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1.
J Periodontal Res ; 53(5): 721-726, 2018 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29687449

RESUMO

OBJECTIVE: The aim of the current study was to assess the association between 3 different calcium channel blockers (CCBs) (nifedipine, amlodipine and felodipine) and gingival overgrowth in patients with a diagnosis of severe refractory hypertension. METHODS: One hundred and sixty-two patients with severe refractory hypertension, taking CCBs, were selected. Gingival overgrowth was graded and periodontal measurements were recorded (probing pocket depth, clinical attachment level, plaque index and bleeding on probing). Unconditional multivariable binary logistic regression analyses were performed to assess the association between CCB intake and gingival overgrowth after adjusting for potential confounders. RESULTS: Of the 162 patients, 26 (16.0%) were current smokers and 101 (62.3%) were females. The mean age (SD) was 54.1 (8.5) years and the median age (range) 52.5 (39-78) years. Gingival overgrowth was observed in 55 patients (34.0%). Nifedipine was the most common medication (35.2%; 57 of 162). The results of multiple binary logistic regression showed statistically significant associations between CCB intake (exposure) and gingival overgrowth (outcome) after adjusting for the variables treatment time with antihypertensive and plaque index. Patients with gingival overgrowth were 2.5 (odds ratio = 2.46; 95% confidence interval: 1.04-5.82) and 4.0 (odds ratio = 3.90; 95% confidence interval: 1.47-10.35) times more likely to be taking nifedipine and amlodipine, respectively, than patients without gingival overgrowth. On the other hand, this significant association was not observed for felodipine. CONCLUSION: Nifedipine and amlodipine, but not felodipine, were associated with gingival overgrowth in patients with severe refractory hypertension.


Assuntos
Bloqueadores dos Canais de Cálcio/efeitos adversos , Crescimento Excessivo da Gengiva/induzido quimicamente , Hipertensão/tratamento farmacológico , Adulto , Idoso , Anlodipino/efeitos adversos , Brasil , Felodipino/efeitos adversos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Nifedipino/efeitos adversos , Índice Periodontal
2.
J Periodontal Res ; 51(1): 95-102, 2016 02.
Artigo em Inglês | MEDLINE | ID: mdl-26040412

RESUMO

BACKGROUND AND OBJECTIVE: To compare the subgingival microbial diversity between non-HIV-infected and HIV-infected individuals with chronic periodontitis using denaturing gradient gel electrophoresis (DGGE). MATERIAL AND METHODS: Thirty-two patients were selected: 11 were HIV-infected and 21 were non-HIV-infected, and all had chronic periodontitis. Periodontal measurements included probing depth, clinical attachment level, visible supragingival biofilm and bleeding on probing. Subgingival biofilm samples were collected from periodontal sites (50% with probing depth ≤ 4 mm and 50% with probing depth ≥ 5 mm) and whole-genomic-amplified DNA was obtained. The DNA samples were subjected to amplification of a 16S rRNA gene fragment using universal bacterial primers, followed by DGGE analysis of the amplified gene sequences. RESULTS: The non-HIV-infected group presented higher mean full-mouth visible supragingival biofilm (p = 0.004), bleeding on probing (p = 0.006), probing depth (p < 0.001) and clinical attachment level (p = 0.001) in comparison with the HIV-infected group. DGGE analysis revealed 81 distinct bands from all 33 individuals. Banding profiles revealed a higher diversity of the bacterial communities in the subgingival biofilm of HIV-infected patients with chronic periodontitis. Moreover, cluster and principal component analyses demonstrated that the bacterial community profiles differed between these two conditions. High interindividual and intra-individual variability in banding profiles were observed for both groups. CONCLUSION: HIV-infected patients with chronic periodontitis present greater subgingival microbial diversity. In addition, the bacterial communities associated with HIV-infected and non-HIV-infected individuals are different in structure.


