / HL / NHLBI NIH HHS / United States HHSN268201100010C / HL / NHLBI NIH HHS / United States R01 HL071259 / HL / NHLBI NIH HHS / United States R01 AG015928 / AG / NIA NIH HHS / United States N01HC95163 / HL / NHLBI NIH HHS / United States U01 HL080295 / HL / NHLBI NIH HHS / United States N01-HC-48047 / HC / NHLBI NIH HHS / United States HHSN268201100005G / HL / NHLBI NIH HHS / United States R01 HL071252 / HL / NHLBI NIH HHS / United States N01HC48049 / HL / NHLBI NIH HHS / United States U01 HL096917 / HL / NHLBI NIH HHS / United States N01-HC-85081 / HC / NHLBI NIH HHS / United States HHSN268201100005C / / PHS HHS / United States N01HC45205 / HL / NHLBI NIH HHS / United States R01 HL059367 / HL / NHLBI NIH HHS / United States HHSN268201100007C / HL / NHLBI NIH HHS / United States RR-024156 / RR / NCRR NIH HHS / United States R01-HL-087641 / HL / NHLBI NIH HHS / United States HHSN268200800007C / HL / NHLBI NIH HHS / United States N01-HC-95163 / HC / NHLBI NIH HHS / United States R01-HL-071250 / HL / NHLBI NIH HHS / United States N01 HC015103 / HC / NHLBI NIH HHS / United States N01-HC-95168 / HC / NHLBI NIH HHS / United States N01HC95169 / HL / NHLBI NIH HHS / United States R56 AG020098 / AG / NIA NIH HHS / United States R01 HL077612 / HL / NHLBI NIH HHS / 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