Neutrophil count in sputum is associated with increased sputum glucose and sputum L-lactate in cystic fibrosis
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Neutrophil count in sputum is associated with increased sputum glucose and sputum L-lactate in cystic fibrosis. / Nielsen, Bibi Uhre; Kolpen, Mette; Jensen, Peter Østrup; Katzenstein, Terese; Pressler, Tacjana; Ritz, Christian; Mathiesen, Inger Hee Mabuza; Faurholt-Jepsen, Daniel.
In: P L o S One, Vol. 15, No. 9, e0238524, 2020.Research output: Contribution to journal › Journal article › Research › peer-review
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T1 - Neutrophil count in sputum is associated with increased sputum glucose and sputum L-lactate in cystic fibrosis
AU - Nielsen, Bibi Uhre
AU - Kolpen, Mette
AU - Jensen, Peter Østrup
AU - Katzenstein, Terese
AU - Pressler, Tacjana
AU - Ritz, Christian
AU - Mathiesen, Inger Hee Mabuza
AU - Faurholt-Jepsen, Daniel
N1 - CURIS 2020 NEXS 295
PY - 2020
Y1 - 2020
N2 - Background: Markers of lung inflammation measured directly in expectorated sputum have the potential of improving the timing of antibiotic treatment in cystic fibrosis (CF). L-Lactate might be a marker of inflammation, as it is produced from glucose by polymorphonuclear neutrophils (PMNs) in CF lungs. We aimed to investigate changes in and associations between PMNs, glucose and L-lactate in sputum during antibiotic treatment. In addition, the effect of hemoglobin A1c and plasma glucose on these biomarkers were investigated.Methods: We sampled non-induced sputum at day 0, 7, 14 and 42 in 27 chronically infected CF patients electively treated with 14 days of intravenous antibiotic. To analyze sputum samples, we used flowcytometry to count PMNs and colorimetric assays to estimate lactate and glucose.Results: No changes in levels of PMNs, glucose and lactate were detected in sputum during the antibiotic treatment. Sputum PMNs were positively associated with both glucose (log coefficient = 0.20, p = 0.01) and L-lactate (log coefficient = 0.34, p<0.001). In multivariate analyses, hemoglobin A1c was negatively associated with sputum PMNs (log coefficient = -1.68, p<0.001) and plasma glucose was negatively associated with sputum glucose (log coefficient = -0.09, p = 0.02).Conclusions: In CF sputum PMNs, glucose and lactate were unchanged during elective antibiotic treatment. However, sputum PMNs were associated with both sputum glucose and sputum lactate. Surprisingly, hyperglycemia seemed to be associated with less PMNs infiltration and less glucose in CF sputum.
AB - Background: Markers of lung inflammation measured directly in expectorated sputum have the potential of improving the timing of antibiotic treatment in cystic fibrosis (CF). L-Lactate might be a marker of inflammation, as it is produced from glucose by polymorphonuclear neutrophils (PMNs) in CF lungs. We aimed to investigate changes in and associations between PMNs, glucose and L-lactate in sputum during antibiotic treatment. In addition, the effect of hemoglobin A1c and plasma glucose on these biomarkers were investigated.Methods: We sampled non-induced sputum at day 0, 7, 14 and 42 in 27 chronically infected CF patients electively treated with 14 days of intravenous antibiotic. To analyze sputum samples, we used flowcytometry to count PMNs and colorimetric assays to estimate lactate and glucose.Results: No changes in levels of PMNs, glucose and lactate were detected in sputum during the antibiotic treatment. Sputum PMNs were positively associated with both glucose (log coefficient = 0.20, p = 0.01) and L-lactate (log coefficient = 0.34, p<0.001). In multivariate analyses, hemoglobin A1c was negatively associated with sputum PMNs (log coefficient = -1.68, p<0.001) and plasma glucose was negatively associated with sputum glucose (log coefficient = -0.09, p = 0.02).Conclusions: In CF sputum PMNs, glucose and lactate were unchanged during elective antibiotic treatment. However, sputum PMNs were associated with both sputum glucose and sputum lactate. Surprisingly, hyperglycemia seemed to be associated with less PMNs infiltration and less glucose in CF sputum.
U2 - 10.1371/journal.pone.0238524
DO - 10.1371/journal.pone.0238524
M3 - Journal article
C2 - 32915806
VL - 15
JO - PLoS ONE
JF - PLoS ONE
SN - 1932-6203
IS - 9
M1 - e0238524
ER -
ID: 248545672