The characteristics of the frequent exacerbator with chronic bronchitis phenotype and non-exacerbator phenotype in patients with chronic obstructive pulmonary disease: a meta-analysis and system review
Abstract:Background: Chronic obstructive pulmonary disease (COPD) patients with different phenotypes show different clinical characteristics. Therefore, we conducted a meta-analysis to explore the clinical characteristics between the non-exacerbator (NE) phenotype and the frequent exacerbator with chronic bronchitis (FE-CB) phenotype among patients with COPD. Methods: CNKI, Wan fang, Chongqing VIP, China Biology Medicine disc, PubMed, Cochrane Library, and EMBASE databases were searched from the times of their inceptio… Show more
“…The results demonstrated that caT scores, mMrc scores and nlr levels were significantly higher in the COPD-FE group compared with those in the COPD-FE group (Table I). These findings align with prior research in showing similar expression trends of these indicators in COPD-FE patients (9)(10)(11). Furthermore, the SF-36 questionnaire was used to assess disease impact demonstrating significantly lower scores in PF, RP, GH, VT and SF for the coPd-Fe group compared with those in the coPd-ne group; however, BP, re, MH and HT scores did not demonstrate a significant difference (Table I).…”
Section: Resultssupporting
confidence: 88%
“…Therefore, the central focus of coPd management during stable periods revolves around averting acute exacerbations and reducing their frequency. numerous clinical predictors of acute exacerbation risk in coPd have been assessed, including low body mass index (BMI) (7), deteriorating lung function (8), increased COPD assessment test (CAT) scores (9), modified Medical Research council (mMrc) dyspnea scale scores (10), and elevated neutrophil-to-lymphocyte ratio (nlr) and platelet-to-lymphocyte ratio (Plr) (11). However, predicting coPd-Fe risk and understanding its underlying pathogenic mechanisms remains challenging due to the heterogeneity and complexity of coPd.…”
Section: Serum Metabolomics Analysis Of Patients With Chronic Obstruc...mentioning
“…The results demonstrated that caT scores, mMrc scores and nlr levels were significantly higher in the COPD-FE group compared with those in the COPD-FE group (Table I). These findings align with prior research in showing similar expression trends of these indicators in COPD-FE patients (9)(10)(11). Furthermore, the SF-36 questionnaire was used to assess disease impact demonstrating significantly lower scores in PF, RP, GH, VT and SF for the coPd-Fe group compared with those in the coPd-ne group; however, BP, re, MH and HT scores did not demonstrate a significant difference (Table I).…”
Section: Resultssupporting
confidence: 88%
“…Therefore, the central focus of coPd management during stable periods revolves around averting acute exacerbations and reducing their frequency. numerous clinical predictors of acute exacerbation risk in coPd have been assessed, including low body mass index (BMI) (7), deteriorating lung function (8), increased COPD assessment test (CAT) scores (9), modified Medical Research council (mMrc) dyspnea scale scores (10), and elevated neutrophil-to-lymphocyte ratio (nlr) and platelet-to-lymphocyte ratio (Plr) (11). However, predicting coPd-Fe risk and understanding its underlying pathogenic mechanisms remains challenging due to the heterogeneity and complexity of coPd.…”
Section: Serum Metabolomics Analysis Of Patients With Chronic Obstruc...mentioning
“…Previous studies found that the exacerbator phenotype mainly exacerbator chronic bronchitis had the highest CAT score [5,17]. A meta-analysis study found that in ten studies that included 4568 patients, the frequent exacerbator of chronic bronchitis phenotype was associated with a high CAT score than in the ACO phenotype [18].…”
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“…Обострением считают ухудшение респираторных симптомов, выходящее за рамки обычных ежедневных колебаний, продолжающееся более 2 последовательных суток и требующее интенсификации терапии [1]. Доказана взаимосвязь обострений с риском смерти, инвалидизацией больных, тяжестью ограничения воздушного потока, снижением качества жизни, коморбидными состояниями, увеличением затрат на лечение [3,4]. Распространенность фенотипа ХОБЛ с обострениями сос тавляет 33,7% [5].…”
Aim. To establish symptoms, lung function and to evaluate subsequent exacerbations of chronic obstructive pulmonary disease (COPD) during a year after virus-induced COPD exacerbations.
Materials and methods. Patients hospitalized with viral (n=60), bacterial (n=60) and viral-bacterial (n=60) COPD exacerbations were enrolled to single-center prospective observational study. COPD was diagnosed according spirography criteria. Viral infection was established in bronchoalveolar lavage fluid or sputum by real-time reverse transcription-polymerase chain reaction for RNA of influenza A and B virus, rhinovirus, respiratory syncytial virus and SARS-CoV-2. Symptoms, lung function, COPD exacerbations were assessed. Patients were investigated at the hospitalization onset and then 4 and 52 weeks following the discharge from the hospital.
Results. After 52 weeks in viral and viral-bacterial COPD exacerbations groups the rate of forced expiratory volume in one second (FEV1) decline were maximal 71 (68; 73) ml/year and 69 (67; 72) ml/year versus 59 (55; 62) ml/year after bacterial exacerbations. Low levels of diffusion lung capacity for carbon monoxide (DLco/Va) 52.5% (45.1%; 55.8%), 50.2% (44.9%; 56.0%) and 75.3% (72.2%; 80.1%) respectively, of 6-minute walk distance; p0.001 in relation to bacterial exacerbations. In Cox proportional hazards regression analyses viral and viral-bacterial exacerbations were associated with increased risk of subsequent COPD exacerbations by 2.4 times independent of exacerbations rate before index event and FEV1. In linear regression models the relationships between airflow limitation and respiratory syncytial virus, rhinovirus and influenza virus infection, between low DLco/Va and rhinovirus, influenza virus and SARS-CoV-2 infection.
Conclusion. COPD after virus-induced exacerbations were characterized by progression of airflow limitation, low DLco/Va, low 6-minute walking test distance, subsequent COPD exacerbations risk.
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