Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting

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Standard

Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting. / Bastrup-Birk, S; Munthe-Fog, L; Skjødt, Mikkel-Ole; Ma, Y J; Nielsen, H; Køber, L; Nielsen, O W; Iversen, K; Garred, P.

In: Journal of Internal Medicine, Vol. 277, No. 5, 05.2015, p. 562-572.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bastrup-Birk, S, Munthe-Fog, L, Skjødt, M-O, Ma, YJ, Nielsen, H, Køber, L, Nielsen, OW, Iversen, K & Garred, P 2015, 'Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting', Journal of Internal Medicine, vol. 277, no. 5, pp. 562-572. https://doi.org/10.1111/joim.12294

APA

Bastrup-Birk, S., Munthe-Fog, L., Skjødt, M-O., Ma, Y. J., Nielsen, H., Køber, L., Nielsen, O. W., Iversen, K., & Garred, P. (2015). Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting. Journal of Internal Medicine, 277(5), 562-572. https://doi.org/10.1111/joim.12294

Vancouver

Bastrup-Birk S, Munthe-Fog L, Skjødt M-O, Ma YJ, Nielsen H, Køber L et al. Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting. Journal of Internal Medicine. 2015 May;277(5):562-572. https://doi.org/10.1111/joim.12294

Author

Bastrup-Birk, S ; Munthe-Fog, L ; Skjødt, Mikkel-Ole ; Ma, Y J ; Nielsen, H ; Køber, L ; Nielsen, O W ; Iversen, K ; Garred, P. / Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting. In: Journal of Internal Medicine. 2015 ; Vol. 277, No. 5. pp. 562-572.

Bibtex

@article{efed4b9447ab4860b4398291124177c4,
title = "Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting",
abstract = "BACKGROUND: The pattern recognition molecule pentraxin-3 (PTX3) is a novel potential marker of prognosis, as elevated levels are associated with both disease severity and mortality in patients with a wide range of conditions. However, the usefulness of PTX3 as a prognostic biomarker in a general hospital setting is unknown.PATIENTS AND METHODS: The study cohort consisted of 1326 unselected, consecutive patients (age >40 years) admitted to a community hospital in Copenhagen, Denmark. Patients were followed until death or for a median of 11.5 years after admission. The main outcome measure was all-cause mortality. Serum samples collected from patients at admission and from 192 healthy control subjects were quantified for PTX3 level by enzyme-linked immunosorbent assay.RESULTS: PTX3 was elevated in patients (median 3.7 ng mL(-1) , range 0.5-209.8) compared with healthy nonhospitalized subjects (median 3.5 ng mL(-1) , range 0.0-8.3; P = 0.0003). Elevated PTX3 levels, defined as above the 95th percentile of the concentration in healthy subjects, were associated with increased overall mortality during the study (P < 0.0001). This increase in mortality was greatest in the short term, with an unadjusted hazard ratio (HR) of 6.4 [95% confidence interval (CI) 3.8-11.0] at 28 days after admission, compared to 1.7 (95% CI 1.4-2.0) at the end of follow-up. These results were still significant after adjustment for age, gender and glomerular filtration rate: adjusted HR of 5.0 (95% CI 2.9-8.8) and 1.4 (95% CI 1.2-1.8), respectively.CONCLUSION: These results suggest that PTX3 could be a widely applicable marker of short-term mortality in hospitalized patients and may be useful in the initial risk stratification.",
keywords = "Aged, Biomarkers, C-Reactive Protein, Case-Control Studies, Denmark, Female, Hospital Mortality, Hospitalization, Hospitals, Community, Humans, Kaplan-Meier Estimate, Male, Prognosis, Serum Amyloid P-Component",
author = "S Bastrup-Birk and L Munthe-Fog and Mikkel-Ole Skj{\o}dt and Ma, {Y J} and H Nielsen and L K{\o}ber and Nielsen, {O W} and K Iversen and P Garred",
note = "{\textcopyright} 2014 The Association for the Publication of the Journal of Internal Medicine.",
year = "2015",
month = may,
doi = "10.1111/joim.12294",
language = "English",
volume = "277",
pages = "562--572",
journal = "Acta Medica Scandinavica",
issn = "0955-7873",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Pentraxin-3 level at admission is a strong predictor of short-term mortality in a community-based hospital setting

AU - Bastrup-Birk, S

AU - Munthe-Fog, L

AU - Skjødt, Mikkel-Ole

AU - Ma, Y J

AU - Nielsen, H

AU - Køber, L

AU - Nielsen, O W

AU - Iversen, K

AU - Garred, P

N1 - © 2014 The Association for the Publication of the Journal of Internal Medicine.

