Maria Teresa Vieira Sanseverino

Dr. Maria Teresa Vieira Sanseverino

orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

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

Representative Publications

View All Publications
1 January 2021 in Epidemiologia e Serviços de Saúde
Verified
Journal Article
Open access
ACAugusto César Cardoso-Dos-Santos
Augusto César Cardoso-Dos-Santos
AMAna Cláudia Medeiros-De-Souza
Ana Cláudia Medeiros-De-Souza
JBJoão Matheus Bremm
João Matheus Bremm
RARonaldo Fernandes Santos Alves
Ronaldo Fernandes Santos Alves
VAValdelaine Etelvina Miranda de Araújo
Valdelaine Etelvina Miranda de Araújo
GFGiovanny Vinícius Araújo de França
Giovanny Vinícius Araújo de França
Resumo Objetivo Definir a lista de anomalias congênitas prioritárias para o aprimoramento do registro no Sistema de Informações sobre Nascidos Vivos (Sinasc). Métodos A partir da Décima Revisão da Classificação Estatística Internacional de Doenças e Problemas Relacionados à Saúde (CID-10), protocolos internacionais e reuniões com especialistas, a lista de anomalias prioritárias foi construída considerando-se dois critérios principais: ser diagnosticável ao nascimento; e possuir intervenção disponível em diferentes níveis. A lista foi submetida a apreciação da Sociedade Brasileira de Genética Médica e Genômica. Resultados Compuseram a lista oito grupos de anomalias congênitas distribuídos de acordo com o tipo de anomalia relacionada, bem como a parte do corpo afetada e sua correspondência ao código do capítulo XVII da CID-10. Conclusão A lista de anomalias congênitas prioritárias para notificação fornece subsídios para o aprimoramento do registro no Sinasc.

11 March 2025 in Viruses
Verified
Journal Article
Open access
PDF file
BRBethania de Freitas Rodrigues Ribeiro
Bethania de Freitas Rodrigues Ribeiro
ABAndré Rodrigues Façanha Barreto
André Rodrigues Façanha Barreto
APAndré Luiz Santos Pessoa
André Luiz Santos Pessoa
RARaimunda Azevedo
Raimunda Azevedo
FRFlávia de Freitas Rodrigues
Flávia de Freitas Rodrigues
LSLavinia Schuler-Faccini
Lavinia Schuler-Faccini
Oropouche fever is caused by the Oropouche virus (OROV; Bunyaviridae, Orthobunyavirus), one of the most frequent arboviruses that infect humans in the Brazilian Amazon. This year, an OROV outbreak was identified in Brazil, and its vertical transmission was reported, which was associated with fetal death and microcephaly. We describe the clinical manifestations identified in three cases of congenital OROV infection with confirmed serology (OROV-IgM) in the mother-newborn binomial. One of the newborns died, and post-mortem molecular analysis using real-time RT-qPCR identified the OROV genome in several tissues. All three newborns were born in the Amazon region in Brazil, and the mothers reported fever, rash, headache, myalgia, and/or retro-orbital pain during pregnancy. The newborns presented with severe microcephaly secondary to brain damage and arthrogryposis, suggestive of an embryo/fetal disruptive process at birth. Brain and spinal images identified overlapping sutures, cerebral atrophy, brain cysts, thinning of the spinal cord, corpus callosum, and posterior fossa abnormalities. Fundoscopic findings included macular chorioretinal scars, focal pigment mottling, and vascular attenuation. The clinical presentation of vertical OROV infection resembled congenital Zika syndrome to some extent but presents some distinctive features on brain imaging and in several aspects of its neurological presentation. A recognizable syndrome with severe brain damage, neurological alterations, arthrogryposis, and fundoscopic abnormalities can be associated with in utero OROV infection.

22 August 2017 in Reproduction, Fertility and Development
Verified
Journal Article
Closed access
PDF file
MFMarcela Felix Fortis
Marcela Felix Fortis
LFLucas Rosa Fraga
Lucas Rosa Fraga
Juliano André BoquettJuliano André Boquett
Juliano André Boquett
TKThayne Kowalski
Thayne Kowalski
CDCaroline Gross Dutra
Caroline Gross Dutra
MSMaria Teresa Vieira Sanseverino
Maria Teresa Vieira Sanseverino
Recurrent pregnancy loss (RPL) affects ~3–5% of couples attempting to conceive and in around 50% of cases the aetiology remains unknown. Adequate vascularisation and placental circulation are indispensable for the development of a normal pregnancy. Prostaglandin-endoperoxide synthase 2 (PTGS2), vascular endothelial growth factor (VEGF) and the nitric oxide (NO) systems play important roles in reproductive physiology, participating in several steps including implantation and apoptosis of trophoblast cells. In this study we evaluated genetic polymorphisms in the inducible nitric oxide synthase (NOS2), PTGS2 and VEGFA genes as susceptibility factors for RPL. A case-control study was conducted in 149 women having two or more miscarriages and 208 controls. Allele and genotype distributions of the polymorphisms studied in the two groups were not statistically different. However, the dominant model showed that the presence of variant T (TT/GT) of rs2779249 (-1290G > T) of NOS2 was significantly associated with RPL (OR = 1.58, CI 95% = 1.03–2.44; P = 0.037). The increased risk remained significant when adjusted for number of pregnancies, alcohol consumption and ethnicity (OR = 1.92, CI95% = 1.18–3.11; P = 0.008). These results suggest that the variant genotypes of the functional polymorphism rs2779249 in the NOS2 promoter are a potential risk for RPL, possibly due to oxidative stress mechanisms.

