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1.
JDR Clin Trans Res ; 7(4): 360-370, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-34549639

RESUMO

INTRODUCTION: The impact of periodontal disease on oral health-related quality of life (OHRQoL) has often been investigated from a quantitative research perspective, which is based on clinical findings and an OHRQoL questionnaire. Very few studies have examined the issue from the view of qualitative research. To our knowledge, there have been no previous qualitative studies focusing the effect of periodontal disease on OHRQoL in Indonesian older people. OBJECTIVES: To explore and understand the impact of periodontal disease on the OHRQoL of older people as a subjective reflection in relation to periodontal disease experiences. METHODS: Semi-structured interviews were conducted in a sample of 31 older people with generalized chronic periodontitis. Thematic analysis was used to identify the key issues in participants' accounts. The analysis was undertaken by 2 independent coders to ensure reliability. To achieve thematic saturation, successive interviews were undertaken until 5 sequential interviews did not bring new themes. RESULTS: Participants reported the negative effects likely related to periodontal disease. The impacts of periodontal disease were described by these older people as affecting more than pain, physical discomfort, and physical function restrictions. Periodontal disease also affected their psychological and social aspects of daily living. In addition, this study identified themes related to individual and environmental factors that may modify and personalize periodontal disease experiences. Furthermore, this study identified a misleading belief that problems related to periodontal disease were a normal part of aging, which might influence individuals' expectations toward oral health. Relatedly, participants frequently reported that the progression of tooth mobility to tooth loss was an inevitable part of the aging process. CONCLUSIONS: Periodontal disease negatively affected participants' OHRQoL. It is fundamental to understand older people's perceptions toward their periodontal disease as well as individual and environmental factors that may have an influence on their periodontal disease experiences. KNOWLEDGE TRANSFER STATEMENT: This study is a reflection of Indonesian older people's subjective periodontal disease experiences. Therefore, the present study can be used to understand older people's perceptions, attitudes, behaviors, and experiences toward periodontal disease and how this disease may affect their quality of life. This study also highlights a widespread and misleading belief that oral problems related to periodontal disease are an inevitable part of aging in this study population.


Assuntos
Periodontite Crônica , Qualidade de Vida , Idoso , Humanos , Indonésia/epidemiologia , Pesquisa Qualitativa , Qualidade de Vida/psicologia , Reprodutibilidade dos Testes
2.
JDR Clin Trans Res ; 7(3): 277-288, 2022 07.
Artigo em Inglês | MEDLINE | ID: mdl-34282670

RESUMO

INTRODUCTION: Despite being acknowledged as the second global burden of oral disease, periodontal disease has few epidemiologic studies in the literature, particularly for developing countries. Many previous studies have assessed the relationship between periodontal disease and oral health-related quality of life (OHRQoL), with patients attending dental clinic or hospitals rather than a general population. This study attempted to fill the knowledge gap in limited information about periodontal disease and OHRQoL, with reference to a general population in a developing country. OBJECTIVES: To investigate the relationship between OHRQoL and periodontal diseases in an older population in Indonesia. METHODS: We invited 582 older people from community health centers. The 369 (63.4%) older people who agreed to participate consented to an oral health examination and a questionnaire capturing demographic, socioeconomic, behavioral, and Oral Health Impact Profile-14 (OHIP-14) data. RESULTS: Almost 75% of the older people had generalized periodontitis; 3% had healthy periodontal status; and around 22% had localized periodontitis. There was a lack of statistical evidence for an association between periodontal disease status and OHRQoL. This result was based on the appraisal of the prevalence of the impact (Odds ratio [OR], 0.95 [95% CI, 0.54 to 1.59]; P = 0.77), difference in mean severities (0.07 [95% CI, -1.66 to 1.80]; P = 0.94), and extent of the impact (P = 0.996). However, we found evidence for a relationship between tooth mobility and OHRQoL for all of the OHIP assessments, including prevalence of the impact (OR, 1.87 [95% CI, 1.16 to 3.01]; P = 0.009), difference in mean severities (-2.98 [95% CI, -4.50 to -1.45]; P < 0.001), and extent of the impact (P = 0.001). CONCLUSION: There was a lack of statistical evidence for a relationship between periodontal disease status and OHRQoL in this society. However, we found evidence that tooth mobility, as a sign of periodontal disease progression, is related to OHRQoL. KNOWLEDGE TRANSFER STATEMENT: The present study can be used by dentists, community health workers, and policy makers in Indonesia to understand the prevalence, severity, and extent of the negative impacts of periodontal disease on older people's quality of life. In addition, this study provides information about factors that might considerably affect the oral health-related quality of life in this society, such as brushing habits, dental visit, family income, DMF-T status, and subjective appraisal toward dental health.