Assuntos
Periodontite Crônica , Adulto , Brasil , DNA Bacteriano , Placa Dentária , Infecções por HIV , Humanos , Bolsa Periodontal , RNA Ribossômico 16S
3.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;48(7): 588-594, 07/2015. tab
Artigo em Inglês | LILACS | ID: lil-751349

RESUMO

Staphylococcus aureus is highly prevalent among patients with atopic dermatitis (AD), and this pathogen may trigger and aggravate AD lesions. The aim of this study was to determine the prevalence of S. aureus in the nares of pediatric subjects and verify the phenotypic and molecular characteristics of the isolates in pediatric patients with AD. Isolates were tested for antimicrobial susceptibility, SCCmec typing, and Panton-Valentine Leukocidin (PVL) genes. Lineages were determined by pulsed-field gel electrophoresis and multilocus sequence typing (MLST). AD severity was assessed with the Scoring Atopic Dermatitis (SCORAD) index. Among 106 patients, 90 (85%) presented S. aureus isolates in their nares, and 8 also presented the pathogen in their skin infections. Two patients had two positive lesions, making a total of 10 S. aureus isolates from skin infections. Methicillin-resistant S. aureus (MRSA) was detected in 24 (26.6%) patients, and PVL genes were identified in 21 (23.3%), including 6 (75%) of the 8 patients with skin lesions but mainly in patients with severe and moderate SCORAD values (P=0.0095). All 24 MRSA isolates were susceptible to trimethoprim/sulfamethoxazole, while 8 isolates had a minimum inhibitory concentration (MIC) to mupirocin >1024 μg/mL. High lineage diversity was found among the isolates including USA1100/ST30, USA400/ST1, USA800/ST5, ST83, ST188, ST718, ST1635, and ST2791. There was a high prevalence of MRSA and PVL genes among the isolates recovered in this study. PVL genes were found mostly among patients with severe and moderate SCORAD values. These findings can help clinicians improve the therapies and strategies for the management of pediatric patients with AD.


Assuntos
Animais , Masculino , Camundongos , Ratos , Nefropatias/metabolismo , Rim/metabolismo , Podócitos/metabolismo , Transdução de Sinais , Células Cultivadas , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/metabolismo , Proteínas Quinases Dependentes de AMP Cíclico/metabolismo , Expressão Gênica , Redes Reguladoras de Genes , Immunoblotting , Nefropatias/induzido quimicamente , Nefropatias/genética , Rim/patologia , Rim/fisiopatologia , Microscopia Eletrônica , Proteínas de Membrana/genética , Proteínas de Membrana/metabolismo , Proteínas dos Microfilamentos/genética , Proteínas dos Microfilamentos/metabolismo , Puromicina , Podócitos/patologia , Podócitos/ultraestrutura , Proteômica/métodos , Ratos Sprague-Dawley , Reação em Cadeia da Polimerase Via Transcriptase Reversa
4.
Braz J Med Biol Res ; 48(7): 588-94, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25992644

RESUMO

Staphylococcus aureus is highly prevalent among patients with atopic dermatitis (AD), and this pathogen may trigger and aggravate AD lesions. The aim of this study was to determine the prevalence of S. aureus in the nares of pediatric subjects and verify the phenotypic and molecular characteristics of the isolates in pediatric patients with AD. Isolates were tested for antimicrobial susceptibility, SCCmec typing, and Panton-Valentine Leukocidin (PVL) genes. Lineages were determined by pulsed-field gel electrophoresis and multilocus sequence typing (MLST). AD severity was assessed with the Scoring Atopic Dermatitis (SCORAD) index. Among 106 patients, 90 (85%) presented S. aureus isolates in their nares, and 8 also presented the pathogen in their skin infections. Two patients had two positive lesions, making a total of 10 S. aureus isolates from skin infections. Methicillin-resistant S. aureus (MRSA) was detected in 24 (26.6%) patients, and PVL genes were identified in 21 (23.3%), including 6 (75%) of the 8 patients with skin lesions but mainly in patients with severe and moderate SCORAD values (P=0.0095). All 24 MRSA isolates were susceptible to trimethoprim/sulfamethoxazole, while 8 isolates had a minimum inhibitory concentration (MIC) to mupirocin >1024 µg/mL. High lineage diversity was found among the isolates including USA1100/ST30, USA400/ST1, USA800/ST5, ST83, ST188, ST718, ST1635, and ST2791. There was a high prevalence of MRSA and PVL genes among the isolates recovered in this study. PVL genes were found mostly among patients with severe and moderate SCORAD values. These findings can help clinicians improve the therapies and strategies for the management of pediatric patients with AD.


