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Renan P. Souza

Bio: Renan P. Souza is an academic researcher from Universidade Federal de Minas Gerais. The author has contributed to research in topics: Schizophrenia & Antipsychotic. The author has an hindex of 23, co-authored 102 publications receiving 2059 citations. Previous affiliations of Renan P. Souza include Faculdade de Medicina da Universidade Federal de Minas Gerais & Universidade do Extremo Sul Catarinense.


Papers
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Journal ArticleDOI
Darlan da Silva Candido1, Darlan da Silva Candido2, Ingra Morales Claro1, Jaqueline Goes de Jesus1, William Marciel de Souza, Filipe R. R. Moreira3, Simon Dellicour4, Simon Dellicour5, Thomas A. Mellan6, Louis du Plessis2, Rafael Henrique Moraes Pereira, Flavia C. S. Sales1, Erika R. Manuli1, Julien Thézé7, Luiz Carlos de Almeida, Mariane Talon de Menezes3, Carolina M. Voloch3, Marcílio Jorge Fumagalli, Thais M. Coletti1, Camila A. M. Silva1, Mariana S. Ramundo1, Mariene R. Amorim8, Henrique Hoeltgebaum6, Swapnil Mishra6, Mandev S. Gill5, Luiz Max Carvalho9, Lewis F Buss1, Carlos A. Prete1, Jordan Ashworth10, Helder I. Nakaya1, Pedro S. Peixoto1, Oliver J. Brady11, Samuel M. Nicholls12, Amilcar Tanuri3, Átila Duque Rossi3, Carlos Kaue Vieira Braga, Alexandra L. Gerber, Ana Paula de C Guimarães, Nelson Gaburo, Cecila Salete Alencar1, Alessandro C. S. Ferreira, Cristiano Xavier Lima13, José Eduardo Levi14, Celso Francisco Hernandes Granato, Giulia M. Ferreira15, Ronaldo da Silva Francisco, Fabiana Granja8, Fabiana Granja16, Márcia Teixeira Garcia8, Maria Luiza Moretti8, Mauricio W. Perroud8, Terezinha M. P. P. Castineiras3, Carolina S. Lazari1, Sarah C. Hill17, Sarah C. Hill2, Andreza Aruska de Souza Santos2, Camila L. Simeoni8, Julia Forato8, Andrei C. Sposito8, Angelica Zaninelli Schreiber8, Magnun N. N. Santos8, Camila Zolini de Sá13, Renan P. Souza13, Luciana C. Resende-Moreira13, Mauro M. Teixeira13, Josy Hubner13, Patricia Asfora Falabella Leme8, Rennan G. Moreira13, Maurício Lacerda Nogueira18, Neil M. Ferguson1, Silvia Figueiredo Costa8, José Luiz Proença-Módena, Ana Tereza Ribeiro de Vasconcelos6, Samir Bhatt5, Philippe Lemey19, Chieh-Hsi Wu10, Andrew Rambaut12, Nicholas J. Loman13, Renato Santana Aguiar2, Oliver G. Pybus1, Ester Cerdeira Sabino2, Ester Cerdeira Sabino1, Ester Cerdeira Sabino6, Nuno R. Faria6, Nuno R. Faria2, Nuno R. Faria1 
23 Jul 2020-Science
TL;DR: New light is shed on the epidemic transmission and evolutionary trajectories of SARS-CoV-2 lineages in Brazil and evidence that current interventions remain insufficient to keep virus transmission under control in this country is provided.
Abstract: Brazil currently has one of the fastest-growing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) epidemics in the world. Because of limited available data, assessments of the impact of nonpharmaceutical interventions (NPIs) on this virus spread remain challenging. Using a mobility-driven transmission model, we show that NPIs reduced the reproduction number from >3 to 1 to 1.6 in Sao Paulo and Rio de Janeiro. Sequencing of 427 new genomes and analysis of a geographically representative genomic dataset identified >100 international virus introductions in Brazil. We estimate that most (76%) of the Brazilian strains fell in three clades that were introduced from Europe between 22 February and 11 March 2020. During the early epidemic phase, we found that SARS-CoV-2 spread mostly locally and within state borders. After this period, despite sharp decreases in air travel, we estimated multiple exportations from large urban centers that coincided with a 25% increase in average traveled distances in national flights. This study sheds new light on the epidemic transmission and evolutionary trajectories of SARS-CoV-2 lineages in Brazil and provides evidence that current interventions remain insufficient to keep virus transmission under control in this country.