Assuntos
Doenças Periodontais , Periodontite , Mobilidade Dentária , Idoso , Humanos , Indonésia/epidemiologia , Saúde Bucal , Doenças Periodontais/epidemiologia , Qualidade de Vida
3.
Eur Cell Mater ; 42: 43-62, 2021 07 18.
Artigo em Inglês | MEDLINE | ID: mdl-34275129

RESUMO

Dentineogenesis starts on odontoblasts, which synthesise and secrete non-collagenous proteins (NCPs) and collagen. When dentine is injured, dental pulp progenitors/mesenchymal stem cells (MSCs) can migrate to the injured area, differentiate into odontoblasts and facilitate formation of reactionary dentine. Dental pulp progenitor cell/MSC differentiation is controlled at given niches. Among dental NCPs, dentine sialophosphoprotein (DSPP) is a member of the small integrin-binding ligand N-linked glycoprotein (SIBLING) family, whose members share common biochemical characteristics such as an Arg-Gly-Asp (RGD) motif. DSPP expression is cell- and tissue-specific and highly seen in odontoblasts and dentine. DSPP mutations cause hereditary dentine diseases. DSPP is catalysed into dentine glycoprotein (DGP)/sialoprotein (DSP) and phosphoprotein (DPP) by proteolysis. DSP is further processed towards active molecules. DPP contains an RGD motif and abundant Ser-Asp/Asp-Ser repeat regions. DPP-RGD motif binds to integrin αVß3 and activates intracellular signalling via mitogen-activated protein kinase (MAPK) and focal adhesion kinase (FAK)-ERK pathways. Unlike other SIBLING proteins, DPP lacks the RGD motif in some species. However, DPP Ser-Asp/Asp-Ser repeat regions bind to calcium-phosphate deposits and promote hydroxyapatite crystal growth and mineralisation via calmodulin-dependent protein kinase II (CaMKII) cascades. DSP lacks the RGD site but contains signal peptides. The tripeptides of the signal domains interact with cargo receptors within the endoplasmic reticulum that facilitate transport of DSPP from the endoplasmic reticulum to the extracellular matrix. Furthermore, the middle- and COOH-terminal regions of DSP bind to cellular membrane receptors, integrin ß6 and occludin, inducing cell differentiation. The present review may shed light on DSPP roles during odontogenesis.


Assuntos
Odontoblastos , Sialoglicoproteínas , Diferenciação Celular , Polpa Dentária , Dentina , Proteínas da Matriz Extracelular , Fosfoproteínas
4.
J Dent Res ; 98(9): 968-974, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31238019

RESUMO

While the prevalence of supernumerary teeth (ST) is high in permanent dentition, the etiology of ST in humans remains unclear. However, multiple murine models of ST have elaborated on dated mechanisms traditionally ascribed to ST etiology: one involves the rescue of rudimental teeth, and the second considers the contribution of odontogenic epithelial stem cells. It remains unclear whether these mechanisms of ST formation in mice are applicable to humans. The third dentition is usually regressed apoptotic-that is, the teeth do not completely form in humans. Recently, it was suggested that ST result from the rescue of regression of the third dentition in humans. The present investigation evaluates the proportion of collected general ST cases that evinced a third dentition based on the clinical definition of ST derived from the third dentition. We also investigated the contribution of SOX2-positive odontogenic epithelial stem cells to ST formation in humans. We collected 215 general ST cases from 15,008 patients. We confirmed that the general characteristics of the collected ST cases were similar to the results from previous reports. Of the 215 cases, we narrowed our analysis to the 78 patients who had received a computed tomography scan. The frequency of ST considered to have been derived from the third dentition was 26 out of 78 cases. Evidence of a third dentition was especially apparent in the premolar region, was more common in men, and was more likely among patients with ≥3 ST. SOX2-positive odontogenic epithelial stem cells within the surrounding epithelial cells of developing ST were observed in non-third dentition cases and not in third dentition cases. In conclusion, the third dentition is the main cause of ST in humans. The odontogenic epithelial stem cells may contribute to ST formation in cases not caused by a third dentition.