Assuntos
Toxinas Bacterianas/genética , Dermatite Atópica/microbiologia , Exotoxinas/genética , Leucocidinas/genética , Staphylococcus aureus Resistente à Meticilina/genética , Cavidade Nasal/microbiologia , Pele/microbiologia , Adolescente , Criança , Estudos Transversais , DNA Bacteriano , Eletroforese em Gel de Campo Pulsado , Feminino , Humanos , Masculino , Testes de Sensibilidade Microbiana , Tipagem de Sequências Multilocus , Reação em Cadeia da Polimerase , Valores de Referência , Índice de Gravidade de Doença , Infecções Cutâneas Estafilocócicas/microbiologia
5.
J Appl Microbiol ; 116(6): 1418-26, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24524649

RESUMO

AIM: To evaluate the synergistic activity of antimicrobial drugs against lineages of methicillin-resistant Staphylococcus aureus (MRSA) carrying SCCmec IV. The biofilm production and related genes were also detected. METHODS AND RESULTS: Forty two MRSA isolates were tested for biofilm production and related genes. Biofilm/biomass susceptibility to gentamicin (G), linezolid (L), rifampicin (R) and vancomycin (V) was determined for six isolates from three lineages prevalent in Rio de Janeiro hospitals in concentrations ranging from 0·25 to 64 µg ml(-1). Biomass was evaluated by microtitre plate test and number of viable cells (CFU cm(-2)) and inspected by epifluorescence microscopy. All isolates presented the icaA and sasG genes, but only 38% were biofilm producers. There were 50 and 45% biomass reductions when concentrations ≥4 µg ml(-1) of R or L and ≥16 µg ml(-1) of G or V, respectively, were used. Synergism tests produced a 55% biomass reduction with R(2µgml-1) + G(16µgml-1), R(2µgml-1) + L(2µgml-1), R(2µgml-1) + V(4µgml-1), and L(2µgml-1) + V(4µgml-1). Number of viable cells was reduced from 2 to 3 logs with R(2µgml-1) + L(2µgml-1) and R(2µgml-1) + V(4µgml-1). CONCLUSIONS: Synergisms involving R plus L and R plus V caused important reductions in biofilm/biomass and the number of viable cells. Drug combinations should be considered in the chemotherapies of MRSA-SCCmec IV infections. SIGNIFICANCE AND IMPACT OF THE STUDY: Biofilms in MRSA infections restrict the clinical choice of antimicrobials. Thus, knowledge of the best options for monotherapy and drug synergisms could improve clinical results.


Assuntos
Antibacterianos/farmacologia , Staphylococcus aureus Resistente à Meticilina/efeitos dos fármacos , Acetamidas/farmacologia , Biofilmes/efeitos dos fármacos , Biomassa , Sinergismo Farmacológico , Gentamicinas/farmacologia , Humanos , Linezolida , Staphylococcus aureus Resistente à Meticilina/genética , Testes de Sensibilidade Microbiana , Viabilidade Microbiana , Oxazolidinonas/farmacologia , Rifampina/farmacologia , Vancomicina/farmacologia
6.
J Hosp Infect ; 86(2): 151-4, 2014 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24433925

RESUMO

This study aimed to characterize meticillin-resistant Staphylococcus aureus (MRSA) lineages circulating in a Brazilian teaching hospital. MRSA isolates from nasal swabs were evaluated to assess antimicrobial susceptibility, staphylococcal cassette chromosome mec (SCCmec), Panton-Valentine leucocidin status, pulsed-field gel electrophoresis profile and multi-locus sequence type (MLST) analysis. Eighty-three MRSA isolates were analysed. SCCmec III (43.4%) and IV (49.4%) were predominant. ST1-IV (USA400) was more common in internal medicine (P = 0.002) whereas 'clone M' (SCCmec III) was more common in the medical and surgical intensive care unit (P = 0.004), and all isolates were ST5-IV (USA800) in dermatology (P < 0.001). These data improved the understanding of the MRSA epidemiology inside the hospital and helped to establish effective control measures.


