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Increased monocyte count and red cell distribution width as prognostic biomarkers in patients with Idiopathic Pulmonary Fibrosis

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Συγγραφέας
Karampitsakos T., Torrisi S., Antoniou K., Manali E., Korbila I., Papaioannou O., Sampsonas F., Katsaras M., Vasarmidi E., Papakosta D., Domvri K., Fouka E., Organtzis I., Daniil Z., Dimeas I., Kirgou P., Gourgoulianis K.I., Papanikolaou I.C., Markopoulou K., Kounti G., Tsapakidou E., Papadopoulou E., Tatsis K., Gogali A., Kostikas K., Tzilas V., Chrysikos S., Papiris S., Bouros D., Kreuter M., Tzouvelekis A.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1186/s12931-021-01725-9
Λέξη-κλειδί
nintedanib
pirfenidone
aged
all cause mortality
Article
cohort analysis
diffusing capacity for carbon monoxide
disease exacerbation
female
fibrosing alveolitis
forced vital capacity
human
Kaplan Meier method
major clinical study
male
monocyte count
observational study
oxygen therapy
prognosis
red blood cell distribution width
retrospective study
risk factor
blood
clinical trial
epidemiology
erythrocyte
fibrosing alveolitis
Greece
leukocyte count
lung
mean corpuscular volume
monocyte
mortality
multicenter study
pathophysiology
predictive value
prognosis
reproducibility
vital capacity
Aged
Erythrocyte Indices
Erythrocytes
Female
Greece
Humans
Idiopathic Pulmonary Fibrosis
Leukocyte Count
Lung
Male
Monocytes
Predictive Value of Tests
Prognosis
Reproducibility of Results
Retrospective Studies
Vital Capacity
BioMed Central Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Background: Idiopathic Pulmonary Fibrosis (IPF) represents a chronic lung disease with unpredictable course. Methods: We aimed to investigate prognostic performance of complete blood count parameters in IPF. Treatment-naïve patients with IPF were retrospectively enrolled from two independent cohorts (derivation and validation) and split into subgroups (high and low) based on median baseline monocyte count and red cell distribution width (RDW). Results: Overall, 489 patients (derivation cohort: 300, validation cohort: 189) were analyzed. In the derivation cohort, patients with monocyte count ≥ 0.60 K/μL had significantly lower median FVC%pred [75.0, (95% CI 71.3–76.7) vs. 80.9, (95% CI 77.5–83.1), (P = 0.01)] and DLCO%pred [47.5, (95% CI 44.3–52.3) vs. 53.0, (95% CI 48.0–56.7), (P = 0.02)] than patients with monocyte count < 0.60 K/μL. Patients with RDW ≥ 14.1% had significantly lower median FVC%pred [75.5, (95% CI 71.2–79.2) vs. 78.3, (95% CI 76.0–81.0), (P = 0.04)] and DLCO%pred [45.4, (95% CI 43.3–50.5) vs. 53.0, (95% CI 50.8–56.8), (P = 0.008)] than patients with RDW < 14.1%. Cut-off thresholds from the derivation cohort were applied to the validation cohort with similar discriminatory value, as indicated by significant differences in median DLCO%pred between patients with high vs. low monocyte count [37.8, (95% CI 35.5–41.1) vs. 45.5, (95% CI 41.9–49.4), (P < 0.001)] and RDW [37.9, (95% CI 33.4–40.7) vs. 44.4, (95% CI 41.5–48.9), (P < 0.001)]. Patients with high monocyte count and RDW of the validation cohort exhibited a trend towards lower median FVC%pred (P = 0.09) and significantly lower median FVC%pred (P = 0.001), respectively. Kaplan–Meier analysis in the derivation cohort demonstrated higher all-cause mortality in patients with high (≥ 0.60 K/μL) vs. low monocyte count (< 0.60 K/μL) [HR 2.05, (95% CI 1.19–3.53), (P = 0.01)]. Conclusions: Increased monocyte count and RDW may represent negative prognostic biomarkers in patients with IPF. © 2021, The Author(s).
URI
http://hdl.handle.net/11615/74410
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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