Assuntos
Dente Pré-Molar , Dentição Permanente , Odontogênese , Dente Supranumerário , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Criança , Células Epiteliais/citologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Transcrição SOXB1 , Células-Tronco/citologia , Adulto Jovem
5.
Sci Rep ; 8(1): 3328, 2018 03 05.
Artigo em Inglês | MEDLINE | ID: mdl-29507301

RESUMO

Many lizards can drop a portion of their tail in response to an attack by a predator, a behaviour known as caudal autotomy. The capacity for intravertebral autotomy among modern reptiles suggests that it evolved in the lepidosaur branch of reptilian evolution, because no such vertebral features are known in turtles or crocodilians. Here we present the first detailed evidence of the oldest known case of caudal autotomy, found only among members of the Early Permian captorhinids, a group of ancient reptiles that diversified extensively and gained a near global distribution before the end-Permian  mass extinction event of the Palaeozoic. Histological and SEM evidence show that these early reptiles were the first amniotes that could autotomize their tails, likely as an anti-predatory behaviour. As in modern iguanid lizards, smaller captorhinids were able to drop their tails as juveniles, presumably as a mechanism to evade a predator, whereas larger individuals may have gradually lost this ability. Caudal autotomy in captorhinid reptiles highlights the antiquity of this anti-predator behaviour in a small member of a terrestrial community composed predominantly of larger amphibian and synapsid predators.


Assuntos
Comportamento Animal , Comportamento Predatório , Regeneração , Répteis/anatomia & histologia , Répteis/fisiologia , Cauda , Animais , Cauda/anatomia & histologia , Cauda/fisiologia
6.
Contraception ; 96(2): 81-88, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28385554

RESUMO

OBJECTIVE: The objective was to determine the acceptability to women of oral emergency contraception (EC) that works by inhibiting ovulation, preventing implantation or disrupting implantation, and also to determine the characteristics of women associated with the acceptability of each posited mechanism of action. STUDY DESIGN: Women completed a self-administered, anonymous questionnaire asking whether they would consider using an EC pill based on each of three hypothetical mechanisms of action: inhibiting ovulation, preventing implantation or disrupting implantation. The questionnaire was distributed among women in Edinburgh, UK, (a) presenting for EC at a community pharmacy, (b) attending a clinic for insertion of intrauterine contraception (IUC) or (c) attending a clinic for an induced abortion. Descriptive analyses stratified women according to healthcare setting and personal characteristics. Univariable and multivariable analyses were used to establish factors which may predict acceptability of each EC pill's mechanism of action. RESULTS: Four hundred and nineteen out of 458 (91%) women responded to the survey. Overall, women reported that EC would be acceptable if it worked by inhibiting ovulation (89%), preventing implantation (83%) or disrupting implantation (75%). Among women seeking abortion, more would accept an EC pill which disrupted implantation compared to women seeking IUC (odds ratio, 2.19; 95% confidence interval, 1.30-3.69; p=.004). Based on multivariable analyses, factors associated with acceptability included previous use of EC, previously holding strong views against abortion and having had a previous abortion. CONCLUSION: For each of the posited mechanisms of action, a majority of women surveyed would be willing to consider oral EC to prevent unintended pregnancy. IMPLICATIONS STATEMENT: The scope of the study was limited, and further work on the views of women in the wider population is needed. This is important as the development of such drugs to prevent pregnancy is likely to raise political and ethical challenges, particularly in relation to disruption of implantation.


Assuntos
Anticoncepção Pós-Coito/métodos , Anticoncepcionais Orais Combinados/uso terapêutico , Aceitação pelo Paciente de Cuidados de Saúde , Adolescente , Adulto , Feminino , Humanos , Pessoa de Meia-Idade , Farmácias , Gravidez , Escócia , Inquéritos e Questionários , Adulto Jovem
7.
J Periodontal Res ; 51(5): 647-60, 2016 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26754272