286 citations

DOI
Darlan da Silva Candido, Ingra Morales Claro, Jaqueline Goes de Jesus, William Marciel de Souza, Filipe R. R. Moreira, Simon Dellicour, Thomas A. Mellan, Louis du Plessis, Rafael Henrique Moraes Pereira, Flavia C. S. Sales, Erika R. Manuli, Julien Thézé, Luiz Carlos de Almeida, Mariane Talon de Menezes, Carolina M. Voloch, Marcílio Jorge Fumagalli, Thais M. Coletti, Camila A. M. Silva, Mariana S. Ramundo, Mariene R. Amorim, Henrique Hoeltgebaum, Swapnil Mishra, Mandev S. Gill, Luiz Max Carvalho, Lewis F Buss, Carlos A. Prete, Jordan Ashworth, Helder I. Nakaya, Pedro S. Peixoto, Oliver J. Brady, Samuel M. Nicholls, Amilcar Tanuri, Átila Duque Rossi, Carlos Kaue Vieira Braga, Alexandra L. Gerber, Ana Paula de C Guimarães, Nelson Gaburo, Cecila Salete Alencar, Alessandro C. S. Ferreira, Cristiano Xavier Lima, José Eduardo Levi, Celso Francisco Hernandes Granato, Giulia M. Ferreira, Ronaldo da Silva Francisco, Fabiana Granja, Márcia Teixeira Garcia, Maria Luiza Moretti, Mauricio W. Perroud, Terezinha M. P. P. Castineiras, Carolina S. Lazari, Sarah C. Hill, Andreza Aruska de Souza Santos, Camila L. Simeoni, Julia Forato, Andrei C. Sposito, Angelica Zaninelli Schreiber, Magnun N. N. Santos, Camila Zolini de Sá, Renan P. Souza, Luciana C. Resende-Moreira, Mauro M. Teixeira, Josy Hubner, Patricia Asfora Falabella Leme, Rennan G. Moreira, Maurício Lacerda Nogueira, Neil M. Ferguson, Silvia Figueiredo Costa, José Luiz Proença-Módena, Ana Tereza Ribeiro de Vasconcelos, Samir Bhatt, Philippe Lemey, Chieh-Hsi Wu, Andrew Rambaut, Nicholas J. Loman, Renato Santana Aguiar, Oliver G. Pybus, Ester Cerdeira Sabino, Nuno R. Faria 
05 Aug 2020
TL;DR: New light is shed on the epidemic transmission and evolutionary trajectories of SARS-CoV-2 lineages in Brazil, and evidence that current interventions remain insufficient to keep virus transmission under control in the country is provided.
Abstract: Brazil currently has one of the fastest growing SARS-CoV-2 epidemics in the world. Owing to limited available data, assessments of the impact of non-pharmaceutical interventions (NPIs) on virus spread remain challenging. Using a mobility-driven transmission model, we show that NPIs reduced the reproduction number from >3 to 1–1.6 in Sao Paulo and Rio de Janeiro. Sequencing of 427 new genomes and analysis of a geographically representative genomic dataset identified >100 international virus introductions in Brazil. We estimate that most (76%) of the Brazilian strains fell in three clades that were introduced from Europe between 22 February11 March 2020. During the early epidemic phase, we found that SARS-CoV-2 spread mostly locally and within-state borders. After this period, despite sharp decreases in air travel, we estimated multiple exportations from large urban centers that coincided with a 25% increase in average travelled distances in national flights. This study sheds new light on the epidemic transmission and evolutionary trajectories of SARS-CoV-2 lineages in Brazil, and provide evidence that current interventions remain insufficient to keep virus transmission under control in the country.

138 citations

Journal ArticleDOI
TL;DR: It is found that none of the single polymorphisms investigated on DRD1 and DRD3 were associated with CPGI scores in healthy subjects, and the role of dopamine D2-like receptor in addiction susceptibility is provided.

