Dentin hipersensitivity following non-surgical periodontal therapy with hand or ultrasonic instruments / Hipersensibilidade dentinária após terapia periodontal não cirúrgica com instrumentos manuais ou ultrassônicos

Periodontal instrumentation aims to remove plaque and calculus from the root surface. Both manual and ultrasonic instruments have been used for such decontamination; however, establishing a healthy periodontium can result in adverse effects, such as dentin hypersensitivity. Objective: To evaluate the effects of hand or ultrasonic instrumentation on dentin hypersensitivity in patients undergoing non-surgical periodontal treatment. For this controlled clinical trial of a "split mouth" design, 14 patients were selected with homologous teeth in the incisor to premolar region and probing depth ≥ 5 mm on the buccal aspect of the teeth. One side (control) was instrumented with hand instruments and the other side (test) with ultrasonic instruments. Dentin hypersensitivity was assessed on baseline and during the 4 weeks after treatment, with a periodontal probe scratching the root surface and with an air jet. The patient's response was detected by a visual analog scale of 10 cm. There was no statistical difference between the effectiveness and the occurrence of hypersensitivity between the proposed therapies. After the instrumentation the occurrence of hypersensitivity occurred at low levels, and disappeared completely at 4 weeks of evaluation. In the first week, there was a statistically significant increase in hypersensitivity in the control group after stimulation with air. The air jet stimulus, in comparison to scratching caused more discomfort during the hypersensitivity evaluation after the both treatments on the 1st, 2nd and 3rd weeks. Based on these conditions, this study demonstrated that there was no difference in dentin hypersensitivity following ultrasonic or hand instrumentation (AU)

A instrumentação periodontal tem como objetivo remover biofilme e cálculo dental da superfície radicular. Tanto instrumentos manuais quanto ultrassônicos já foram consolidados como capazes de promover essa descontaminação. Contudo, o estabelecimento de um periodonto saudável pode resultar em efeitos adversos como a hipersensibilidade dentinária. O objetivo do presente estudo foi avaliar os efeitos da instrumentação manual ou ultrassônica sobre a hipersensibilidade dentinária em pacientes submetidos ao tratamento periodontal não-cirúrgico. Para realização deste estudo clínico controlado de "boca dividida" foram selecionados 14 pacientes com dentes homólogos na região de incisivos a pré-molares com profundidade de sondagem ≥ 5 mm, na face vestibular. Um lado (controle) recebeu instrumentação com curetas e o outro (teste) instrumentação ultrassônica. A hipersensibilidade dentinária foi avaliada, antes e durante 4 semanas após o tratamento, com uma sonda periodontal arranhando a superfície radicular e com um jato de ar. A resposta do paciente foi detectada por meio de uma Escala Visual Analógica (EVA) de 10 cm. Não houve diferença estatística entre a efetividade e a ocorrência de hipersensibilidade das terapias propostas. Após as instrumentações a ocorrência da sensibilidade ocorreu em níveis leves, e desapareceu completamente na 4ª semana de avaliação. Na primeira semana houve aumento da hipersensibilidade estatisticamente significante apenas no grupo controle após estímulo com ar. O estímulo do jato de ar em comparação ao estímulo da ranhura causou maior desconforto na avaliação da hipersensibilidade após o tratamento com curetas ou pontas ultrassônicas na 1ª, 2ª e 3ª semanas. Dentro dessas condições, este estudo demontrou que não ocorreu diferença da hipersensibilidade dentinária produzida pela instrumentação manual e ultrassônica. (AU)

Obesity and dyslipidemia in patients with psoriasis treated at a dermatologic clinic in Manaus / Obesidade e dislipidemia em pacientes com psoriase atendidos num ambulatorio de dermatologia de Manaus

