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Healthy urban mobility is the concept that deals with how the physical structure of cities affect the mobility of the population and how it relates to collective health and well-being. The article seeks to share the experience of conducting a research on healthy urban mobility in the Cruzeiro Region in Porto Alegre (RS-Brazil) and the experiences and reflections raised during the survey. In order to make viable the large-scale survey in the territory, it became necessary the researchers' partnership with the local population, a relationship that caused tensions and adaptations. The text provides an analytical description of the survey steps, using the field diary and the research report as sources of information. As a result, the importance of community participation in association with academic research in the search for social transformations is highlighted, even though symbolic barriers must be overcomed. We hope, with this report, to share the lessons learned, which show mobility limitations faced by low-income residents and the challenge of transposing social and spatial segregation in large urban centers.

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The R codes provide Bayesian model fitting procedures for AAR-\^{}14\^{}C datasets. These codes are updated versions of the analytical scripts published by Allen et al. (2013). \\ Based on the ages derived from the models fitted, it is possible then to account for the time-averaging (temporal resolution of the fossil record). The time-averaging estimates are based on empirical posterior distributions, accounting for dating uncertainty, as in Ritter et al. (2017).\İn addition, the R codes implements the figures produced both the cited dissertation and its derived manuscripts, like the best models fitted, age-frequency distribuitions (Histograms), its relations with sea-level oscilation in the Southern Brazilian shelf etc.

BACKGROUND: Little evidence is available regarding the effects of long-term periodontal infection on diabetes mellitus (DM) control. The aim of this retrospective cohort study is to evaluate influence of periodontal status on changes of glycated hemoglobin (HbA1c) levels of patients with type 2 DM (DMt2). METHODS: Eighty patients (mean age: 56.0 +/- 8.9 years) with DMt2 were included. Patients were non-smokers, aged >/=40 years, and using antidiabetic drugs. Demographics, health history, and HbA1c levels were retrieved from medical charts. Probing depth and clinical attachment loss (AL) were recorded. RESULTS: Patients were examined at two time points within a mean interval of 38.6 +/- 6.6 months. Increase in HbA1c over time was statistically significant when severe periodontitis was diagnosed at baseline (2.32%, 95% confidence interval [CI]: 1.50% to 3.15%), in patients showing at least one tooth with >/=2 mm of AL progression (2.24%, 95% CI: 1.56% to 2.91%), in males (2.75%, 95% CI: 1.72% to 3.78%), and in those with HbA1c <6.5% at baseline (3.08%, 95% CI: 2.47% to 3.69%). After adjusting for baseline HbA1c, significant changes were still observed for severe periodontitis and progression of AL with increases of 0.85% and 0.9%, respectively. After adjusting for sex and HbA1c, AL progression was also statistically significant, with increases of 0.84%. CONCLUSIONS: Periodontitis progression was associated with increase in HbA1c in patients with DMt2. Identification of these risk factors suggests that periodontal treatment may improve glycemic control of patients with DMt2 by eliminating periodontal infection.

BACKGROUND: The aim of this study is to investigate the impact of alcohol consumption on clinical attachment loss (AL) progression over a period of 5 years. METHODS: A multistage probability sampling strategy was used to draw a representative sample of the metropolitan area of Porto Alegre, Brazil. Five hundred thirty-two individuals (209 males and 293 females) aged 18 to 65 years at baseline with no medical history of diabetes and at least six teeth were included in this analysis. Full-mouth periodontal examinations with six sites per tooth were conducted at baseline and after 5 years. Alcohol consumption was assessed at baseline by asking participants about the usual number of drinks consumed in a week. Four categories of alcohol consumption were defined: 1) non-drinker; 2) 1 glass/week and 1 glass/day. Individuals showing at least two teeth with proximal (clinical AL) progression >/=3 mm over 5 years were classified as having disease progression. Multiple Poisson regression models adjusted for age, sex, smoking, socioeconomic status, and body mass index were used to estimate relative risks (RRs) and 95% confidence intervals (CIs). RESULTS: Overall, individuals who consumed >1 glass/day had 30% higher risk for clinical AL progression (RR = 1.30; 95% CI: 1.07 to 1.58) than non-drinkers. Among males, risk of clinical AL progression for individuals drinking >1 glass/day was 34% higher than non-drinkers (RR = 1.34; 95% CI: 1.09 to 1.64). Never-smoker males drinking 1 glass/day had significantly higher risk (RR = 1.50; 95% CI: 1.08 to 1.99). Among females, no association between alcohol consumption and clinical AL progression was observed. CONCLUSIONS: Alcohol consumption increased the risk of clinical AL progression, and this effect was more pronounced in males. Low dosages (