Assuntos
Portador Sadio/epidemiologia , Infecção Hospitalar/epidemiologia , Staphylococcus aureus Resistente à Meticilina/isolamento & purificação , Infecções Estafilocócicas/epidemiologia , Brasil/epidemiologia , Portador Sadio/microbiologia , Infecção Hospitalar/microbiologia , Genes Bacterianos , Genótipo , Hospitais de Ensino , Humanos , Testes de Sensibilidade Microbiana , Epidemiologia Molecular , Tipagem Molecular , Mucosa Nasal/microbiologia , Infecções Estafilocócicas/microbiologia , Fatores de Virulência/genética
8.
São Paulo; SMS; set. 2013. 175 p.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940601
9.
São Paulo; SMS; set. 2013.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940211
10.
São Paulo; SMS; set. 2013.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940213
11.
São Paulo; SMS; set. 2013.
Monografia em Português | Sec. Munic. Saúde SP, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: sms-8917
12.
São Paulo; SMS; set. 2013.
Monografia em Português | Sec. Munic. Saúde SP, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: sms-8919
13.
São Paulo; SMS; set. 2013. 175 p.
Monografia em Português | Sec. Munic. Saúde SP, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: sms-8989
15.
Int Endod J ; 46(3): 225-33, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22889410

RESUMO

AIM: To evaluate clinically the antibacterial effects of root canal treatment procedures using molecular microbiology analyses. METHODOLOGY: Samples were taken from 14 necrotic root canals of teeth with apical periodontitis before (S1) and after instrumentation with NaOCl irrigation (S2), a final rinse with chlorhexidine (CHX) (S3) and then one-week interappointment medication with calcium hydroxide/CHX paste (S4). The parameters examined included the following: incidence of positive broad-range PCR results for bacterial presence; impact on bacterial community structures evaluated by PCR-Denaturing Gradient Gel Electrophoresis (DGGE); quantitative bacterial reduction determined by real-time PCR; and identification of bacterial persisters by cloning and sequencing. Data from the different tests were subjected to statistical analyses and diversity indicator calculations. RESULTS: All S1 samples were positive for bacteria in all tests. Treatment procedures promoted a decrease in microbial diversity and significantly reduced the incidence of positive results and the bacterial counts (P < 0.05). In general, each subsequent treatment step improved disinfection. No specific taxon or community pattern was associated with post-treatment samples. CONCLUSION: Supplementary steps consisting of a final rinse with CHX followed by calcium hydroxide interappointment medication promoted further decrease in the bacterial bioburden to levels significantly below those achieved by the chemomechanical procedures alone. Because the long-term outcome of root canal treatment is dependent upon maximal bacterial reduction, the present results are of clinical relevance.


Assuntos
Anti-Infecciosos Locais/uso terapêutico , Hidróxido de Cálcio/uso terapêutico , Clorexidina/análogos & derivados , Ligas Dentárias , Desinfecção/métodos , Níquel , Irrigantes do Canal Radicular/uso terapêutico , Preparo de Canal Radicular/instrumentação , Hipoclorito de Sódio/uso terapêutico , Titânio , Carga Bacteriana/efeitos dos fármacos , Biodiversidade , Clorexidina/uso terapêutico , Eletroforese em Gel de Gradiente Desnaturante , Ligas Dentárias/química , Polpa Dentária/microbiologia , Cavidade Pulpar/microbiologia , Necrose da Polpa Dentária/microbiologia , Necrose da Polpa Dentária/terapia , Ácido Edético/uso terapêutico , Bactérias Gram-Negativas/classificação , Bactérias Gram-Negativas/genética , Bactérias Gram-Positivas/classificação , Bactérias Gram-Positivas/genética , Humanos , Consórcios Microbianos/efeitos dos fármacos , Biologia Molecular , Níquel/química , Periodontite Periapical/microbiologia , Periodontite Periapical/terapia , RNA Bacteriano/análise , RNA Ribossômico 16S/análise , Reação em Cadeia da Polimerase em Tempo Real , Preparo de Canal Radicular/métodos , Análise de Sequência de RNA , Camada de Esfregaço , Titânio/química
16.
São Paulo; SMS; 2012. 242 p.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940708
17.
São Paulo; SMS; 2012.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940709
18.
São Paulo; SMS; 2012. 169 p.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940714
19.
São Paulo; SMS; 2012. 167 p.
Monografia em Português | Coleciona SUS, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: biblio-940716
20.
São Paulo; SMS; 2012.
Monografia em Português | Sec. Munic. Saúde SP, CACHOEIRINHA-Producao, Sec. Munic. Saúde SP, Sec. Munic. Saúde SP | ID: sms-9379
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