BACKGROUND: Psoriasis is a chronic inflammatory disease of multifactorial etiology, with participation of genetic, autoimmune and environmental factors. Recent studies have demonstrated the role of inflammatory cells and mediators in the pathogenesis of psoriasis, which is now defined as a systemic and autoimmune inflammatory disease that may be associated with other diseases of inflammatory nature. OBJECTIVES: To evaluate the occurrence of obesity and dyslipidemia in patients with psoriasis treated at a dermatology clinic in Manaus. METHODS: We performed a prospective descriptive study to assess the prevalence of obesity and dyslipidemia in patients with psoriasis. Besides the recommended dermatological care, a physical examination was performed to measure weight, height and waist circumference. RESULTS: We included 72 patients, 44 (61.1%) female and 28 (38.9%) male, with a mean age of 51.0 years ± 15.9 years. As for body mass index (BMI), 16 (22.2%) were overweight and 20 (27.8%) were obese. In the analysis of waist circumference in relation to gender, we found that 79.5% of women surveyed had central obesity, a percentage statistically higher than that observed among men (42.9%) at the 5% level of significance (p = 0.001). Regarding the diagnosis of dyslipidemia, 29 (65.9%) females and 22 (78.6%) males showed alterations in lipid profile. CONCLUSIONS: The occurrence of dyslipidemia and obesity in patients with psoriasis can affect life quality and expectancy, increasing the risk of systemic and metabolic diseases, which makes periodic investigation of these comorbidities in patients with psoriasis mandatory. .

FUNDAMENTOS: A psoríase é uma doença inflamatória crônica, com etiologia multifatorial, com participação de fatores genéticos, auto-imunes e ambientais. Estudos recentes demonstram o papel de células e mediadores inflamatórios na patogênese da psoríase, que passou a ser definida como uma afecção inflamatória sistêmica e auto-imune, podendo associarse a outras doenças de natureza inflamatória. OBJETIVOS: Avaliar a ocorrência de obesidade e dislipidemia em pacientes com psoríase atendidos num ambulatório de dermatologia de Manaus. MÉTODOS: Foi realizado estudo descritivo e prospectivo para avaliar a ocorrência de obesidade e dislipidemia em pacientes com psoríase. Além do atendimento dermatológico preconizado, foi realizado exame físico com medida de peso, altura e circunferência abdominal. RESULTADOS: Foram incluídos 72 pacientes, sendo 44 (61,1%) do sexo feminino e 28 (38,9%) do sexo masculino, com média de idade de 51,0 anos ± 15,9 anos. Quanto ao índice de massa corporal, 16 (22,2%) apresentavam sobrepeso e 20 (27,8%), obesidade. Na análise da circunferência abdominal em relação ao gênero, observou-se que 79,5% das mulheres examinadas apresentavam obesidade central, percentual estatisticamente maior que o observado entre os homens (42,9%), ao nível de 5% de significância (p= 0,001). Em relação ao diagnóstico de dislipidemia, 29 (65,9%) do sexo feminino e 22 (78,6%) do masculino apresentaram alteração no lipidograma. CONCLUSÕES: A ocorrência de dislipidemia e obesidade nos pacientes com psoríase pode alterar a qualidade e expectativa de vida, aumentando o risco de doenças sistêmicas e metabólicas, o que torna obrigatória a investigação periódica dessas ...

Sickle cell disease: acute clinical manifestations in early childhood and molecular characteristics in a group of children in Rio de Janeiro

OBJECTIVE: To describe clinical events of sickle cell disease and the correlation with β-globin haplotypes and α-thalassemia in under 6-year-old children. METHODS: A retrospective study was conducted of under 6-year-old children from the neonatal screening program in Rio de Janeiro. Forty-eight male and 48 female children were enrolled in this study, 79 with sickle cell anemia and 17 with hemoglobin SC. The mean age was 29.9 (standard deviation = 20.9) months, 62 (16.2 ± 8.6) were aged between 0-3 years old and 34 (54.9 ± 11.3) were from 3-6 years old. Painful events, acute splenic sequestration, hemolytic crises, hand-foot and acute chest syndromes and infections were evaluated. RESULTS: The events were more frequent in under 3-year-old children, 94% of children had at least one episode. Infection was the most common event affecting 88.5% of children. Acute splenic sequestration took place earlier, while painful crises and acute chest syndromes in under 6-year-old children. Thal-α 3.7 was observed in 20.9% of cases. Bantu was the most frequent haplotype found, followed by Benin. No correlation was observed between clinical events and β-globin haplotypes. Children with sickle cell anemia and α-thalassemia have less infectious events. No correlation was found among these polymorphisms and clinical events, however, the majority of children with Bantu/Bantu and without α-thalassemia had more clinical events.

Genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro, Brazil / Polimorfismos genéticos e doença cerebrovascular em crianças com anemia falciforme do Rio do Janeiro, Brasil

The aim of the present work was to examine possible genetic risk factors related to the occurrence of cerebrovascular disease (CVD) in Brazilian population, the frequency of βS-globin gene haplotypes and co-inheritance with α-thalassemia (-α3.7kb) and single nucleotide polymorphism of methylenetetrahydrofolate reductase (MTHFR-C677T), Factor V Leiden (FV-G1691A) and prothrombin (PT-G20210A) genes in children from Rio de Janeiro. Ninety four children with sickle cell anemia (SCA) were included, 24 patients with cerebrovascular involvement and 70 patients without CVD as control group. The mean age of children at the time of the cerebrovascular event was similar to the control group. The frequency of -α3.7kb thalassemia was similar in both groups (p=0.751). Children with Bantu/Atypical βS-globin gene haplotype presented 15 times more chance (OR=15.4 CI 95 percent 2.9-81.6) of CVD than the other βS-globin gene haplotypes. The C677T polymorphism of MTHFR gene was similar in both groups (p=0.085). No mutation in the FV Leiden or PT genes was found. A large study seems necessary to establish the role of these genetic polymorphisms in Brazilian miscegenated population.

Avaliar o papel da talassemia alfa (-α3.7kb), dos haplótipos da globina βS, e mutações nos genes da metileno-tetrahidrofolato redutase (MTHFR-C677T), fator V de Leiden (FV-G1691A) e protrombina (PT-G20210A) como fatores de risco para a doença cerebrovascular em pacientes com anemia falciforme. Foi realizado um estudo de caso controle com 94 crianças portadoras de anemia falciforme, 24 com doença cerebrovascular (DCV) e 70 sem DCV como grupo controle. A frequência de talassemia -α3.7kb foi semelhante em ambos os grupos (p=0,751). Crianças portadoras do haplótipo Bantu/Atípico da globina βS apresentam 15 vezes mais chances de desenvolverem DCV (OR=15,4 IC 95 por cento 2,9-81,6) do que os outros haplótipos. A frequência do polimorfismo MTHFR-C677T foi semelhante em ambos os grupos (p=0,085) e não foi observada mutação nos genes fator V e protrombina. Estudos com maior número de casos são necessários para esclarecer o papel desses polimorfismos genéticos na nossa população.

Bovine papillomavirus type 2 in reproductive tract and gametes of slaughtered bovine females

Os vírus do papiloma bovino, descritos como agentes infectantes específicos do epitélio, têm sido associados a diversas formas de câncer em diferentes espécies animais. Dada a intensa disseminação da papilomatose nos rebanhos, a investigação de diferentes formas de transmissão e seus respectivos mecanismos tem exigido especial atenção. No presente estudo, é relatada a detecção de seqüências genômicas do papilomavirus bovino (BPV) em ovócitos e tecidos do trato reprodutivo oriundos de fêmeas abatidas comercialmente, não apresentando papilomatose cutânea. A presença de DNA de BPV-2 em tecidos do trato reprodutivo, lavado uterino, ovócitos e células do cumulus traz evidências de que a infecção viral pode se desenvolver fora do tecido epitelial. Esses achados alertam para a possibilidade de transmissão do BPV através dos procedimentos de transferência de embriões e de fertilização in vitro.

Bovine papillomavirus type 2 in reproductive tract and gametes of slaughtered bovine females

Papillomaviruses are described selectively infecting epithelial tissues and are associated with many forms of cancer in different species. Considering the widespread dissemination of papillomatosis in livestock, interest is being centred on possible forms of viral transmission and respective mechanisms. In the present study, we report the detection of bovine papillomavirus (BPV) DNA sequences in female reproductive tract tissues, fluids and oocytes from slaughtered bovines not afflicted by cutaneous papillomatosis. BPV-2 DNA sequences were found in ovarian and uterine tissues as well as in oocytes, cumulus cells and uterine flushings. The presence of papillomavirus sequences in reproductive organ tissues and fluids shows that viral infection in organisms can be verified in others tissues, not only in epithelial ones. The present findings alert to the possibility of BPV transmission in embryo transfer programs and assisted fertilization procedures.

