The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection

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The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection. / Hansen, Marco Bo; Rasmussen, Lars S; Pilely, Katrine; Hellemann, Dorthe; Hein, Estrid; Madsen, Martin Bruun; Hyldegaard, Ole; Garred, Peter.

In: Journal of Innate Immunity, Vol. 8, No. 5, 2016, p. 507-16.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hansen, MB, Rasmussen, LS, Pilely, K, Hellemann, D, Hein, E, Madsen, MB, Hyldegaard, O & Garred, P 2016, 'The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection', Journal of Innate Immunity, vol. 8, no. 5, pp. 507-16. https://doi.org/10.1159/000447327

APA

Hansen, M. B., Rasmussen, L. S., Pilely, K., Hellemann, D., Hein, E., Madsen, M. B., Hyldegaard, O., & Garred, P. (2016). The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection. Journal of Innate Immunity, 8(5), 507-16. https://doi.org/10.1159/000447327

Vancouver

Hansen MB, Rasmussen LS, Pilely K, Hellemann D, Hein E, Madsen MB et al. The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection. Journal of Innate Immunity. 2016;8(5):507-16. https://doi.org/10.1159/000447327

Author

Hansen, Marco Bo ; Rasmussen, Lars S ; Pilely, Katrine ; Hellemann, Dorthe ; Hein, Estrid ; Madsen, Martin Bruun ; Hyldegaard, Ole ; Garred, Peter. / The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection. In: Journal of Innate Immunity. 2016 ; Vol. 8, No. 5. pp. 507-16.

Bibtex

@article{7f4718043cac43919b683629248316fd,
title = "The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection",
abstract = "BACKGROUND: Mannose-binding lectin (MBL) and ficolins are pattern recognition molecules (PRMs) that play an important role during infection through activation of the lectin complement pathway. We assessed whether plasma PRM levels were associated with mortality in patients with necrotizing soft tissue infection (NSTI).METHODS: We conducted a prospective, observational study over 25 months involving 135 NSTI patients with a maximum follow-up of 2.7 years. Blood samples were taken upon admission. Non-infected patients served as controls.RESULTS: PRM levels were significantly lower compared with controls. A baseline Ficolin-2 level below the median was associated with mortality at the end of follow-up (p = 0.007). No significant association was found for MBL, Ficolin-1 and Ficolin-3. A Ficolin-2 level below the median had a negative predictive value of 0.94 for 28-day mortality, and a level below the optimal cut-off was independently associated with 28-day mortality when adjusted for age, sex and chronicity [hazard ratio 6.27 (95% confidence interval 2.28-17.21), p < 0.0001], also when Simplified Acute Physiology Score II was included in the analysis [hazard ratio 3.16 (95% confidence interval 1.03-9.73), p = 0.045].CONCLUSIONS: All PRMs were significantly lower in patients with NSTI than in controls. Only baseline Ficolin-2 was associated with short- and long-term mortality. A high baseline Ficolin-2 level indicated a 94% chance of surviving the first 28 days after admission.",
keywords = "Journal Article",
author = "Hansen, {Marco Bo} and Rasmussen, {Lars S} and Katrine Pilely and Dorthe Hellemann and Estrid Hein and Madsen, {Martin Bruun} and Ole Hyldegaard and Peter Garred",
note = "{\textcopyright} 2016 S. Karger AG, Basel.",
year = "2016",
doi = "10.1159/000447327",
language = "English",
volume = "8",
pages = "507--16",
journal = "Journal of Innate Immunity",
issn = "1662-811X",
publisher = "S Karger AG",
number = "5",

}

RIS

TY - JOUR

T1 - The Lectin Complement Pathway in Patients with Necrotizing Soft Tissue Infection

AU - Hansen, Marco Bo

AU - Rasmussen, Lars S

AU - Pilely, Katrine

AU - Hellemann, Dorthe

AU - Hein, Estrid

AU - Madsen, Martin Bruun

AU - Hyldegaard, Ole

AU - Garred, Peter

N1 - © 2016 S. Karger AG, Basel.

PY - 2016

Y1 - 2016

N2 - BACKGROUND: Mannose-binding lectin (MBL) and ficolins are pattern recognition molecules (PRMs) that play an important role during infection through activation of the lectin complement pathway. We assessed whether plasma PRM levels were associated with mortality in patients with necrotizing soft tissue infection (NSTI).METHODS: We conducted a prospective, observational study over 25 months involving 135 NSTI patients with a maximum follow-up of 2.7 years. Blood samples were taken upon admission. Non-infected patients served as controls.RESULTS: PRM levels were significantly lower compared with controls. A baseline Ficolin-2 level below the median was associated with mortality at the end of follow-up (p = 0.007). No significant association was found for MBL, Ficolin-1 and Ficolin-3. A Ficolin-2 level below the median had a negative predictive value of 0.94 for 28-day mortality, and a level below the optimal cut-off was independently associated with 28-day mortality when adjusted for age, sex and chronicity [hazard ratio 6.27 (95% confidence interval 2.28-17.21), p < 0.0001], also when Simplified Acute Physiology Score II was included in the analysis [hazard ratio 3.16 (95% confidence interval 1.03-9.73), p = 0.045].CONCLUSIONS: All PRMs were significantly lower in patients with NSTI than in controls. Only baseline Ficolin-2 was associated with short- and long-term mortality. A high baseline Ficolin-2 level indicated a 94% chance of surviving the first 28 days after admission.

AB - BACKGROUND: Mannose-binding lectin (MBL) and ficolins are pattern recognition molecules (PRMs) that play an important role during infection through activation of the lectin complement pathway. We assessed whether plasma PRM levels were associated with mortality in patients with necrotizing soft tissue infection (NSTI).METHODS: We conducted a prospective, observational study over 25 months involving 135 NSTI patients with a maximum follow-up of 2.7 years. Blood samples were taken upon admission. Non-infected patients served as controls.RESULTS: PRM levels were significantly lower compared with controls. A baseline Ficolin-2 level below the median was associated with mortality at the end of follow-up (p = 0.007). No significant association was found for MBL, Ficolin-1 and Ficolin-3. A Ficolin-2 level below the median had a negative predictive value of 0.94 for 28-day mortality, and a level below the optimal cut-off was independently associated with 28-day mortality when adjusted for age, sex and chronicity [hazard ratio 6.27 (95% confidence interval 2.28-17.21), p < 0.0001], also when Simplified Acute Physiology Score II was included in the analysis [hazard ratio 3.16 (95% confidence interval 1.03-9.73), p = 0.045].CONCLUSIONS: All PRMs were significantly lower in patients with NSTI than in controls. Only baseline Ficolin-2 was associated with short- and long-term mortality. A high baseline Ficolin-2 level indicated a 94% chance of surviving the first 28 days after admission.

KW - Journal Article

U2 - 10.1159/000447327

DO - 10.1159/000447327

M3 - Journal article

C2 - 27355483

VL - 8

SP - 507

EP - 516

JO - Journal of Innate Immunity

JF - Journal of Innate Immunity

SN - 1662-811X

IS - 5

ER -

ID: 176966875