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1.
Int J Tuberc Lung Dis ; 18(8): 995-7, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25199019

RESUMO

An association has been suggested between Marfan syndrome (MFS) and the nodular bronchiectatic form of lung disease caused by non-tuberculous mycobacteria (NTM). We evaluated the prevalence of bronchiectasis in 79 adult patients with MFS using computed tomography (CT) imaging. Airway dilation indicative of bronchiectasis (22/79, 28%) and bronchioloectasis (10/79, 13%) were relatively common, although the extent of dilation was not severe and was frequently confined to a single lobe. However, bronchiolitis was evident in only three patients (4%), and no patient was diagnosed with NTM lung disease.


Assuntos
Bronquiectasia/epidemiologia , Síndrome de Marfan/complicações , Infecções por Mycobacterium não Tuberculosas/epidemiologia , Micobactérias não Tuberculosas/isolamento & purificação , Adulto , Bronquiectasia/microbiologia , Bronquiolite/epidemiologia , Bronquiolite/microbiologia , Feminino , Humanos , Masculino , Síndrome de Marfan/microbiologia , Pessoa de Meia-Idade , Infecções por Mycobacterium não Tuberculosas/microbiologia , Prevalência , Estudos Retrospectivos , Tomografia Computadorizada por Raios X
2.
Infect Immun ; 81(1): 182-8, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23115041

RESUMO

Marfan syndrome is an autosomal dominant disease characterized by aneurysm and dilatation of the aortic root, tall stature, and ectopia lentis. These manifestations reflect excessive signaling of transforming growth factor beta (TGF-ß). Moreover, cases are frequently associated with severe periodontitis, which is a chronic inflammation of the gingiva, periodontal ligament, and alveolar bone. Recently, angiotensin II receptor blockers (ARBs) were discovered to be an effective drug class that can prevent aortic aneurysm and dilation in Marfan syndrome by inhibiting TGF-ß signaling. To investigate the effect of ARB on the progression of periodontitis, the application of a potent ARB, telmisartan, was examined in a mouse model of Marfan syndrome (MgΔ). Six-week-old male heterozygous MgΔ and wild-type mice were challenged with Porphyromonas gingivalis, which causes chronic periodontitis, with and without telmisartan application. After infection, alveolar bone resorption was measured by micro-computed tomography (µCT), and inflammatory cytokine levels were examined. Infection of Porphyromonas gingivalis induced alveolar bone resorption in both MgΔ and wild-type mice. The amount of resorption was significantly larger in the former than the latter. Immunoarray and enzyme-linked immunosorbent assay (ELISA) analyses demonstrated that interleukin-17 (IL-17) and tumor necrosis factor alpha (TNF-α) levels were significantly higher in infected MgΔ mice than infected wild-type mice. Telmisartan treatment significantly suppressed the alveolar bone resorption of infected MgΔ mice. Telmisartan also significantly decreased levels of TGF-ß, IL-17, and TNF-α in infected MgΔ mice to levels seen in infected wild-type mice. This study suggests that ARB can prevent the severe periodontitis frequently seen in Marfan syndrome.


Assuntos
Antagonistas de Receptores de Angiotensina/farmacologia , Síndrome de Marfan/tratamento farmacológico , Periodontite/tratamento farmacológico , Perda do Osso Alveolar/tratamento farmacológico , Perda do Osso Alveolar/metabolismo , Perda do Osso Alveolar/microbiologia , Animais , Infecções por Bacteroidaceae/tratamento farmacológico , Infecções por Bacteroidaceae/metabolismo , Infecções por Bacteroidaceae/microbiologia , Benzimidazóis/farmacologia , Benzoatos/farmacologia , Reabsorção Óssea/tratamento farmacológico , Reabsorção Óssea/metabolismo , Reabsorção Óssea/microbiologia , Modelos Animais de Doenças , Inflamação/tratamento farmacológico , Inflamação/metabolismo , Inflamação/microbiologia , Interleucina-17/metabolismo , Masculino , Síndrome de Marfan/metabolismo , Síndrome de Marfan/microbiologia , Camundongos , Osteoclastos/efeitos dos fármacos , Osteoclastos/metabolismo , Periodontite/metabolismo , Periodontite/microbiologia , Porphyromonas gingivalis/metabolismo , Telmisartan , Fator de Crescimento Transformador beta/metabolismo , Fator de Necrose Tumoral alfa/metabolismo
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