Os vírus do papiloma bovino, descritos como agentes infectantes específicos do epitélio, têm sido associados a diversas formas de câncer em diferentes espécies animais. Dada a intensa disseminação da papilomatose nos rebanhos, a investigação de diferentes formas de transmissão e seus respectivos mecanismos tem exigido especial atenção. No presente estudo, é relatada a detecção de seqüências genômicas do papilomavirus bovino (BPV) em ovócitos e tecidos do trato reprodutivo oriundos de fêmeas abatidas comercialmente, não apresentando papilomatose cutânea. A presença de DNA de BPV-2 em tecidos do trato reprodutivo, lavado uterino, ovócitos e células do cumulus traz evidências de que a infecção viral pode se desenvolver fora do tecido epitelial. Esses achados alertam para a possibilidade de transmissão do BPV através dos procedimentos de transferência de embriões e de fertilização in vitro.

Bovine papillomavirus type 2 in reproductive tract and gametes of slaughtered bovine females

Papillomaviruses are described selectively infecting epithelial tissues and are associated with many forms of cancer in different species. Considering the widespread dissemination of papillomatosis in livestock, interest is being centred on possible forms of viral transmission and respective mechanisms. In the present study, we report the detection of bovine papillomavirus (BPV) DNA sequences in female reproductive tract tissues, fluids and oocytes from slaughtered bovines not afflicted by cutaneous papillomatosis. BPV-2 DNA sequences were found in ovarian and uterine tissues as well as in oocytes, cumulus cells and uterine flushings. The presence of papillomavirus sequences in reproductive organ tissues and fluids shows that viral infection in organisms can be verified in others tissues, not only in epithelial ones. The present findings alert to the possibility of BPV transmission in embryo transfer programs and assisted fertilization procedures.

Os vírus do papiloma bovino, descritos como agentes infectantes específicos do epitélio, têm sido associados a diversas formas de câncer em diferentes espécies animais. Dada a intensa disseminação da papilomatose nos rebanhos, a investigação de diferentes formas de transmissão e seus respectivos mecanismos tem exigido especial atenção. No presente estudo, é relatada a detecção de seqüências genômicas do papilomavirus bovino (BPV) em ovócitos e tecidos do trato reprodutivo oriundos de fêmeas abatidas comercialmente, não apresentando papilomatose cutânea. A presença de DNA de BPV-2 em tecidos do trato reprodutivo, lavado uterino, ovócitos e células do cumulus traz evidências de que a infecção viral pode se desenvolver fora do tecido epitelial. Esses achados alertam para a possibilidade de transmissão do BPV através dos procedimentos de transferência de embriões e de fertilização in vitro.

HCV Infection in Northeastern Brazil: unexpected high prevalence of genotype 3a and absence of African genotypes

The genomic diversity of HCV embraces 6 genoptypes and at least 52 subtypes with clinical and epidemiological correlations. There is a paucity of studiens assessing HCV genotypes and biomolecular epidemiology in Brazil. We studied genotypes distribution and epidemiological aspects in 232 HCV carriers, 133 ( 57,9 per cent) males and 99 (42,1 per cent) females, followed in the liver disease referral unit in Salvador, BA, northeastern Brazil. All of them were anti-HCV positive by 3rd generation ELISA assay, and HCV infection showed that 93 (40 per cent) had past blood transfusion, 14 (6 per cent) intravenous drug use, 19 (8 per cent) inhalation of cocaine, 28 (12 per cent) tattooing, 15 (7 per cent) were health care workers, 5 (2 per cent) had reused disposable syringes, 5 (2 per cent) had multiple risk factors and in 53 (23 per cent) no risk factor was determined.Genotypes 1a was observed in 75 (32 per cent), 1b in 72 (31 per cent), 3a in 61 (26 per cent), 2b in 14 (6 per cent): 5 (2.5 per cent) had mixed genotypes and 5 (2.5 per cent) were undetermined. Patients with genotype 1 had a higher mean age (P<0.05) and no particular risk factors were associated with a specific genotype. Genotype 1 largely predominates in northeast Brazil followed by genotype 3 which, in this population, does not seem to be related to intravenous drug abuse, in contrast to some European studies. Although 80 porcentage of the Salvador population comprise African-Brazilians, no Africa genotype was identified, which way mean that HCV was introduced into this region via European immigration. This study demonstrated some peculiarities of HCV epidemiology in Brazil and strongly suggests that HCV introduction to this region was probably related to European immigration.