Helena Medina Cruz

Dr. Helena Medina Cruz


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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7 July 2011 in Journal of Medical Virology
Verified
Journal Article
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LVLivia Melo Villar
Livia Melo Villar
JOJaqueline Correia de Oliveira
Jaqueline Correia de Oliveira
HCHelena Medina Cruz
Helena Medina Cruz
CYClara Fumiko Tachibana Yoshida
Clara Fumiko Tachibana Yoshida
ELElisabeth Lampe
Elisabeth Lampe
LLLia Laura Lewis‐Ximenez
Lia Laura Lewis‐Ximenez

1 January 2015 in World Journal of Virology
Verified
Journal Article
Open access
LVLivia Melo Villar
Livia Melo Villar
HCHelena Medina Cruz
Helena Medina Cruz
JBJakeline Barbosa
Jakeline Barbosa
CBCristianne Bezerra
Cristianne Bezerra
MPMoyra Machado Portilho
Moyra Machado Portilho
LSLetícia de Paula Scalioni
Letícia de Paula Scalioni
Update on hepatitis B and C virus diagnosis

1 July 2014 in Journal of Clinical Virology
Verified
Journal Article
Closed access
LSLeticia de Paula Scalioni
Leticia de Paula Scalioni
HCHelena Medina Cruz
Helena Medina Cruz
VPVanessa de Paula
Vanessa de Paula
JMJuliana Custódio Miguel
Juliana Custódio Miguel
VMVanessa Alves Marques
Vanessa Alves Marques
LVLivia Melo Villar
Livia Melo Villar

1 January 2011 in Journal of Clinical Laboratory Analysis
Verified
Journal Article
Open access
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HCHelena Medina Cruz
Helena Medina Cruz
ESElisangela Ferreira da Silva
Elisangela Ferreira da Silva
CVCristiane Villela-Nogueira
Cristiane Villela-Nogueira
LNLetícia C. Nabuco
Letícia C. Nabuco
KÓKycia Maria Rodrigues Do Ó
Kycia Maria Rodrigues Do Ó
LVLivia Melo Villar
Livia Melo Villar
In this study, a modified enzyme immunoassay (EIA) was evaluated for the Hepatitis B surface antigen (HBsAg) among whole saliva and oral fluid samples. Specimens were collected from 115 individuals who gave serum and oral fluid using Salivette (Sarstedt, Nümbrecht, Germany) and whole saliva. Saliva specimens were tested following a modified ELISA, and the results were compared with paired serum specimens that were tested according to the supplier's instructions. Transport buffer for the oral fluids, sample volume for assay, incubation period of sample with conjugate as well as cut‐off values were evaluated to optimize the assay. The highest sensitivity and specificity were obtained by increasing the incubation of sample and conjugate to 16 hr and using the area under the receiver operating characteristic curve to calculate cut‐off values. HBsAg was detected in 40 oral fluids and 44 whole saliva samples out of 47 paired positive serum specimens and not detected in 64 oral fluids and 63 whole saliva samples out of 68 matched negative sera samples by the ELISA assay. There was excellent agreement between the results for the serum and saliva specimens kappa value (κ): 0.80 for oral fluid and κ: 0.87 for whole saliva and there was excellent reproducibility. Using an optimized protocol, the sensitivities of whole saliva and oral fluid were 93.6 and 85.1%, respectively, whereas specificities of whole saliva and oral fluid were 92.6 and 94.1%, respectively. Our data showed a significant promise for the use of whole saliva and oral fluid together with the modified commercial EIA for Hepatitis B virus infection surveillance. J. Clin. Lab. Anal. 25:134–141, 2011.

1 April 2019 in Canadian Journal of Gastroenterology and Hepatology
Verified
Journal Article
Open access
LVLivia Melo Villar
Livia Melo Villar
CBCristianne Bezerra
Cristianne Bezerra
HCHelena Medina Cruz
Helena Medina Cruz
MPMoyra Machado Portilho
Moyra Machado Portilho
GFGeane Lopes Flores
Geane Lopes Flores
Hepatitis B virus (HBV) is one of the major causes of chronic liver disease worldwide; however most of individuals are not aware about the infection. Oral fluid and dried blood spot (DBS) samples may be an alternative to serum to HBV diagnosis to increase the access to diagnosis in remote areas or high-risk groups. The main objective of this review is to give an insight about the usefulness of oral fluid and DBS for detecting HBV markers. Several groups have evaluated the detection of HBsAg, anti-HBc, and anti-HBs markers in oral fluid and DBS samples demonstrating 13 to 100% of sensitivity and specificity according different groups, sample collectors, and diagnosis assays. In the same way, HBV DNA detection using oral fluid and DBS samples demonstrate different values of sensitivity according type of collection, studied group, extraction, and detection methods. Thus, serological and molecular diagnostic tests demonstrated good performance for detecting HBV using oral fluid and DBS according some characteristics and could be useful to increase the access to the diagnosis of HBV.

20 August 2018 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
LVLivia Melo Villar
Livia Melo Villar
FMFlavio Augusto Pádua Milagres
Flavio Augusto Pádua Milagres
ELElisabeth Lampe
Elisabeth Lampe
HCHelena Medina Cruz
Helena Medina Cruz
LSLeticia de Paula Scalioni
Leticia de Paula Scalioni
VPVanessa de Paula
Vanessa de Paula
This study was conducted to determine the prevalence of HBV, HCV, and HDV in urban populations and Amerindians living in the state of Tocantins (Eastern Amazon). A total of 948 individuals were recruited in Tocantinopolis city (Tocantins state) of whom 603 were Amerindians (from 6 tribes) and 345 were non-Amerindians (6 urban areas of Tocantinópolis city). Anti-HCV, HBsAg, anti-HBc, anti-HBs, anti-HBc IgM, anti-HBe, HBeAg, and anti-delta antibodies were determined using enzyme immunoassay. HBV cleared infection (both anti-HBc/anti-HBs+), chronic inactive/immune controlled HBV infection (anti-HBc + only), previous HBV vaccination (anti-HBs + only), active HBV infection (HBsAg+), individuals susceptible to HBV, and anti-HCV reactivity were found in 12.9, 1.8, 27.2, 0.5, 57.7, 1.2% in Amerindians and 12.1, 2.0, 37.1, 0.3, 55.4, 0.3% in non-Amerindians respectively. Out of 139 anti-HBc reactive individuals, 70 were anti-HBe reactive and none presented HBeAg or anti-HBc IgM. Anti-HBc prevalence was associated to older age (p < 0.0001). Overall anti-Delta prevalence was 0.3% and regarding anti-HBc reactive individuals, anti-delta prevalence was 3.4 and 0% in Amerindians and non-Amerindians respectively. Overall low prevalence of HBV and HCV infection was found in the populations studied, but high HBV and HCV prevalence was observed in Amerindians compared to non-Amerindians suggesting that these individuals have a higher likelihood of acquiring to these infections. Anti-delta antibodies were found among Amerindians from Eastern Amazon suggesting a risk for this population. Of note is that nearly half of Amerindians had no anti-HBs, indicating a need for HBV vaccination campaigns in this population.