G. Belarmino
University of São Paulo
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Publication
Featured researches published by G. Belarmino.
World Journal of Hepatology | 2017
G. Belarmino; Maria Cristina Gonzalez; Raquel Susana Torrinhas; Priscila Sala; Wellington Andraus; Luiz Augusto Carneiro D’Albuquerque; Rosa Maria Rodrigues Pereira; V. F. Caparbo; Graziela Rosa Ravacci; Lucas Damiani; Steven B. Heymsfield; Dan Linetzky Waitzberg
AIM To evaluate the prognostic value of the phase angle (PA) obtained from bioelectrical impedance analysis (BIA) for mortality prediction in patients with cirrhosis. METHODS In total, 134 male cirrhotic patients prospectively completed clinical evaluations and nutritional assessment by BIA to obtain PAs during a 36-mo follow-up period. Mortality risk was analyzed by applying the PA cutoff point recently proposed as a malnutrition marker (PA ≤ 4.9°) in Kaplan-Meier curves and multivariate Cox regression models. RESULTS The patients were divided into two groups according to the PA cutoff value (PA > 4.9°, n = 73; PA ≤ 4.9°, n = 61). Weight, height, and body mass index were similar in both groups, but patients with PAs > 4.9° were younger and had higher mid-arm muscle circumference, albumin, and handgrip-strength values and lower severe ascites and encephalopathy incidences, interleukin (IL)-6/IL-10 ratios and C-reactive protein levels than did patients with PAs ≤ 4.9° (P ≤ 0.05). Forty-eight (35.80%) patients died due to cirrhosis, with a median of 18 mo (interquartile range, 3.3-25.6 mo) follow-up until death. Thirty-one (64.60%) of these patients were from the PA ≤ 4.9° group. PA ≤ 4.9° significantly and independently affected the mortality model adjusted for Model for End-Stage Liver Disease score and age (hazard ratio = 2.05, 95%CI: 1.11-3.77, P = 0.021). In addition, Kaplan-Meier curves showed that patients with PAs ≤ 4.9° were significantly more likely to die. CONCLUSION In male patients with cirrhosis, the PA ≤ 4.9° cutoff was associated independently with mortality and identified patients with worse metabolic, nutritional, and disease progression profiles. The PA may be a useful and reliable bedside tool to evaluate prognosis in cirrhosis.
Clinical and translational gastroenterology | 2017
Priscila Sala; G. Belarmino; Raquel Susana Torrinhas; N.M. Machado; Danielle Cristina Fonseca; Graziela Rosa Ravacci; Robson K. Ishida; Ismael Francisco Mota Siqueira Guarda; Eduardo G. de Moura; Paulo Sakai; Marco Aurélio Santo; Ismael D.C.G. Silva; Claudia Pereira; Angela Flavia Logullo; Steven B. Heymsfield; Daniel Giannella-Neto; Dan Linetzky Waitzberg
OBJECTIVES: Vitamin B12 (B12) deficiency after Roux‐en‐Y gastric bypass (RYGB) is highly prevalent and may contribute to postoperative complications. Decreased production of intrinsic factor owing to gastric fundus removal is thought to have a major role, but other components of B12 metabolism may also be affected. We evaluated changes in the expression levels of multiple B12 pathway‐encoding genes in gastrointestinal (GI) tissues to evaluate the potential roles in contributing to post‐RYGB B12 deficiency. METHODS: During double‐balloon enteroscopy, serial GI biopsies were collected from 20 obese women (age, 46.9±6.2 years; body mass index, 46.5±5.3 kg/m2) with adult‐onset type 2 diabetes (fasting plasma glucose ≥126 mg/dl; hemoglobin A1c≥6.5%) before and, at the same site, 3 months after RYGB. Gene expression levels were assessed by the Affymetrix Human GeneChip 1.0 ST microarray. Findings were validated by real‐time quantitative PCR (RT–qPCR). RESULTS: Gene expression levels with significant changes (P≤0.05) included: transcobalamin I (TCN1) in remnant (−1.914‐fold) and excluded (−1.985‐fold) gastric regions; gastric intrinsic factor (GIF) in duodenum (−0.725‐fold); and cubilin (CUBN) in duodenum (+0.982‐fold), jejunum (+1.311‐fold), and ileum (+0.685‐fold). Validation by RT–qPCR confirmed (P≤0.05) observed changes for TCN1 in the remnant gastric region (−0.132‐fold) and CUBN in jejunum (+2.833‐fold). CONCLUSIONS: RYGB affects multiple pathway‐encoding genes that may be associated with postoperative B12 deficiency. Decreased TCN1 levels seem to be the main contributing factor. Increased CUBN levels suggest an adaptive genetic reprogramming of intestinal tissue aiming to compensate for impaired intestinal B12 delivery.