RESUMO

BACKGROUND AND OBJECTIVE: Periodontitis is a severe chronic inflammatory disease and one of the most prevalent non-communicable chronic diseases that affects the majority of the world's adult population. While great efforts have been devoted toward understanding the pathogenesis of periodontitis, there remains a pressing need for developing potent therapeutic strategies for targeting this dreadful disease. In this study, we utilized adeno-associated virus (AAV) expressing cathepsin K (Ctsk) small hairpin (sh)RNA (AAV-sh-Ctsk) to silence Ctsk in vivo and subsequently evaluated its impact in periodontitis as a potential therapeutic strategy for this disease. MATERIAL AND METHODS: We used a known mouse model of periodontitis, in which wild-type BALB/cJ mice were infected with Porphyromonas gingivalis W50 in the maxillary and mandibular periodontium to induce the disease. AAV-sh-Ctsk was then administrated locally into the periodontal tissues in vivo, followed by analyses to assess progression of the disease. RESULTS: AAV-mediated Ctsk silencing drastically protected mice (> 80%) from P. gingivalis-induced bone resorption by osteoclasts. In addition, AAV-sh-Ctsk administration drastically reduced inflammation by impacting the expression of many inflammatory cytokines as well as T-cell and dendritic cell numbers in periodontal lesions. CONCLUSION: AAV-mediated Ctsk silencing can simultaneously target both the inflammation and bone resorption associated with periodontitis through its inhibitory effect on immune cells and osteoclast function. Thereby, AAV-sh-Ctsk administration can efficiently protect against periodontal tissue damage and alveolar bone loss, establishing this AAV-mediated local silencing of Ctsk as an important therapeutic strategy for effectively treating periodontal disease.


Assuntos
Catepsina K/genética , Catepsina K/farmacologia , Inativação Gênica , Terapia Genética , Inflamação/metabolismo , Doenças Periodontais/terapia , Perda do Osso Alveolar/patologia , Animais , Reabsorção Óssea/microbiologia , Reabsorção Óssea/patologia , Reabsorção Óssea/prevenção & controle , Catepsina K/fisiologia , Citocinas/genética , Células Dendríticas/imunologia , Dependovirus/genética , Modelos Animais de Doenças , Feminino , Inflamação/patologia , Inflamação/virologia , Camundongos , Camundongos Endogâmicos BALB C , Osteoclastos , Doenças Periodontais/imunologia , Doenças Periodontais/microbiologia , Doenças Periodontais/patologia , Periodontite/imunologia , Periodontite/patologia , Periodontite/terapia , Periodonto/microbiologia , Periodonto/patologia , Porphyromonas gingivalis/patogenicidade , RNA Interferente Pequeno/genética , Linfócitos T/imunologia
11.
Int J STD AIDS ; 22(6): 351-2, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21680675

RESUMO

This retrospective study assessed whether Quality Improvement Scotland national standards for the sexual health care offered to HIV-positive individuals are being met by the Edinburgh genitourinary (GU) medicine clinic; specifically whether HIV-positive patients are offered: (a) sexually transmitted infection (STI) screening annually and (b) syphilis testing six-monthly. The study also reviewed what factors were associated with a clinician's offer of STI screening and syphilis testing. Of the 509 patients seen within the study period, case notes documented that 64% were offered STI screens, and 69% were offered syphilis testing, results consistent with audits of services elsewhere. Sexual orientation (P < 0.0005), relationship status (P = 0.007) and receipt of antiretrovirals (P = 0.001) were independent predictors of clinician offer of STI screening, while gender (P < 0.0005) and receipt of antiretrovirals (P = 0.063) were independent predictors of offer of syphilis testing. Our results suggest that one explanation for clinicians failing to offer STI screens and syphilis serology testing is their (implicit) risk assessment that STI testing is not required in individual patients.


Assuntos
Infecções por HIV/complicações , Acessibilidade aos Serviços de Saúde , Padrões de Prática Médica , Infecções Sexualmente Transmissíveis/diagnóstico , Sífilis/diagnóstico , Adulto , Feminino , Humanos , Masculino , Programas de Rastreamento/métodos , Aceitação pelo Paciente de Cuidados de Saúde , Estudos Retrospectivos , Infecções Sexualmente Transmissíveis/virologia , Sífilis/virologia
12.
Cells Tissues Organs ; 194(2-4): 296-301, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21597274

RESUMO

Odontogenic tumors occur within the jaw bones and may be derived from odontogenic epithelium or ectomesenchyme or contain active components of both tissue types. We investigated the gene expression profile of enamel matrix proteins (EMPs), genes related to osteogenesis, and the mineralization process in odontogenic tumor cell populations focusing on an ameloblastoma (AB-1), a keratocystic odontogenic tumor (KCOT-1), and a calcifying epithelial odontogenic tumor (CEOT-1). All cell populations were shown to be epithelial in origin by CK14 expression. All tested EMPs were expressed by all odontogenic tumor cell types, with higher transcript levels seen in the AB-1 population especially for AMEL, AMBN, and ODAM. CEOT-1 cell populations showed a greater content of ALP-positive cells as well as higher ALP mRNA levels. Using qRT-PCR, we found a higher expression of 8 genes in the CEOT-1 compared to the AB-1 and KCOT-1. In this study we demonstrated the establishment of AB-1, KCOT-1 and CEOT-1 cell populations. The unique gene expression profiles of AB-1, KCOT-1, and CEOT-1 cells and their interactions with the surrounding microenvironment may support their unique tumor development, progression, and survival.


