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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Lactate dehydrogenase isoenzymes in patients with acute exacerbation of chronic obstructive pulmonary disease: An exploratory cross-sectional study

Thumbnail
Συγγραφέας
Skopas V., Papadopoulos D., Trakas N., Papaefstathiou E., Koufopoulos C., Makris D., Daniil Z., Gourgoulianis K.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1016/j.resp.2020.103562
Λέξη-κλειδί
lactate dehydrogenase 1
lactate dehydrogenase 2
lactate dehydrogenase 3
lactate dehydrogenase 4
lactate dehydrogenase A
lactate dehydrogenase isoenzyme
unclassified drug
biological marker
isoenzyme
lactate dehydrogenase
acute disease
aerobic metabolism
aged
arterial gas
Article
chronic obstructive lung disease
controlled study
cross-sectional study
disease exacerbation
electrophoresis
exploratory research
female
hospital patient
human
lactate dehydrogenase blood level
lower respiratory tract infection
major clinical study
male
pilot study
priority journal
acute disease
adult
blood
chronic obstructive lung disease
differential diagnosis
middle aged
recurrent disease
respiratory tract infection
sensitivity and specificity
very elderly
Acute Disease
Adult
Aged
Aged, 80 and over
Biomarkers
Cross-Sectional Studies
Diagnosis, Differential
Female
Humans
Isoenzymes
L-Lactate Dehydrogenase
Male
Middle Aged
Pilot Projects
Pulmonary Disease, Chronic Obstructive
Respiratory Tract Infections
Sensitivity and Specificity
Symptom Flare Up
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
We aimed to evaluate differences in serum lactate dehydrogenase (LDH) isoenzymes between patients hospitalized for acute exacerbation of chronic obstructive pulmonary disease (AECOPD) and other lower respiratory tract infections (LRTIs). Based on self-reported COPD diagnosis, 71 participants were divided into AECOPD (n = 38, 29 males, mean age 70.5 years) and LRTI (n = 33, 12 males, mean age 70.4 years) groups. Information on demographics, comorbidities, and COPD severity markers, as well as arterial blood gases and laboratory data were collected, while serum LDH electrophoresis was performed to examine the LDH isoenzymes. Adjusting for sex, age, comorbidities, degree of hypoxemia, inflammation markers, muscle and myocardial enzymes, and total serum LDH, the mean differences (95 % confidence intervals) in the ratios of serum LDH isoenzymes to total serum LDH between groups (LDHxAECOPD − LDHxLRTI) were statistically significant for LDH1 [4.9 (1.4 to 8.3)], LDH2 [3.0 (0.1 to 5.8)], LDH3 [−4.3 (−6.3 to −2.3)], and LDH4 [−3.2 (−4.9 to −1.5)]. A sum of LDH3 and LDH4 ratios below 29 % had the highest discriminative ability to classify a subject in the AECOPD group (AUC 0.841, sensitivity 76 %, specificity 87 %). Aerobic metabolic adaptive mechanisms in respiratory muscles during AECOPD could explain the above differences. © 2020 Elsevier B.V.
URI
http://hdl.handle.net/11615/79092
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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