Journal of International Medical Research | 2016
Priscila Sala; G. Belarmino; N.M. Machado; Camila Siqueira Cardinelli; Karina Al Assal; Mariane Marques da Silva; Danielle Cristina Fonseca; Robson K. Ishida; Marco Aurélio Santo; Eduardo Guimarães Hourneaux de Moura; Paulo Sakai; Ismael Francisco Mota Siqueira Guarda; Ismael Dale Cotrim Guerreiro da Silva; Agatha Sacramento Rodrigues; Carlos Alberto Pereira; Steven B. Heymsfield; Joël Doré; Raquel Susana Torrinhas; Daniel Giannella-Neto; Dan Linetzky Waitzberg
Objective To describe the protocol of the SURgically induced Metabolic effects on the Human GastroIntestinal Tract (SURMetaGIT) study, a clinical pan-omics study exploring the gastrointestinal tract as a central organ driving remission of type 2 diabetes mellitus (T2DM) after Roux-en-Y gastric bypass (RYGB). The main points considered in the study’s design and challenges faced in its application are detailed. Methods This observational, longitudinal, prospective study involved collection of gastrointestinal biopsy specimens, faeces, urine, and blood from 25 obese women with T2DM who were candidates for RYGB (20 patients for omics assessment and 5 for omics validation). These collections were performed preoperatively and 3 and 24 months postoperatively. Gastrointestinal transcriptomics; faecal metagenomics and metabolomics; plasma proteomics, lipidomics, and metabolomics; and biochemical, nutritional, and metabolic data were assessed to identify their short- and long-term correlations with T2DM remission. Results Data were collected from 20 patients before and 3 months after RYGB. These patients have nearly completed the 2-year follow-up assessments. The five additional patients are currently being selected for omics data validation. Conclusion The multi-integrated pan-omics approach of the SURMetaGIT study enables integrated analysis of data that will contribute to the understanding of molecular mechanisms involved in T2DM remission after RYGB.
Journal of Parenteral and Enteral Nutrition | 2017
G. Belarmino; M.C. Gonzalez; Priscila Sala; Raquel Susana Torrinhas; Wellington Andraus; Luiz Augusto Carneiro D’Albuquerque; Rosa Maria Rodrigues Pereira; V. F. Caparbo; Eduardo Ferrioli; Karina Pfrimer; Lucas Damiani; Steven B. Heymsfield; Dan Linetzky Waitzberg
BACKGROUND Ascites in cirrhotic patients interfere with accurate assessment of skeletal muscle when diagnosing sarcopenia. We hypothesized measurement of appendicular skeletal muscle index (ASMI) with dual-energy x-ray absorptiometry (DXA) improves the diagnosis of sarcopenia in cirrhotic patients as ASMI does not include the fluid-filled abdominal compartment. OBJECTIVE To evaluate if ASMI is influenced by ascites, lower limb edema (LLE) and predicts mortality alone or combined with handgrip strength (HGS) in cirrhotic patients. DESIGN ASMI, HGS, and 36-month mortality were obtained in 144 men with cirrhosis. ASMI was compared before and after paracentesis in 20 men with ascites and to results from 20 matched controls. The prognostic value of ASMI alone and with HGS was tested in a survival. Survival probabilities were obtained for sarcopenia diagnosed by standard ASMI and HGS European Working Group on Sarcopenia in Older People (EWGSOP) cutoffs and a new cutoff calculated from our ASMI + HGS tertiles. RESULTS ASMI did not change after paracentesis, was lower in patients than in controls (P < .001), and was not influenced by LLE (D = 0.30 kg/m2, P = .068; R2 = 2.40%). Mortality was influenced by ASMI and HGS (Pinteraction = 0.028). Sarcopenia diagnosed by EWGSOP was also diagnosed by our new cutoff; both predicted mortality with the latter more sensitive for mortality risk prediction (P = .011). CONCLUSIONS DXA-measured ASMI is not influenced by ascites or LLE in cirrhotic patients; can diagnose low skeletal muscle/sarcopenia; and predicts mortality, particularly when combined with HGS.