Assuntos
Esmalte Dentário/metabolismo , Esmalte Dentário/patologia , Perfilação da Expressão Gênica , Regulação Neoplásica da Expressão Gênica , Tumores Odontogênicos/genética , Osteogênese/genética , Linhagem Celular Tumoral , Proliferação de Células , Forma Celular , Proteínas do Esmalte Dentário/genética , Proteínas do Esmalte Dentário/metabolismo , Humanos , Imuno-Histoquímica , Proteínas de Neoplasias/genética , Proteínas de Neoplasias/metabolismo , Tumores Odontogênicos/patologia , RNA Mensageiro/genética , RNA Mensageiro/metabolismo
13.
Bull Group Int Rech Sci Stomatol Odontol ; 49(3): 94-7, 2011 Apr 11.
Artigo em Inglês | MEDLINE | ID: mdl-22750370

RESUMO

Both of bone morphogenetic proteins 2 and 4 (Bmp2 and Bmp4) are two closely related members of the transforming growth factor beta superfamily and play diverse roles in normal and pathological processes. However, detail understandings of mechanisms through which Bmp2 and Bmp4 exert their effects remain elusive due to their functional compensations each other. To study roles of Bmp2/Bmp4 in osteoblast differentiation and extracellular matrix (ECM) remodeling, calvarial osteoblasts from Bmp2/4 conditional mice with Cre recombinase recognition site (loxP) were isolated and transfected with simian virus 40 large T antigen to generate immortalized BMP2C/C4C/C (iBMP2 C/C/4C/C) osteoblast lines. The BMP2/4 genes in the iBMP2 C/C/4C/C cells were double knocked out by Ad-Cre recombinase infection. Differentiation and mineralization of iBMP2C/C/4C/C knock-out (iBmp2C/C/4C/C KO) cells were detected by alkaline phosphatase (ALP) and alizarin (ALZ) red S staining analyses. ECM remodeling was also observed in fluorescent microscope. Cell differentiation was dramatically decreased in the iBMP2C/C/4C/C KO cells compared to that of the iBMP2C/C/4C/C osteoblasts. Mineralization was also reduced in these KO cells by ALZ staining. Furthermore, Bmp2/4 double knock-out cells have major defects in remodeling the ECM as reflected by changes in collagen type I processing. Here we for the first time demonstrate the establishment of iBmp2C/C/4C/C KO osteoblasts. Cell differentiation and mineralization in the iBmp2C/C/4C/C KO cells were decreased. Furthermore, ECM processing in these KO cells was impaired. This indicates that BMP2/4 play important roles in osteoblast differentiation and ECM remodeling.


Assuntos
Proteína Morfogenética Óssea 2/fisiologia , Proteína Morfogenética Óssea 4/fisiologia , Matriz Extracelular/fisiologia , Osteoblastos/fisiologia , Fosfatase Alcalina/análise , Animais , Antraquinonas , Proteína Morfogenética Óssea 2/análise , Proteína Morfogenética Óssea 4/análise , Remodelação Óssea/fisiologia , Calcificação Fisiológica/fisiologia , Técnicas de Cultura de Células , Diferenciação Celular/fisiologia , Linhagem Celular , Colágeno Tipo I/análise , Colágeno Tipo I/metabolismo , Corantes , Matriz Extracelular/metabolismo , Fluoresceína-5-Isotiocianato , Corantes Fluorescentes , Camundongos , Camundongos Knockout
14.
J R Coll Physicians Edinb ; 40(3): 196-200, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21127758

RESUMO

AIM: To determine whether the survival of patients with suspected acute pulmonary embolism (PE) relates to radiological probability of acute PE assessed using lung scintigraphy scans (LSS). METHODS: Lung scintigraphy scan results from a venous thromboembolism database were categorised as high, indeterminate or low probability using the modified PIOPED criteria and corresponding chest X-rays (CXRs) as normal or abnormal. Mortality data on these cases were obtained from the General Register Office for Scotland, and survival was analysed using the Kaplan-Meier method. RESULTS: Of the 1,818 LSS analysed, 941 (51.8%) were normal, 532 (29.3%) indeterminate and 345 (19.0%) high probability. After an adjustment for age and gender, no significant survival difference was found between patients with normal and high probability LSS (p=0.182). However, patients with indeterminate LSS had significantly lower survival than patients in the other groups. This difference persisted after adjustment for CXR result. CONCLUSIONS: Indeterminate LSS results are associated with a poor prognosis. Careful follow-up of patients with inderminate LSS would appear to be justified.