25 April 2015 in American Journal of Medical Genetics Part A
Verified
Journal Article
Closed access
PDF file
EMEduardo P. Mattos
Eduardo P. Mattos
ASAndré Anjos da Silva
André Anjos da Silva
JMJosé Antônio A Magalhães
José Antônio A Magalhães
JLJúlio César L. Leite
Júlio César L. Leite
SLSandra Leistner‐Segal
Sandra Leistner‐Segal
MSMaria Teresa Vieira Sanseverino
Maria Teresa Vieira Sanseverino

18 February 2014 in PLOS ONE
Verified
Journal Article
Open access
PDF file
ASAndré Anjos da Silva
André Anjos da Silva
TRTani Maria Schilling Ranieri
Tani Maria Schilling Ranieri
FTFernanda Duarte Torres
Fernanda Duarte Torres
FVFernanda SL Vianna
Fernanda SL Vianna
GPGraziella Rangel Paniz
Graziella Rangel Paniz
MSMaria Teresa Vieira Sanseverino
Maria Teresa Vieira Sanseverino
The emergence of a new subtype of the influenza virus in 2009 generated interest in the international medical community, the media, and the general population. Pregnant women are considered to be a group at risk of serious complications related to the H1N1 influenza virus. The aim of this study was to evaluate the outcomes and teratogenic effects of pregnancies exposed to the H1N1 virus during the Influenza A epidemic that occurred in the state of Rio Grande do Sul in 2009. This is an uncontrolled prospective cohort study of pregnant women with suspected symptoms of Influenza A who were reported in the Information System for Notifiable Diseases – Influenza (SINAN-Influenza) during the epidemic of 2009 (database from the state of Rio Grande do Sul, Brazil). There were 589 cases of pregnant women with suspected infection. Among these, 243 were tested by PCR and included in the analysis. The main outcome measures were: maternal deaths, pregnancy outcome, stillbirths, premature births, low birth weight, congenital malformations, and odds ratios for H1N1+ and non-H1N1 pregnant women. There were one hundred and sixty-three (67%) confirmed cases of H1N1, 34 cases (14%) of seasonal Influenza A and 46 (19%) who were negative for Influenza A. There was no difference between the three groups in clinical parameters of the disease. There were 24 maternal deaths — 18 of them had H1N1. There were 8 stillbirths — 5 were children of H1N1 infected mothers. There were no differences in perinatal outcomes. The present data do not indicate an increase in teratogenic risk from exposure to the influenza A (H1N1) virus. These results will help to strengthen the data and clarify the health issues that arose after the pandemic.

1 January 2002 in Ciencia & Saude Coletiva
Verified
Journal Article
Open access
PDF file
LSLavinia Schuler-Faccini
Lavinia Schuler-Faccini
JLJúlio César Loguercio Leite
Júlio César Loguercio Leite
MSMaria Teresa Vieira Sanseverino
Maria Teresa Vieira Sanseverino
RPRossana Mizunski Peres
Rossana Mizunski Peres
O fato de agentes ambientais, nomeadamente fármacos, infecções maternas, e agentes químicos ou físicos poderem causar danos ao embrião ou feto em desenvolvimento é um problema reconhecido principalmente a partir do século 20. Nos países em desenvolvimento, existem características especiais que podem tornar esse problema mais agudo. Essas características incluem níveis educacionais e econômicos baixos da população, alta incidência de doenças infecciosas e carenciais, escassos recursos para saúde e pesquisa, prática freqüente e sem controle de automedicação, facilidade de obtenção de medicações que deveriam estar submetidas à prescrição médica e, finalmente, proibição legal de interrupção da gestação. Além disso, pode somar-se uma qualidade ambiental precária ou mesmo condições de trabalho insalubres durante a gravidez. No presente trabalho apresentamos as principais metodologias para detecção e monitorização de potenciais teratógenos, com ênfase especial nos programas desenvolvidos no Brasil e América Latina.