PY - 2015/5

Y1 - 2015/5

N2 - BACKGROUND: The pattern recognition molecule pentraxin-3 (PTX3) is a novel potential marker of prognosis, as elevated levels are associated with both disease severity and mortality in patients with a wide range of conditions. However, the usefulness of PTX3 as a prognostic biomarker in a general hospital setting is unknown.PATIENTS AND METHODS: The study cohort consisted of 1326 unselected, consecutive patients (age >40 years) admitted to a community hospital in Copenhagen, Denmark. Patients were followed until death or for a median of 11.5 years after admission. The main outcome measure was all-cause mortality. Serum samples collected from patients at admission and from 192 healthy control subjects were quantified for PTX3 level by enzyme-linked immunosorbent assay.RESULTS: PTX3 was elevated in patients (median 3.7 ng mL(-1) , range 0.5-209.8) compared with healthy nonhospitalized subjects (median 3.5 ng mL(-1) , range 0.0-8.3; P = 0.0003). Elevated PTX3 levels, defined as above the 95th percentile of the concentration in healthy subjects, were associated with increased overall mortality during the study (P < 0.0001). This increase in mortality was greatest in the short term, with an unadjusted hazard ratio (HR) of 6.4 [95% confidence interval (CI) 3.8-11.0] at 28 days after admission, compared to 1.7 (95% CI 1.4-2.0) at the end of follow-up. These results were still significant after adjustment for age, gender and glomerular filtration rate: adjusted HR of 5.0 (95% CI 2.9-8.8) and 1.4 (95% CI 1.2-1.8), respectively.CONCLUSION: These results suggest that PTX3 could be a widely applicable marker of short-term mortality in hospitalized patients and may be useful in the initial risk stratification.

AB - BACKGROUND: The pattern recognition molecule pentraxin-3 (PTX3) is a novel potential marker of prognosis, as elevated levels are associated with both disease severity and mortality in patients with a wide range of conditions. However, the usefulness of PTX3 as a prognostic biomarker in a general hospital setting is unknown.PATIENTS AND METHODS: The study cohort consisted of 1326 unselected, consecutive patients (age >40 years) admitted to a community hospital in Copenhagen, Denmark. Patients were followed until death or for a median of 11.5 years after admission. The main outcome measure was all-cause mortality. Serum samples collected from patients at admission and from 192 healthy control subjects were quantified for PTX3 level by enzyme-linked immunosorbent assay.RESULTS: PTX3 was elevated in patients (median 3.7 ng mL(-1) , range 0.5-209.8) compared with healthy nonhospitalized subjects (median 3.5 ng mL(-1) , range 0.0-8.3; P = 0.0003). Elevated PTX3 levels, defined as above the 95th percentile of the concentration in healthy subjects, were associated with increased overall mortality during the study (P < 0.0001). This increase in mortality was greatest in the short term, with an unadjusted hazard ratio (HR) of 6.4 [95% confidence interval (CI) 3.8-11.0] at 28 days after admission, compared to 1.7 (95% CI 1.4-2.0) at the end of follow-up. These results were still significant after adjustment for age, gender and glomerular filtration rate: adjusted HR of 5.0 (95% CI 2.9-8.8) and 1.4 (95% CI 1.2-1.8), respectively.CONCLUSION: These results suggest that PTX3 could be a widely applicable marker of short-term mortality in hospitalized patients and may be useful in the initial risk stratification.

KW - Aged

KW - Biomarkers

KW - C-Reactive Protein

KW - Case-Control Studies

KW - Denmark

KW - Female

KW - Hospital Mortality

KW - Hospitalization

KW - Hospitals, Community

KW - Humans

KW - Kaplan-Meier Estimate

KW - Male

KW - Prognosis

KW - Serum Amyloid P-Component

U2 - 10.1111/joim.12294

DO - 10.1111/joim.12294

M3 - Journal article

C2 - 25143177

VL - 277

SP - 562

EP - 572

JO - Acta Medica Scandinavica

JF - Acta Medica Scandinavica

SN - 0955-7873

IS - 5

ER -

ID: 152268299