ABSTRACT
Chronic Obstructive Pulmonary Disease (COPD) is a disease of the lungs characterized by chronic airflow obstruction. Individuals with preserved ratio impaired spirometry (PRISm) may be at risk for developing COPD. This study aimed to characterize PRISm and COPD patients in terms of their immune response and endocrine profile to identify differences extending beyond lung function. The participants performed the clinical assessment, pulmonary function test, and blood collection to determine serum hormone levels and concentrations of cytokine. Differences were observed in the nutritional status, lung function, and comorbidity. There were no differences in IL-6, IL-8, IL-10, IL-12, and TNF levels between PRISm and COPD groups. Both PRISm and COPD patients have lower dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEA-S) levels than controls. Correlation analysis of PRISm and COPD patients revealed positive correlations between serum levels of DHEA-S and DHEA, with forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC), which negatively correlated with IL-8 levels. The results indicated that despite differences in lung function parameters, the PRISm and COPD groups exhibited similarities in endocrine profile alterations. This study represents the first attempt to link endocrine with immune markers and lung function in individuals with PRISm.
Subject(s)
Biomarkers , Pulmonary Disease, Chronic Obstructive , Spirometry , Humans , Pulmonary Disease, Chronic Obstructive/blood , Male , Female , Biomarkers/blood , Middle Aged , Aged , Cytokines/blood , Dehydroepiandrosterone/blood , Inflammation/blood , Dehydroepiandrosterone Sulfate/blood , Vital Capacity , Respiratory Function Tests , Forced Expiratory VolumeABSTRACT
BACKGROUND: Visceral leishmaniasis (VL) is a tropical neglected disease with high associated rates of mortality. Several studies have highlighted the importance of the intestinal tract (IT) and gut microbiota (GM) in the host immunological defense. Data in the literature on parasite life cycle and host immune defense against VL are scarce regarding the effects of infection on the IT and GM. OBJECTIVES: This study aimed to investigate changes observed in the colon of Leishmania infantum-infected hamsters, including alterations in the enteric nervous system (ENS) and GM (specifically, levels of bifidobacteria and lactobacilli). METHODS: Male hamsters were inoculated with L. infantum and euthanised at four or eight months post-infection. Intestines were processed for histological analysis and GM analysis. Quantitative polymerase chain reaction (qPCR) was performed to quantify each group of bacteria: Bifidobacterium spp. (Bf) and Lactobacillus spp (LacB). FINDINGS: Infected hamsters showed histoarchitectural loss in the colon wall, with increased thickness in the submucosa and the mucosa layer, as well as greater numbers of intraepithelial lymphocytes. Forms suggestive of amastigotes were seen inside mononuclear cells. L. infantum infection induced changes in ENS, as evidenced by increases in the area of colonic enteric ganglia. Despite the absence of changes in the levels of Bf and LacB during the course of infection, the relative abundance of these bacteria was associated with parasite load and histological alterations. MAIN CONCLUSIONS: Our results indicate that L. infantum infection leads to important changes in the colon and suggest that bacteria in the GM play a protective role.
Subject(s)
Bifidobacterium , Gastrointestinal Microbiome , Lactobacillus , Leishmania infantum , Leishmaniasis, Visceral , Animals , Cricetinae , Intestines/parasitology , Parasite LoadABSTRACT
Introduction: studies have highlighted the importance of gut microbiota (GM) to the host immune defenses, influencing the host development and physiology. Changes in the composition and diversity of GM have been detected in some disease and could be implicated in the pathophysiological mechanisms of them. Objective: the purpose of this study was to show an overview of the current knowledge about the GM of patients with airway diseases (AD). Methodology: the literature search was performed in four databases, using a combination of the descriptors: "Gastrointestinal Microbiome", "Gut Microbiome", "Gut Microbiota", "Cystic Fibrosis" (CF), "Asthma", "Pulmonary Hypertension" (HP) and/or "Chronic Obstructive Pulmonary Disease" (COPD). Results: fifteen studies were herein included: ten of CF and five of asthma. No study about other AD matched the inclusion criteria. In all studies about CF, changes were detected in GM, particularly quantitative and qualitative microbial changes. For asthma, data showed changes in GM also including a reduction of microbial richness, evenness and diversity and in the Bacteroidetes/Firmicutes ratio. Conclusions: the current data indicate the existence of GM changes in AD. However, due to the few studies for asthma and the lack of investigations on HP and COPD, it was not possible to confirm whether these GM changes are observed in other AD. Furthermore, this review shows the necessity of more studies in this area to characterize dysbiosis and which alterations are more frequent observed in AD patients.
Introdução: estudos têm destacado a importância da microbiota intestinal (GM) para as defesas imunológicas do hospedeiro, influenciando o desenvolvimento e a fisiologia do hospedeiro. Mudanças na composição e diversidade da GM foram detectadas em algumas doenças e podem estar implicadas nos mecanismos fisiopatológicos delas. Objetivo: o objetivo desta revisão foi avaliar estudos sobre a microbiota intestinal (MI) de pacientes com doenças das vias aéreas (DA). Metodologia: esta pesquisa bibliográfica foi realizada em quatro bases de dados, utilizando a combinação dos descritores: "Microbioma Gastrointestinal", "Microbioma Intestinal", "Microbiota Intestinal", "Fibrose Cística" (CF), "Asma", "Hipertensão Pulmonar" (HP), "Doença Pulmonar Obstrutiva Crônica" (DPOC). Resultados: quinze estudos foram incluídos: dez de FC e cinco de asma. Nenhum estudo sobre outra DA correspondeu aos critérios de inclusão. Em todos os estudos sobre FC, foram detectadas alterações na MI, particularmente alterações microbianas qualitativas e quantitativas. Para a asma, os dados mostraram mudanças na MI, incluindo também uma redução da quantidade, uniformidade e diversidade microbiana e na razão Bacteroidetes/Firmicutes. Conclusão: os dados atuais indicam a existência de alterações na MI nas DA. No entanto, devido aos poucos estudos para asma e à falta de investigações para HP e DPOC, não foi possível confirmar se essas alterações na MI são observadas em outras DA também. Além disso, esta revisão mostra a necessidade de mais estudos nessa área para caracterizar a disbiose e quais alterações são mais frequentes em pacientes com DA.