Assuntos
Embolia Pulmonar/diagnóstico por imagem , Feminino , Humanos , Funções Verossimilhança , Masculino , Pessoa de Meia-Idade , Prognóstico , Modelos de Riscos Proporcionais , Embolia Pulmonar/mortalidade , Radiografia Torácica , Cintilografia , Estudos Retrospectivos , Escócia/epidemiologia , Taxa de Sobrevida , Tomografia Computadorizada por Raios X
15.
J Dent Res ; 89(6): 597-602, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20173182

RESUMO

Nma/BAMBI is a novel pseudoreceptor with homology to a TGFbeta type I receptor that lacks a serine/threonine kinase domain. Nma/BAMBI functions as a dominant-negative protein that regulates reciprocal epithelial-mesenchymal interactions during organogenesis. Therefore, we hypothesized that Nma/BAMBI regulates TGFbeta signaling and downstream gene expression during dentinogenesis. To test this hypothesis, we examined the downstream gene expression profiles of major dentin extracellular matrix proteins in response to Nma/BAMBI, and we examined the roles of Nma/BAMBI and TGFbeta-1 during dentinogenesis. Overexpression of Nma/BAMBI in the mouse odontoblast-like cell line MD10-A2 down-regulated expression of DSPP by 66% and up-regulated expression of DMP1 four-fold. TGFbeta treatment reversed Nma/BAMBI's negative effect on DSPP expression. Furthermore, we demonstrated that TGFbeta negatively regulates Nma/BAMBI's expression levels in MD10-A2 odontoblast-like cells. Analysis of these data, together, indicates that TGFbeta and Nma/BAMBI are inversely regulated and that the sequence of expression determines the net effect on downstream gene expression.


Assuntos
Proteínas de Membrana/fisiologia , Odontoblastos/fisiologia , Fator de Crescimento Transformador beta/fisiologia , Fosfatase Alcalina/análise , Animais , Linhagem Celular , Dentina/metabolismo , Dentinogênese/genética , Dentinogênese/fisiologia , Regulação para Baixo/genética , Proteínas da Matriz Extracelular/análise , Proteínas da Matriz Extracelular/genética , Perfilação da Expressão Gênica , Regulação da Expressão Gênica/genética , Vetores Genéticos/genética , Luciferases , Substâncias Luminescentes , Proteínas de Membrana/genética , Camundongos , Fosfoproteínas/análise , Fosfoproteínas/genética , Proteínas Serina-Treonina Quinases/fisiologia , Receptor do Fator de Crescimento Transformador beta Tipo I , Receptores de Fatores de Crescimento Transformadores beta/fisiologia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Homologia de Sequência , Sialoglicoproteínas/análise , Sialoglicoproteínas/genética , Transdução de Sinais/genética , Transdução de Sinais/fisiologia , Transfecção , Fator de Crescimento Transformador beta/genética , Regulação para Cima/genética
16.
J Dent Res ; 88(10): 904-9, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19783797

RESUMO

The transcription factors Runx2 and Osx are necessary for osteoblast and odontoblast differentiation, while Dspp is important for odontoblast differentiation. The relationship among Runx2, Osx, and Dspp during tooth and craniofacial bone development remains unknown. In this study, we hypothesized that the roles of Runx2 and Osx in the regulation of osteoblast and odontoblast lineages may be independent of one another. The results showed that Runx2 expression overlapped with Osx in dental and osteogenic mesenchyme from E12 to E16. At the later stages, from E18 to PN14, Runx2 and Osx expressions remained intense in alveolar bone osteoblasts. However, Runx2 expression was down-regulated, whereas Osx expression was clearly seen in odontoblasts. At later stages, Dspp transcription was weakly present in osteoblasts, but strong in odontoblasts where Osx was highly expressed. In mouse odontoblast-like cells, Osx overexpression increased Dspp transcription. Analysis of these data suggests differential biological functions of Runx2, Osx, and Dspp during odontogenesis and osteogenesis.