BMC Obesity | 2018
G. Belarmino; Raquel Susana Torrinhas; Priscila Sala; Lilian Mika Horie; Lucas Damiani; Natalia C. Lopes; Steven B. Heymsfield; Dan Linetzky Waitzberg
BackgroundBody mass index (BMI) has been used to assess body adiposity, but it cannot adequately reflect body fat (BF) amount. The body adiposity index (BAI) has been shown a better performance than BMI for this purpose, but it can be inaccurate to estimate BF under extreme amounts of fat. Here, we propose a new anthropometric index, the Belarmino–Waitzberg (BeW) index, for specific estimation of BF in severely obese patients.MethodsIn 144 adult patients with severe obesity, BF was estimated by air displacement plethysmography (ADP), as the reference method, along with the follow anthropometric measurements: height, abdominal circumference (AC), hip circumference (HC), weight, BMI (weight/ height2) and BAI ([HC(cm) / height (m)1.5) − 18] × 100). Patients were proportionately distributed into two distinct databases, the building model database (BMD) and the validation model database (VMD), which were applied to develop and validate the BeW index, respectively. The BeW index was tested for gender and ethnicity adjustment as independent variables. The agreement of BF% values obtained by the new index and by BAI with ADP was also assessed.ResultsThe BF% was 52.05 ± 5.42 for ADP and 59.11 ± 5.95 for the BeW index (all results are expressed as the mean ± standard deviation). A positive Pearson correlation (r = 0.74), a good accuracy (Cb = 0.94), and a positive Lin’s concordance correlation (CCC = 0.70) were observed between the two groups. The 95% limits of individual agreement between the BeW index and ADP were 6.8 to 7.9%, compared to − 7.5 to 14.8% between the BAI and ADP. The new index, called the Belarmino–Waitzberg (BeW) index, showed an improvement of 2.1% for the R2 value and a significant gender effect, therefore resulting in two different indexes for females and males, as follows: Female BeW = − 48.8 + 0.087 × AC(cm) + 1.147 × HC(cm) - 0.003 × HC(cm)2 and Male BeW = − 48.8 + 0.087 × AC(cm) + 1.147 × HC(cm) - 0.003 × HC(cm)2–7.195.ConclusionsThe new BeW index showed a good performance for BF estimation in patients with severe obesity and can be superior to the BAI for this purpose.
Nutrition Journal | 2015
G. Belarmino; Lilian Mika Horie; Priscila Sala; Raquel Susana Torrinhas; Steven B. Heymsfield; Dan Linetzky Waitzberg
Clinical Nutrition | 2018
Priscila Garla; Priscila Sala; Raquel Susana Torrinhas; N.M. Machado; Danielle Cristina Fonseca; Mariane Marques da Silva; Graziela Rosa Ravacci; G. Belarmino; Robson K. Ishida; Ismael Francisco Mota Siqueira Guarda; Eduardo Guimarães Hourneaux de Moura; Paulo Sakai; Marco Aurélio Santo; Ismael Dale Cotrim Guerreiro da Silva; Claudia Pereira; Steven B. Heymsfield; Maria Lúcia Corrêa-Giannella; Philip C. Calder; Dan Linetzky Waitzberg
Clinical Nutrition | 2018
G. Belarmino; Pierre Singer; M.C. Gonzalez; N.M. Machado; C.S. Cardinelli; S. Barcelos; Wellington Andraus; L.A.C. D'Albuquerque; L. Damiani; A.C. Costa; Rosa Maria Rodrigues Pereira; Steven B. Heymsfield; Priscila Sala; R.S. Torrinhas; Dan Linetzky Waitzberg
Clinical Nutrition | 2017
G. Belarmino; M.C. Gonzalez; R.S. Torrinhas; Wellington Andraus; L.A.C. D’Albuquerque; L. Damiani; Priscila Sala; Steven B. Heymsfield; Dan Linetzky Waitzberg
Journal of Advanced Nutrition and Human Metabolism | 2016
G. Belarmino; Priscila Sala; Raquel Sm Torrinhas; Dan Linetzky Waitzberg