Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis

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Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis. / Iversen, Line V; Ullman, Susanne; Østergaard, Ole; Nielsen, Christoffer T; Halberg, Poul; Karlsmark, Tonny; Heegaard, Niels H. H.; Jacobsen, Søren.

In: BMC Musculoskeletal Disorders, Vol. 16, 191, 2015.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Iversen, LV, Ullman, S, Østergaard, O, Nielsen, CT, Halberg, P, Karlsmark, T, Heegaard, NHH & Jacobsen, S 2015, 'Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis', BMC Musculoskeletal Disorders, vol. 16, 191. https://doi.org/10.1186/s12891-015-0653-8

APA

Iversen, L. V., Ullman, S., Østergaard, O., Nielsen, C. T., Halberg, P., Karlsmark, T., Heegaard, N. H. H., & Jacobsen, S. (2015). Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis. BMC Musculoskeletal Disorders, 16, [191]. https://doi.org/10.1186/s12891-015-0653-8

Vancouver

Iversen LV, Ullman S, Østergaard O, Nielsen CT, Halberg P, Karlsmark T et al. Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis. BMC Musculoskeletal Disorders. 2015;16. 191. https://doi.org/10.1186/s12891-015-0653-8

Author

Iversen, Line V ; Ullman, Susanne ; Østergaard, Ole ; Nielsen, Christoffer T ; Halberg, Poul ; Karlsmark, Tonny ; Heegaard, Niels H. H. ; Jacobsen, Søren. / Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis. In: BMC Musculoskeletal Disorders. 2015 ; Vol. 16.

Bibtex

@article{1e1a14e70f5f49c897663c338468a595,
title = "Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis",
abstract = "BACKGROUND: Endothelial damage and activation may play central roles in the pathogenesis of systemic sclerosis (SSc) and are reflected by microparticles (MPs) and soluble selectins. The objective of this study was to determine if these potential biomarkers are associated with specific organ involvements or cutaneous subgroups of SSc patients.METHOD: MPs in platelet-poor plasma from 121 patients with SSc, 79 and 42 with limited and diffuse cutaneous disease, respectively, were characterized by flow cytometry for their capacity to bind annexin V in combination with surface markers of either platelets (PMPs), leukocytes (LMPs) or endothelial cells (EMPs). Soluble E- and P-selectin levels were determined in plasma. By correlation analyses, this was held against involvement of skin, lung function, lung fibrosis, pulmonary artery hypertension, and serology.RESULTS: None of the markers were associated with cutaneous subgroups of SSc. Concentrations of annexin V non-binding EMPs and annexin V non-binding LMPs were negatively correlated to pulmonary diffusing capacity (DLCO) (r = -0.28; p = 0.003; r = -0.26; p = 0.005) and forced vital capacity (FVC) (r = -0.24; p = 0.009; r = -0.29; p = 0.002), driven by patients with limited and diffuse cutaneous disease, respectively. Soluble E-selectin levels correlated negatively to DL(CO) (r = -0.21, p = 0.03) and FVC (r = -0.25; p = 0.007); and soluble P-selectin correlated negatively to DL(CO) (r = -0.23, p = 0.01).CONCLUSION: Negative correlations between annexin V non-binding EMP and LMP concentrations with lung function parameters (DL(CO) and FVC) differed between limited and diffuse cutaneous subsets of SSc, indicative of various pathogeneses of lung involvement in SSc, possibly with a differential role of MPs.",
keywords = "Adult, Aged, Biomarkers, Cell-Derived Microparticles, Cross-Sectional Studies, E-Selectin, Female, Humans, Lung, Male, Middle Aged, P-Selectin, Scleroderma, Systemic, Skin, Young Adult",
author = "Iversen, {Line V} and Susanne Ullman and Ole {\O}stergaard and Nielsen, {Christoffer T} and Poul Halberg and Tonny Karlsmark and Heegaard, {Niels H. H.} and S{\o}ren Jacobsen",
year = "2015",
doi = "10.1186/s12891-015-0653-8",
language = "English",
volume = "16",
journal = "B M C Musculoskeletal Disorders",
issn = "1471-2474",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Cross-sectional study of soluble selectins, fractions of circulating microparticles and their relationship to lung and skin involvement in systemic sclerosis

AU - Iversen, Line V

AU - Ullman, Susanne

AU - Østergaard, Ole

AU - Nielsen, Christoffer T

AU - Halberg, Poul

AU - Karlsmark, Tonny

AU - Heegaard, Niels H. H.