Assuntos
Subunidade alfa 1 de Fator de Ligação ao Core/fisiologia , Odontogênese/fisiologia , Fosfoproteínas/fisiologia , Precursores de Proteínas/fisiologia , Sialoglicoproteínas/fisiologia , Fatores de Transcrição/fisiologia , Dedos de Zinco/fisiologia , Processo Alveolar/citologia , Ameloblastos/citologia , Ameloblastos/fisiologia , Animais , Diferenciação Celular/fisiologia , Linhagem Celular Tumoral , Linhagem da Célula/fisiologia , Células Cultivadas , Subunidade alfa 1 de Fator de Ligação ao Core/análise , Polpa Dentária/citologia , Proteínas da Matriz Extracelular , Mesoderma/citologia , Mesoderma/fisiologia , Camundongos , Camundongos Endogâmicos ICR , Odontoblastos/citologia , Odontoblastos/fisiologia , Osteoblastos/citologia , Osteoblastos/fisiologia , Osteogênese/fisiologia , Fosfoproteínas/análise , Precursores de Proteínas/análise , Sialoglicoproteínas/análise , Fator de Transcrição Sp7 , Fatores de Transcrição/análise
17.
Int J STD AIDS ; 20(7): 503-5, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19541895

RESUMO

We undertook this study to try to determine whether disease outcomes were poorer in patients with HIV infection whose general practitioner (GP) was unaware of their status compared with those whose GP was aware. The notes of 375 HIV-positive patients attending Edinburgh's genitourinary (GU) medicine clinic were reviewed. The GPs of 292 patients (78%) had been informed of their patient's HIV infection. Advancing disease was associated with disclosure of the status to GPs (P = 0.037) but no significant association was found between informing GPs and the viral load results of treated (P = 0.389) and untreated patients (P = 0.070). Twenty-three percent of patients had had one or more bacterial sexually transmitted infections (STIs) while receiving their HIV care at a GU medicine clinic. Patients diagnosed with an STI were less likely to disclose their HIV status to their GP (P < 0.0005). Non-disclosure of the HIV status to a GP may be a predictor of unsafe sexual practices.


Assuntos
Medicina de Família e Comunidade , Infecções por HIV/diagnóstico , Soropositividade para HIV , Revelação da Verdade , Adulto , Progressão da Doença , Feminino , Infecções por HIV/complicações , Infecções por HIV/tratamento farmacológico , Infecções por HIV/virologia , HIV-1 , Humanos , Masculino , Pessoa de Meia-Idade , Doenças Bacterianas Sexualmente Transmissíveis/complicações , Doenças Bacterianas Sexualmente Transmissíveis/microbiologia , Sexo sem Proteção , Carga Viral , Adulto Jovem
18.
QJM ; 102(6): 407-14, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19376792

RESUMO

BACKGROUND: Relatively little is known about prognosis in patients for whom suspected pulmonary embolism (PE) is refuted by imaging. AIM: This prospective study of suspected PE therefore compared clinico-radiological features and outcome in patients with and without PE. DESIGN AND METHODS: Computed tomographic pulmonary angiography (CTPA) confirmed or refuted PE in consecutive patients. Clinical, laboratory and radiological features were recorded at baseline, and mortality at 1 year determined. Univariate and multivariate analyses identified variables associated with PE. RESULTS: PE was diagnosed in 45 patients and refuted in 141. The PE and 'non-PE' groups were similar with regard to extravascular radiology (though consolidation was significantly more common in the PE group [present in 24 (53%) of the PE group and 42 (30%) of the non-PE group, P < 0.01)], comorbidities (no significant differences), and baseline characteristics (only serum D-dimer concentrations were independently associated with PE by multivariate analysis, P = 0.001). Right ventricular dimensions were significantly higher in the PE group, [right ventricular to left ventricular ratio was 0.98 (range 0.64-2.48) in the PE group and 0.92 (range 0.66-1.95) in the non-PE group, P < 0.05]. In the PE group, right ventricular dimensions rose sharply when 10 or more segmental pulmonary arteries were occluded. One year all-cause mortality was 6.7% in the PE group and 13.5% in the non-PE group (no significant difference, P = 0.218). CONCLUSION: Among a cohort of patients presenting with clinically suspected PE, clinical characteristics, co-morbidities and radiological features were similar when comparing groups with CTPA-proven or CTPA-refuted PE. However RV dimensions, radiological consolidation on imaging and D-dimer levels were significantly higher in the PE group. Patients with suspected PE have a poor prognosis irrespective of whether PE is confirmed. This appears accentuated in patients without PE, a finding possibly under-recognized in clinical practice.


