Renato G B Bandeira de Mello

Prof. Renato G B Bandeira de Mello


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 February 2016 in BMJ Open
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Journal Article
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ASAndressa Alves da Silva
Andressa Alves da Silva
RMRenato G B Bandeira de Mello
Renato G B Bandeira de Mello
CSCamila Wohlgemuth Schaan
Camila Wohlgemuth Schaan
FFFlávio Danni Fuchs
Flávio Danni Fuchs
SRSusan Redline
Susan Redline
SFSandra Fuchs
Sandra Fuchs
Objective: The purpose of our study was to evaluate the association between short and long sleep duration and all-cause and cardiovascular mortality among elderly individuals. Design: Systematic review and meta-analysis of population-based cohort studies. Setting: Articles were retrieved from international and national electronic databases. Study selection: Studies were identified in PubMed, EMBASE, LILACS (Latin American and Caribbean Health Sciences Literature), IBECS (Bibliographic Index on Health Sciences from Spain) and CAPES (PhD thesis repository) between 1980 and 2015. Studies which met all criteria were eligible: participants aged 60 years or over, assessment of sleep duration as 24 h, nighttime or daytime sleep, evaluation of all-cause or cause-specific mortality, population-based cohort studies conducted on representative samples. There was no language restriction and studies published as abstracts were excluded. Data extraction: Data were analysed using the Comprehensive Meta-Analysis software (V.3.3.070), and summary estimates (relative risk (RR), 95% CI) were calculated using a random effects model. Heterogeneity and consistency were evaluated through Cochran's Q and the I 2 statistics, respectively, and sensitivity analyses were conducted. Primary and secondary outcome measures: All-cause and cardiovascular mortality. Results: Overall, 27 cohort studies were selected, comprising >70 000 elderly individuals, and followed up from 3.4 to 35 years. In the pooled analysis, long and short sleep duration were associated with increased all-cause mortality (RR 1.33; 95% CI 1.24 to 1.43 and RR 1.07; 95% CI 1.03 to 1.11, respectively), compared with the reference category. For cardiovascular mortality, the pooled relative risks were 1.43 (95% CI 1.15 to 1.78) for long sleep, and 1.18 (95% CI 0.76 to 1.84) for short sleep. Daytime napping ≥30 min was associated with risk of all-cause mortality (RR 1.27; 95% CI 1.08 to 1.49), compared with no daytime sleep, but longer sleep duration (≥2.0 h) was not (RR 1.34; 95% CI 1.95 to 1.90). Conclusions: Among elderly individuals, long and short sleep duration are associated with increased risk for all-cause mortality. Long sleep duration is associated with cardiovascular mortality.

20 November 2019 in Journal of Aging Research
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RMRenato G B Bandeira de Mello
Renato G B Bandeira de Mello
RCRoberta Rigo Dalla Corte
Roberta Rigo Dalla Corte
JGJoana Gioscia
Joana Gioscia
EMEmilio Hideyuki Moriguchi
Emilio Hideyuki Moriguchi
Introduction. Sarcopenia is a prevalent condition in the elderly population, imposing a significant impact over their functional ability as well as their quality of life. Furthermore, it is associated with greater incidence of major geriatric outcomes, as reduced mobility, falls, loss of independence, cognitive impairment, and all-cause mortality. Physical Exercise Programs directed to improve muscle mass and its function may be key to reduce sarcopenia consequences. However, a significant heterogeneity is found in clinical trials, especially as a consequence of different exercise protocols applied to research subjects. Objectives. To access the effects of physical exercise programs compared to no exercise interventions to improve sarcopenia components and its determinants in sarcopenic elder individuals. Methods. A systematic review was conducted in the Pubmed database to identify randomized clinical trials (RCTs) which tested the effects of physical exercise programs to manage sarcopenia components in sarcopenic elder individuals. Two independent reviewers assessed the studies’ eligibility according to specified inclusion criteria in a four-step strategy. Data regarding population characteristics, muscle mass, muscle quality, muscle strength, and muscle function were extracted from each one of the included studies. Assessment of quality and individual studies risk of bias were assessed through Cochrane Risk of Bias Tool®. Assuming theoretical expected heterogeneity among studies, especially regarding different physical exercise programs and different outcome measurements, authors decided to be conservative and present study results in descriptive tables. Results. Search strategy retrieved 298 papers on PubMed database. Three more were identified through manual search, being 301 studies revised for inclusion. 278 were excluded during title/abstract review. After further evaluation of 23 full-texts, 5 RCTs were included. All 5 trials tested the efficacy of isolated exercise programs to improve sarcopenia components in the elderly compared to no physical intervention. Resistance training was the main intervention component in all included trials compared to inactive control groups (health education mainly). Physical training improved muscle strength, muscle quality, and muscle function compared to inactive control groups. Considering muscle mass, no differences were demonstrated. Data meta-analysis was not possible to be performed due to high heterogeneity among trials and small number of studies for each outcome comparison. Conclusion. Heterogeneity among trials and small number of RCTs limited robust conclusions and data meta-analysis. However, resistance training protocols can improve muscle strength and physical performance in elders previously diagnosed with sarcopenia, although its effect size and clinical impact are barely relevant.