111 citations

Journal ArticleDOI
TL;DR: An updated meta-analysis of nine previous studies plus the current sample suggest that the -759C allele is associated with antipsychotic-induced weight gain.
Abstract: Aims: This study aims to test for possible associations between the gene coding for the 5-HT2C receptor and antipsychotic-induced weight gain. Materials & methods: Four HTR2C polymorphisms (rs498207, C-759T, G-697C and Ser23Cys) were investigated in our sample of 205 chronic schizophrenia patients. Results: Significant over-representation of the C–G–Cys23 haplotype in patients with weight gain (OR: 1.93; 95% CI: 1.04–3.56; p = 0.0015) was found. Similarly, haplotype analyses of percentage weight change were also significant (p = 0.029) for the C–G–Cys23 haplotype associated with the highest average percent weight gain. Observations in the polymorphisms are consistent with previous studies. An updated meta-analysis of nine previous studies plus our current sample suggest that the -759C allele is associated with antipsychotic-induced weight gain. Conclusion: Additional studies, including the resequencing of the region surrounding the HTR2C promoter, and functional studies of the promoter polymorphisms, may ...

103 citations

Journal ArticleDOI
TL;DR: Evidence is provided that the CNR1 gene may be associated with antipsychotic-induced weight gain in chronic schizophrenia patients and electrophoretic mobility shift assays showed that the presence of the T allele created a binding site for arylhydrocarbon receptor translocator (ARNT), a member of the basic helix–loop–helix/Per–Arnt–Sim protein family.

97 citations


Cited by
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Journal ArticleDOI
TL;DR: D dopamine receptor classification, their basic structural and genetic organization, their distribution and functions in the brain and the periphery, and their regulation and signal transduction mechanisms are discussed.
Abstract: G protein-coupled dopamine receptors (D1, D2, D3, D4, and D5) mediate all of the physiological functions of the catecholaminergic neurotransmitter dopamine, ranging from voluntary movement and reward to hormonal regulation and hypertension. Pharmacological agents targeting dopaminergic neurotransmission have been clinically used in the management of several neurological and psychiatric disorders, including Parkinson's disease, schizophrenia, bipolar disorder, Huntington's disease, attention deficit hyperactivity disorder (ADHD(1)), and Tourette's syndrome. Numerous advances have occurred in understanding the general structural, biochemical, and functional properties of dopamine receptors that have led to the development of multiple pharmacologically active compounds that directly target dopamine receptors, such as antiparkinson drugs and antipsychotics. Recent progress in understanding the complex biology of dopamine receptor-related signal transduction mechanisms has revealed that, in addition to their primary action on cAMP-mediated signaling, dopamine receptors can act through diverse signaling mechanisms that involve alternative G protein coupling or through G protein-independent mechanisms via interactions with ion channels or proteins that are characteristically implicated in receptor desensitization, such as β-arrestins. One of the future directions in managing dopamine-related pathologic conditions may involve a transition from the approaches that directly affect receptor function to a precise targeting of postreceptor intracellular signaling modalities either directly or through ligand-biased signaling pharmacology. In this comprehensive review, we discuss dopamine receptor classification, their basic structural and genetic organization, their distribution and functions in the brain and the periphery, and their regulation and signal transduction mechanisms. In addition, we discuss the abnormalities of dopamine receptor expression, function, and signaling that are documented in human disorders and the current pharmacology and emerging trends in the development of novel therapeutic agents that act at dopamine receptors and/or on related signaling events.

2,259 citations

21 Jun 2010

1,966 citations

Journal ArticleDOI
TL;DR: The American Heart Association, through its Statistics Committee, continuously monitors and evaluates sources of data on heart disease and stroke in the United States to provide the most current information available in the annual Statistical Update as discussed by the authors .
Abstract: The American Heart Association, in conjunction with the National Institutes of Health, annually reports the most up-to-date statistics related to heart disease, stroke, and cardiovascular risk factors, including core health behaviors (smoking, physical activity, diet, and weight) and health factors (cholesterol, blood pressure, and glucose control) that contribute to cardiovascular health. The Statistical Update presents the latest data on a range of major clinical heart and circulatory disease conditions (including stroke, congenital heart disease, rhythm disorders, subclinical atherosclerosis, coronary heart disease, heart failure, valvular disease, venous disease, and peripheral artery disease) and the associated outcomes (including quality of care, procedures, and economic costs).The American Heart Association, through its Statistics Committee, continuously monitors and evaluates sources of data on heart disease and stroke in the United States to provide the most current information available in the annual Statistical Update. The 2022 Statistical Update is the product of a full year's worth of effort by dedicated volunteer clinicians and scientists, committed government professionals, and American Heart Association staff members. This year's edition includes data on the monitoring and benefits of cardiovascular health in the population and an enhanced focus on social determinants of health, adverse pregnancy outcomes, vascular contributions to brain health, and the global burden of cardiovascular disease and healthy life expectancy.Each of the chapters in the Statistical Update focuses on a different topic related to heart disease and stroke statistics.The Statistical Update represents a critical resource for the lay public, policymakers, media professionals, clinicians, health care administrators, researchers, health advocates, and others seeking the best available data on these factors and conditions.

