Publications by authors named "Danielle D Voigt"

Introduction: This study evaluated the effectiveness of chemomechanical preparation associated with intracanal medication in reducing the total bacterial load of infected root canals in cancer patients undergoing antineoplastic treatment. The prevalence, levels, and response to treatment of Streptococcus and Actinobacteria species were also assessed.

Methods: The root canals of teeth with apical periodontitis from oncological and control patients were treated using rotary instrumentation, 2.

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  • This study developed a method to test disinfection techniques for lateral canals in extracted teeth using an ex vivo model.
  • The researchers created lateral canals in mandibular premolars and contaminated them with a bacterial culture to evaluate the effectiveness of different disinfection procedures.
  • Results showed that all tested methods significantly reduced bacterial presence in the canals, with no significant differences in effectiveness among the various disinfection techniques used.
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Introduction: This ex vivo study evaluated the disinfecting and cleaning effects of root canal preparation using sodium hypochlorite irrigation with 3 different needle designs.

Methods: Mesial roots from extracted mandibular molars with Vertucci class II configuration were anatomically matched based on micro-computed tomography (micro-CT) analyses and distributed into 3 groups (n = 18/group). The canals were contaminated with a mixed bacterial culture for 30 days and then subjected to preparation using 2.

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Introduction: This study used a correlative multianalytical approach to investigate the bacteriologic conditions in the apical root canal system of treated teeth with or without apical periodontitis and their correlation with the technical quality of the previous root canal obturation and the presence and volume of apical periodontitis lesions.

Methods: Root apexes were obtained from recently extracted root canal-treated teeth with (n = 23) and without (n = 22) apical periodontitis lesions as demonstrated by cone-beam computed tomographic examination. The root apexes were sectioned and subjected to micro-computed tomographic (micro-CT) scanning.

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By the year 2050, the world's elderly population may increase exponentially, raising the rate of disease characteristic of this group, such as prostate cancer (PCa) and benign prostatic hyperplasia (BPH). Prostate disorders have a multifactorial etiology, especially age and genetic factors. Currently, PCa is the second most frequent neoplasm in the male population worldwide.

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  • Regular physical activity helps prevent obesity by increasing energy expenditure, where the PPARGC1A gene plays a key role in producing the hormone irisin, which promotes fat burning.
  • This study examined genetic variants in genes related to fat metabolism among 210 individuals with severe obesity and 191 normal-weight subjects to assess their impact on obesity-related traits.
  • The results identified specific genetic variants linked to severe obesity and found a novel mutation in the FNDC5 gene, indicating that these genetic factors contribute significantly to obesity susceptibility.
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  • Obesity is a significant global health issue influenced by genetics and environment, with the FTO gene identified as a key genetic factor.
  • This study analyzed FTO gene variations (specifically rs9939609 and rs17817449) in 169 normal-weight and 123 extremely obese subjects to assess their impact on obesity and related health metrics.
  • Results indicated a strong link between FTO variants and extreme obesity, with specific haplotypes increasing obesity risk, and certain polymorphisms affecting BMI and triglyceride levels, though no effect on the onset age of obesity was observed.
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Robust evidence on the involvement of genetic factors in the etiology of Parkinson's disease (PD) expands our knowledge about monogenic causes that contribute for this important neurodegenerative disorder. Mutations in the CHCHD2 gene have been linked to autosomal dominant forms of PD, although there is still lack of evidence for CHCHD2 variants leading to the disease in mixed populations as those from South America. To assess the contribution of CHCHD2 as a causal factor for familial PD in Brazil, one of the most heterogeneous populations in the world, we conducted the first molecular analysis of the CHCHD2 gene in a cohort of 122 index cases from Brazilian families with autosomal dominant forms of PD.

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Background: Parkinson's disease (PD) is a neurodegenerative disorder characterized by remarkable phenotypic variability. Accumulated evidence points that the manifestation of PD clinical signs might be differentially modified by genetic factors, as mutations in LRRK2 and GBA genes. In this sense, the clarification of the genotype-phenotype correlations in PD has important implications in predicting prognosis and can contribute to the development of specific therapeutic approaches.

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