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1.
Rev Invest Clin ; 71(3): 204-210, 2019.
Article in English | MEDLINE | ID: mdl-31184336

ABSTRACT

BACKGROUND: Osteoporosis (OP) is common in patients with chronic obstructive pulmonary disease (COPD). The relationship between OP and COPD has been primarily studied in male patients, and few reports are available in postmenopausal women. OBJECTIVE: The purpose of this study was to investigate the association between bone mineral density (BMD) and COPD in postmenopausal women. METHODS: This cross-sectional study included 133 clinically stable female ex-smokers with confirmed COPD, and 31 age-matched "ex-smoker" female controls. We analyzed groups according to their airway obstruction category. BMD was measured on dual-energy X-ray absorptiometry images of the left femoral neck. RESULTS: Patients with COPD had lower T-scores and higher prevalence of osteopenia/OP than the control group. In the COPD group, the airway obstruction category was significantly associated with the T-score after adjustment for confounders. Multivariate logistic regression analysis showed COPD was an independent marker for increased risk of osteopenia/OP in postmenopausal women. CONCLUSIONS: COPD and airway obstruction category were strongly related to BMD. Postmenopausal women with COPD, especially those with severe airway obstruction, had a higher prevalence rate and a higher risk of osteopenia and OP than female controls without COPD.


Subject(s)
Bone Density/physiology , Osteoporosis, Postmenopausal/epidemiology , Postmenopause , Pulmonary Disease, Chronic Obstructive/complications , Absorptiometry, Photon , Aged , Airway Obstruction/etiology , Airway Obstruction/physiopathology , Bone Diseases, Metabolic/epidemiology , Case-Control Studies , Cross-Sectional Studies , Female , Humans , Middle Aged , Prevalence , Pulmonary Disease, Chronic Obstructive/physiopathology , Risk Factors
2.
Rev. invest. clín ; Rev. invest. clín;71(3): 204-210, May.-Jun. 2019. tab, graf
Article in English | LILACS | ID: biblio-1289688

ABSTRACT

Abstract Background Osteoporosis (OP) is common in patients with chronic obstructive pulmonary disease (COPD). The relationship between OP and COPD has been primarily studied in male patients, and few reports are available in postmenopausal women. Objective The purpose of this study was to investigate the association between bone mineral density (BMD) and COPD in postmenopausal women. Methods This cross-sectional study included 133 clinically stable female ex-smokers with confirmed COPD, and 31 age-matched “ex-smoker” female controls. We analyzed groups according to their airway obstruction category. BMD was measured on dual-energy X-ray absorptiometry images of the left femoral neck. Results Patients with COPD had lower T-scores and higher prevalence of osteopenia/OP than the control group. In the COPD group, the airway obstruction category was significantly associated with the T-score after adjustment for confounders. Multivariate logistic regression analysis showed COPD was an independent marker for increased risk of osteopenia/OP in postmenopausal women. Conclusions COPD and airway obstruction category were strongly related to BMD. Postmenopausal women with COPD, especially those with severe airway obstruction, had a higher prevalence rate and a higher risk of osteopenia and OP than female controls without COPD.


Subject(s)
Humans , Female , Middle Aged , Aged , Bone Density/physiology , Osteoporosis, Postmenopausal/epidemiology , Postmenopause , Pulmonary Disease, Chronic Obstructive/complications , Bone Diseases, Metabolic/epidemiology , Absorptiometry, Photon , Case-Control Studies , Prevalence , Cross-Sectional Studies , Risk Factors , Pulmonary Disease, Chronic Obstructive/physiopathology , Airway Obstruction/etiology , Airway Obstruction/physiopathology
3.
J Appl Oral Sci ; 26: e20170113, 2018.
Article in English | MEDLINE | ID: mdl-29489935

