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Master's Dissertation
DOI
https://doi.org/10.11606/D.5.2001.tde-17022002-163819
Document
Author
Full name
Denis Pajecki
E-mail
Institute/School/College
Knowledge Area
Date of Defense
Published
São Paulo, 2001
Supervisor
Committee
Zilberstein, Bruno (President)
Gagliardi, Danilo
Nasi, Ary
Title in Portuguese
Microbiota no megaesôfago chagásico.
Keywords in Portuguese
Acalasia
Acalasia esofágica/microbiologia
Composto nitroso/análise
Doença de Chagas/etiologia
Megaesôfago
Microbiologia
Nitrato reductases/análise
Abstract in Portuguese
A estase de secreção salivar e alimentos deglutidos na luz esofágica de pacientes com megaesôfago chagásico traz como consequências: (1) supercrescimento bacteriano na luz do órgão, (2) episódios de aspiração pulmonar e infecções respiratórias de repetição, (3) aumento do risco dos procedimentos terapêuticos cirúrgicos ou endoscópicos em caso de perfuração pela maior possibilidade de contaminação, (4) desenvolvimento de processos inflamatórios crônicos na mucosa esofágica, que podem predispor ao aparecimento de displasia e câncer. Apesar disto, a microbita esofágica no megaesôfago nunca foi estudado. Esse estudo teve o objetivo de analisar qualitativa e quantitativamente a microbiota presente no líquido de estase esofágico de pacientes portadores de megaesôfago chagásico, comparando-a com a existente em indivíduos sadios. Foram estudados prospectivamente 25 pacientes (10 homens e 15 mulheres) com idades variando de 24 a 74 anos (  = 49,1a). Quinze pacientes eram portadores de esofagopatia chagásica, sendo 5 portadores de mega grau I (MG1), 5 portadores de mega grau II (MG2) e 5 portadores de mega grau III (MG3), segundo a classificação de Rezende; e 10 indivíduos sadios, agrupados no Grupo Controle (GC). Utilizou-se método de coleta que permitia aspiração de líquido através de sonda de Levine diretamente da luz esofágica, evitando-se a contaminação com microrganismos da orofaringe. Após análise microbiológica qualitativa e quantitativa, foi feita a descrição dos microrganismos encontrados nos vários grupos e sua classificação em aeróbios Gram positivos, aeróbios Gram negativos, anaeróbios e fungos. A análise estatística visou avaliar diferenças quantitativas entre os microrganismos nos diferentes grupos, sendo para tanto utilizado o teste não paramétrico de Kruskal-Wallis, com nível de rejeição menor 0,05 (5%). A positividade das culturas no Grupo Controle foi 40%, com predomínio do gênero Streptococcus sp, em concentrações que variaram de 101 a 102 ufc/ml. No Grupo Megaesôfago 93,3% da culturas foram positivas, com grande variedade de bactérias, mas predomínio de aeróbios Gram positivos (Streptococcus sp. foi o mais comum) e anaeróbios (Veillonella sp foi a mais freqüente) em concentrações que variaram de 101 a 105 ufc/ml. As concentrações foram geralmente mais elevadas em MG3, quando comparado com MG1, MG2 e GC (p<0,05). Concluiu-se que no megoesôfago, diferentemente dos indivíduos sadios, existe a presença de rica microflora bacteriana, constituída principalmente por aeróbios Gram positivos e anaeróbios, em concentrações tanto maiores quanto maior o seu grau de dilatação. Parte desta microbiota tem capacidade de metabolizar nitratos, etapa importante na formação de nitrosaminas.
Title in English
Microbiota in chagasic megaesophagus
Keywords in English
Achalasia
Chagas disease/ethiology
Esophageal achalasia/microbiology
Megaesophagus
Microbiology
Nitrate reductases/analysis
Nitroso compounds/analysis
Abstract in English
The stasis of saliva and swallowed food in the esophageal lumen of patients with chagasic megaesophagus causes: (1) bacterial overgrowth in the esophageal lumen, (2) recurring pulmonary aspirations and respiratory infections, (3) increased risk of surgical or endoscopic procedures if perforation occurs by the major possibility of contamination, and (4) the development of chronic inflammatory process in esophageal mucosa, that can predispose to the development of dysplasia and cancer. In spite of this, esophageal microbiota in the megaesophagus has never been studied. The aim of this study was to analyze qualitatively and quantitatively the microbiota in chagasic megaesophagus in comparison to the normal esophagus. Twenty-five patients (10 men and 15 women) were prospectively studied, with ages varying from 24 to 74 years (=49,1), from March to September 2000. Fifteen patients with chagasic megaesophagus (MG), were divided into three sub- groups according to the grade of esophageal dilation: MG1 – 5 patients with megaesophagus grade I; MG2- 5 patients with megaesophagus grade II; MG3- 5 patients with megaesophagus grade III. Another group of ten patients without any esophageal disease was constituted in the Control Group (CG). The sample collection was performed using a method specially developed to avoid contamination with microorganisms of the oral cavity and oropharynx. After qualitative and quantitative analysis, the microorganisms found were described and classified as Gram positive aerobes, Gram negative aerobes, anaerobes and fungus. Statistical analysis using Kruskal-Wallis non-parametric test was performed in order to find quantitative differences of microorganisms in the different groups. In CG 40% of the cultures were positive with predominance of the genus Streptococcus sp, in concentrations that varied from 101 to 102 cfu/ml. In MG, 93,3% of the cultures were positive, with great bacterial variability and predominance of a variety of aerobic Gram-positive (Streptococcus sp was the most common) and anaerobic bacteria (Veillonella sp was the most frequent), in concentrations that varied from 101 to 105 cfu/ml. The bacterial concentrations were generally more elevated in MG3 in comparison to MG1, MG2 and CG (p<0,05). It was concluded that patients with megaesophagus present a varied microbiota constituted mostly of aerobic Gram positive and anaerobic bacteria, in concentrations that vary with the megaesophagus dilatation degree. Some of the bacteria found in MG are able to metabolize nitrates intro nitrites, an important step in the formation of nitrosamines.
 
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Publishing Date
2006-05-16
 
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