1 December 2016 in Journal of the American Heart Association
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Journal Article
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SFSandra Fuchs
Sandra Fuchs
CPCarlos E. Poli‐De‐Figueiredo
Carlos E. Poli‐De‐Figueiredo
JNJosé A. Figueiredo Neto
José A. Figueiredo Neto
LSLuiz César N. Scala
Luiz César N. Scala
PWPaul K. Whelton
Paul K. Whelton
FFFlávio Danni Fuchs
Flávio Danni Fuchs
Background: Prehypertension is associated with higher cardiovascular risk, target organ damage, and incidence of hypertension. The Prevention of Hypertension in Patients with PreHypertension (PREVER‐Prevention) trial aimed to evaluate the efficacy and safety of a low‐dose diuretic for the prevention of hypertension and end‐organ damage. Methods and Results: This randomized, parallel, double‐blind, placebo‐controlled trial was conducted in 21 Brazilian academic medical centers. Participants with prehypertension who were aged 30 to 70 years and who did not reach optimal blood pressure after 3 months of lifestyle intervention were randomized to a chlorthalidone/amiloride combination pill or placebo and were evaluated every 3 months during 18 months of treatment. The primary outcome was incidence of hypertension. Development or worsening of microalbuminuria, new‐onset diabetes mellitus, and reduction of left ventricular mass were secondary outcomes. Participant characteristics were evenly distributed by trial arms. The incidence of hypertension was significantly lower in 372 study participants allocated to diuretics compared with 358 allocated to placebo (hazard ratio 0.56, 95% CI 0.38–0.82), resulting in a cumulative incidence of 11.7% in the diuretic arm versus 19.5% in the placebo arm ( P =0.004). Adverse events; levels of blood glucose, glycosylated hemoglobin, creatinine, and microalbuminuria; and incidence of diabetes mellitus were no different between the 2 arms. Left ventricular mass assessed through Sokolow‐Lyon voltage and voltage‐duration product decreased to a greater extent in participants allocated to diuretic therapy compared with placebo ( P =0.02). Conclusions: A combination of low‐dose chlorthalidone and amiloride effectively reduces the risk of incident hypertension and beneficially affects left ventricular mass in patients with prehypertension. Clinical Trial Registration: URL : http://www.ClinicalTrials.gov , www.ensaiosclinicos.gov . Unique identifiers: NCT 00970931, RBR ‐74rr6s.

9 August 2024 in Nature Aging
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PBPhilipe De Souto Barreto
Philipe De Souto Barreto
EGEmmanuel Gonzalez-Bautista
Emmanuel Gonzalez-Bautista
HBHeike A. Bischoff-Ferrari
Heike A. Bischoff-Ferrari
VOVitor Pelegrim de Oliveira
Vitor Pelegrim de Oliveira
RMRenato G B Bandeira de Mello
Renato G B Bandeira de Mello
BVBruno Vellas
Bruno Vellas


28 July 2023 in Maturitas
Verified
Journal Article
Closed access
VOVitor Pelegrim de Oliveira
Vitor Pelegrim de Oliveira
EFEduardo Ferriolli
Eduardo Ferriolli
RLRoberto Alves Lourenço
Roberto Alves Lourenço
EGEmmanuel Gonzalez-Bautista
Emmanuel Gonzalez-Bautista
PBPhilipe De Souto Barreto
Philipe De Souto Barreto
RMRenato G B Bandeira de Mello
Renato G B Bandeira de Mello