ABSTRACT

Dental caries is a chronic progressive disease occurring in the tooth hard tissue due to multiple factors, in which bacteria are the initial cause. Both Streptococcus mutans and Streptococcus sanguinis are main members of oral biofilm. Helicobacter pylori may also be detected in dental plaque, playing an important role in the development of dental caries. OBJECTIVE: The aim of this study was to investigate the effect of H. pylori culture supernatant on S. mutans and S. sanguinis dual-species biofilm and to evaluate its potential ability on affecting dental health. MATERIAL AND METHODS: The effect of H. pylori supernatant on single-species and dual-species biofilm was measured by colony forming units counting and fluorescence in situ hybridization (FISH) assay, respectively. The effect of H. pylori supernatant on S. mutans and S. sanguinis extracellular polysaccharides (EPS) production was measured by both confocal laser scanning microscopy observation and anthrone-sulfuric acid method. The effect of H. pylori supernatant on S. mutans gene expression was measured by quantitative real-time PCR (qRT-PCR) assays. RESULTS: H. pylori supernatant could inhibit both S. mutans and S. sanguinis biofilm formation and EPS production. S. sanguinis inhibition rate was significantly higher than that of S. mutans. Finally, S. mutans bacteriocin and acidogenicity related genes expression were affected by H. pylori culture supernatant. CONCLUSION: Our results showed that H. pylori could destroy the balance between S. mutans and S. sanguinis in oral biofilm, creating an advantageous environment for S. mutans, which became the dominant bacteria, promoting the formation and development of dental caries.


Subject(s)
Biofilms , Dental Plaque/microbiology , Helicobacter pylori/physiology , Streptococcus mutans/physiology , Streptococcus sanguis/physiology , Colony Count, Microbial , Dental Caries/microbiology , Gene Expression , Helicobacter pylori/genetics , In Situ Hybridization, Fluorescence , Microscopy, Confocal , Plankton/growth & development , Polysaccharides, Bacterial/metabolism , Real-Time Polymerase Chain Reaction , Streptococcus mutans/genetics , Streptococcus sanguis/genetics , Time Factors
4.
J. appl. oral sci ; J. appl. oral sci;26: e20170113, 2018. graf
Article in English | LILACS, BBO - Dentistry | ID: biblio-893693

ABSTRACT

Abstract Dental caries is a chronic progressive disease occurring in the tooth hard tissue due to multiple factors, in which bacteria are the initial cause. Both Streptococcus mutans and Streptococcus sanguinis are main members of oral biofilm. Helicobacter pylori may also be detected in dental plaque, playing an important role in the development of dental caries. Objective The aim of this study was to investigate the effect of H. pylori culture supernatant on S. mutans and S. sanguinis dual-species biofilm and to evaluate its potential ability on affecting dental health. Material and methods The effect of H. pylori supernatant on single-species and dual-species biofilm was measured by colony forming units counting and fluorescence in situ hybridization (FISH) assay, respectively. The effect of H. pylori supernatant on S. mutans and S. sanguinis extracellular polysaccharides (EPS) production was measured by both confocal laser scanning microscopy observation and anthrone-sulfuric acid method. The effect of H. pylori supernatant on S. mutans gene expression was measured by quantitative real-time PCR (qRT-PCR) assays. Results H. pylori supernatant could inhibit both S. mutans and S. sanguinis biofilm formation and EPS production. S. sanguinis inhibition rate was significantly higher than that of S. mutans. Finally, S. mutans bacteriocin and acidogenicity related genes expression were affected by H. pylori culture supernatant. Conclusion Our results showed that H. pylori could destroy the balance between S. mutans and S. sanguinis in oral biofilm, creating an advantageous environment for S. mutans, which became the dominant bacteria, promoting the formation and development of dental caries.


Subject(s)
Streptococcus mutans/physiology , Streptococcus sanguis/physiology , Helicobacter pylori/physiology , Biofilms , Dental Plaque/microbiology , Plankton/growth & development , Polysaccharides, Bacterial/metabolism , Streptococcus mutans/genetics , Streptococcus sanguis/genetics , Time Factors , Colony Count, Microbial , Gene Expression , Helicobacter pylori/genetics , In Situ Hybridization, Fluorescence , Microscopy, Confocal , Dental Caries/microbiology , Real-Time Polymerase Chain Reaction
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