Assuntos
Artéria Pulmonar/diagnóstico por imagem , Embolia Pulmonar/diagnóstico por imagem , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Comorbidade , Métodos Epidemiológicos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Embolia Pulmonar/diagnóstico , Embolia Pulmonar/mortalidade , Radiografia , Resultado do Tratamento , Adulto Jovem
19.
J Pediatr Gastroenterol Nutr ; 48(2): 161-7, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19179877

RESUMO

OBJECTIVES: To determine anti-Saccharomyces cerevisiae antibodies (ASCA) status and its relation to disease phenotype in patients with inflammatory bowel disease (IBD). PATIENTS AND METHODS: A total of 301 Scottish patients with early-onset IBD-197 Crohn disease (CD), 76 ulcerative colitis (UC), 28 indeterminate colitis (IC)-and 78 healthy control individuals were studied. ASCA status (IgA, IgG) was determined by enzyme-linked immunosorbent assay. ASCA status was then analyzed in relation to CD phenotype. RESULTS: Patients with CD had a higher prevalence of ASCA than patients with UC and healthy controls: 82/197 versus 12/76, odds ratio (OR) 3.80 (1.93-7.50) and 82/197 versus 6/78, OR 8.56 (3.55-20.62), respectively. Univariate analysis showed that positive ASCA status was associated with oral CD (17/25 vs 59/153, OR 3.39 [1.38-8.34]), perianal CD (39/77 vs 38/108, OR 1.89 [1.04-3.44]) and the presence of granulomata (63/132 vs 15/52, OR 2.25 [1.13-4.48]) and also with markers of disease severity: raised C-reactive protein (44/90 vs 12/49, OR 2.95[1.36-6.37]), hypoalbuminemia (44/85 vs 20/74, OR 2.28[1.19-4.37]), and surgery (27/49 vs 54/147, OR 2.11 [1.10-4.06]). From multivariate analysis, the presence of oral disease (adjusted P = 0.001, OR 22.22 [3.41-142.86]) and hypoalbuminemia (adjusted P = 0.01, OR 4.78 [1.40-16.39]) was found to be independently associated with ASCA status. No association was demonstrated between ASCA and IBD candidate genes. CONCLUSIONS: Patients with CD had a higher prevalence of ASCA than did other patients with IBD. ASCA status described patients with CD who had a specific phenotype, showing an association with markers of disease severity and oral CD involvement.


Assuntos
Anticorpos Antifúngicos/sangue , Colite Ulcerativa/imunologia , Doença de Crohn/imunologia , Saccharomyces cerevisiae/imunologia , Adolescente , Biomarcadores/sangue , Estudos de Casos e Controles , Criança , Colite Ulcerativa/sangue , Colite Ulcerativa/microbiologia , Colite Ulcerativa/patologia , Doença de Crohn/sangue , Doença de Crohn/microbiologia , Doença de Crohn/patologia , Ensaio de Imunoadsorção Enzimática , Feminino , Genótipo , Nível de Saúde , Humanos , Imunoglobulina A/sangue , Imunoglobulina G/sangue , Masculino , Análise Multivariada , Razão de Chances , Estudos Soroepidemiológicos , Índice de Gravidade de Doença
20.
Cells Tissues Organs ; 189(1-4): 230-6, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-18797159

RESUMO

The aim of this study was to perform phenotype analysis and dentin sialophosphoprotein (DSPP) mutational analysis on 3 Brazilian families diagnosed with dentinogenesis imperfecta type II (DGI-II) attending the Dental Anomalies Clinic in Brasilia, Brazil. Physical and oral examinations, as well as radiographic and histopathological analyses, were performed on 28 affected and unaffected individuals. Clinical, radiographic and histopathological analyses confirmed the diagnosis of DGI-II in 19 individuals. Pulp stones were observed in ground sections of several teeth in 2 families, suggesting that obliteration of pulp chambers and root canals results from the growth of these nodular structures. Mutational DSPP gene analysis of representative affected family members revealed 7 various non-disease-causing alterations in exons 1-4 within the dentin sialoprotein domain. Further longitudinal studies are necessary to elucidate the progression of pulpal obliteration in the DGI-II patients studied as well as the molecular basis of their disease.


Assuntos
Indígena Americano ou Nativo do Alasca/genética , Dentinogênese Imperfeita/genética , Dentinogênese Imperfeita/patologia , Proteínas da Matriz Extracelular/genética , Brasil , Análise Mutacional de DNA , Família , Feminino , Humanos , Masculino , Linhagem , Fenótipo , Fosfoproteínas , Radiografia , Sialoglicoproteínas , Dente/diagnóstico por imagem , Dente/patologia
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