1,483 citations

Journal ArticleDOI
Nuno R. Faria, Thomas A. Mellan1, Charles Whittaker1, Ingra Morales Claro2, Darlan da Silva Candido3, Darlan da Silva Candido2, Swapnil Mishra1, Myuki A E Crispim, Flavia C. S. Sales2, Iwona Hawryluk1, John T. McCrone4, Ruben J.G. Hulswit3, Lucas A M Franco2, Mariana S. Ramundo2, Jaqueline Goes de Jesus2, Pamela S Andrade2, Thais M. Coletti2, Giulia M. Ferreira5, Camila A. M. Silva2, Erika R. Manuli2, Rafael Henrique Moraes Pereira, Pedro S. Peixoto2, Moritz U. G. Kraemer3, Nelson Gaburo, Cecilia da C. Camilo, Henrique Hoeltgebaum1, William Marciel de Souza2, Esmenia C. Rocha2, Leandro Marques de Souza2, Mariana C. Pinho2, Leonardo José Tadeu de Araújo6, Frederico S V Malta, Aline B. de Lima, Joice do P. Silva, Danielle A G Zauli, Alessandro C. S. Ferreira, Ricardo P Schnekenberg3, Daniel J Laydon1, Patrick G T Walker1, Hannah M. Schlüter1, Ana L. P. dos Santos, Maria S. Vidal, Valentina S. Del Caro, Rosinaldo M. F. Filho, Helem M. dos Santos, Renato Santana Aguiar7, José Luiz Proença-Módena8, Bruce Walker Nelson9, James A. Hay10, Melodie Monod1, Xenia Miscouridou1, Helen Coupland1, Raphael Sonabend1, Michaela A. C. Vollmer1, Axel Gandy1, Carlos A. Prete2, Vitor H. Nascimento2, Marc A. Suchard11, Thomas A. Bowden3, Sergei L Kosakovsky Pond12, Chieh-Hsi Wu13, Oliver Ratmann1, Neil M. Ferguson1, Christopher Dye3, Nicholas J. Loman14, Philippe Lemey15, Andrew Rambaut4, Nelson Abrahim Fraiji, Maria Perpétuo Socorro Sampaio Carvalho, Oliver G. Pybus3, Oliver G. Pybus16, Seth Flaxman1, Samir Bhatt17, Samir Bhatt1, Ester Cerdeira Sabino2 
21 May 2021-Science
TL;DR: In this article, the authors used a two-category dynamical model that integrates genomic and mortality data to estimate that P.1 may be 1.7-to 2.4-fold more transmissible and that previous (non-P.1) infection provides 54 to 79% of the protection against infection with P.
Abstract: Cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in Manaus, Brazil, resurged in late 2020 despite previously high levels of infection. Genome sequencing of viruses sampled in Manaus between November 2020 and January 2021 revealed the emergence and circulation of a novel SARS-CoV-2 variant of concern. Lineage P.1 acquired 17 mutations, including a trio in the spike protein (K417T, E484K, and N501Y) associated with increased binding to the human ACE2 (angiotensin-converting enzyme 2) receptor. Molecular clock analysis shows that P.1 emergence occurred around mid-November 2020 and was preceded by a period of faster molecular evolution. Using a two-category dynamical model that integrates genomic and mortality data, we estimate that P.1 may be 1.7- to 2.4-fold more transmissible and that previous (non-P.1) infection provides 54 to 79% of the protection against infection with P.1 that it provides against non-P.1 lineages. Enhanced global genomic surveillance of variants of concern, which may exhibit increased transmissibility and/or immune evasion, is critical to accelerate pandemic responsiveness.

985 citations