AU - Jacobsen, Søren

PY - 2015

Y1 - 2015

N2 - BACKGROUND: Endothelial damage and activation may play central roles in the pathogenesis of systemic sclerosis (SSc) and are reflected by microparticles (MPs) and soluble selectins. The objective of this study was to determine if these potential biomarkers are associated with specific organ involvements or cutaneous subgroups of SSc patients.METHOD: MPs in platelet-poor plasma from 121 patients with SSc, 79 and 42 with limited and diffuse cutaneous disease, respectively, were characterized by flow cytometry for their capacity to bind annexin V in combination with surface markers of either platelets (PMPs), leukocytes (LMPs) or endothelial cells (EMPs). Soluble E- and P-selectin levels were determined in plasma. By correlation analyses, this was held against involvement of skin, lung function, lung fibrosis, pulmonary artery hypertension, and serology.RESULTS: None of the markers were associated with cutaneous subgroups of SSc. Concentrations of annexin V non-binding EMPs and annexin V non-binding LMPs were negatively correlated to pulmonary diffusing capacity (DLCO) (r = -0.28; p = 0.003; r = -0.26; p = 0.005) and forced vital capacity (FVC) (r = -0.24; p = 0.009; r = -0.29; p = 0.002), driven by patients with limited and diffuse cutaneous disease, respectively. Soluble E-selectin levels correlated negatively to DL(CO) (r = -0.21, p = 0.03) and FVC (r = -0.25; p = 0.007); and soluble P-selectin correlated negatively to DL(CO) (r = -0.23, p = 0.01).CONCLUSION: Negative correlations between annexin V non-binding EMP and LMP concentrations with lung function parameters (DL(CO) and FVC) differed between limited and diffuse cutaneous subsets of SSc, indicative of various pathogeneses of lung involvement in SSc, possibly with a differential role of MPs.

AB - BACKGROUND: Endothelial damage and activation may play central roles in the pathogenesis of systemic sclerosis (SSc) and are reflected by microparticles (MPs) and soluble selectins. The objective of this study was to determine if these potential biomarkers are associated with specific organ involvements or cutaneous subgroups of SSc patients.METHOD: MPs in platelet-poor plasma from 121 patients with SSc, 79 and 42 with limited and diffuse cutaneous disease, respectively, were characterized by flow cytometry for their capacity to bind annexin V in combination with surface markers of either platelets (PMPs), leukocytes (LMPs) or endothelial cells (EMPs). Soluble E- and P-selectin levels were determined in plasma. By correlation analyses, this was held against involvement of skin, lung function, lung fibrosis, pulmonary artery hypertension, and serology.RESULTS: None of the markers were associated with cutaneous subgroups of SSc. Concentrations of annexin V non-binding EMPs and annexin V non-binding LMPs were negatively correlated to pulmonary diffusing capacity (DLCO) (r = -0.28; p = 0.003; r = -0.26; p = 0.005) and forced vital capacity (FVC) (r = -0.24; p = 0.009; r = -0.29; p = 0.002), driven by patients with limited and diffuse cutaneous disease, respectively. Soluble E-selectin levels correlated negatively to DL(CO) (r = -0.21, p = 0.03) and FVC (r = -0.25; p = 0.007); and soluble P-selectin correlated negatively to DL(CO) (r = -0.23, p = 0.01).CONCLUSION: Negative correlations between annexin V non-binding EMP and LMP concentrations with lung function parameters (DL(CO) and FVC) differed between limited and diffuse cutaneous subsets of SSc, indicative of various pathogeneses of lung involvement in SSc, possibly with a differential role of MPs.

KW - Adult

KW - Aged

KW - Biomarkers

KW - Cell-Derived Microparticles

KW - Cross-Sectional Studies

KW - E-Selectin

KW - Female

KW - Humans

KW - Lung

KW - Male

KW - Middle Aged

KW - P-Selectin

KW - Scleroderma, Systemic

KW - Skin

KW - Young Adult

U2 - 10.1186/s12891-015-0653-8

DO - 10.1186/s12891-015-0653-8

M3 - Journal article

C2 - 26265409

VL - 16

JO - B M C Musculoskeletal Disorders

JF - B M C Musculoskeletal Disorders

SN - 1471-2474

M1 - 191

ER -

ID: 162495343