andrea canals

Prof. andrea canals

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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15 August 2020 in Revista Panamericana de Salud Pública
Verified
Journal Article
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MCMauricio Canals
Mauricio Canals
CCCristóbal Cuadrado
Cristóbal Cuadrado
andrea canalsandrea canals
andrea canals
KYKarla Yohannessen
Karla Yohannessen
LLLuis A. Lefio
Luis A. Lefio
OAOscar Arteaga
Oscar Arteaga
Objectives.To report the surveillance of COVID-19 pandemic in Chile and analyse the response to public health interventions implemented from 3 March to 30 June 2020 and to assess the risks of collapse of the health care system. Methods.We analysed the effective reproductive number, underreporting of cases, burden of critical beds, case fatality ratio and number of diagnostic RT-PCR for SARS-CoV-2. Results.After an accelerated onset, the COVID-19 pandemic seemed to be relatively controlled in Chile (late April 2020), with reproductive numbers close to 1.00. However, at this time, the load of infected patients was high, with an important number of underreported cases; the diagnostic effort was still limited and heterogeneous across regions. After 1 May up to 30 June a marked exponential increase in the number of cases was observed with a peak on June 14. In this last period the occupation of intensive care unit beds increased to saturation level (89% nationally; 95% in the Metropolitan Region). Conclusions.Our findings suggest that the implemented public health interventions have been initially effective in decreasing the spread of the pandemic. Premature decisions to relax these interventions may have resulted in a rebound in cases with a rapid saturation of the health care system.

1 January 2020 in HPB
Verified
Journal Article
Closed access
FRFrancisco Riquelme
Francisco Riquelme
BMBoris Marinkovic
Boris Marinkovic
MSMarco Salazar
Marco Salazar
WMWaldo Martínez
Waldo Martínez
FCFelipe Catan
Felipe Catan
MUMario Uribe
Mario Uribe

31 March 2021 in Frontiers in Immunology
Verified
Journal Article
Open access
KTKaren Toledo-Stuardo
Karen Toledo-Stuardo
CRCarolina H. Ribeiro
Carolina H. Ribeiro
andrea canalsandrea canals
andrea canals
MMMarcela Morales
Marcela Morales
VGValentina Gárate
Valentina Gárate
MMMaría Carmen Molina
María Carmen Molina
Gastric cancer (GC) is the fifth most prevalent type of cancer worldwide. Gastric tumor cells express MICA protein, a ligand to NKG2D receptor that triggers natural killer (NK) cells effector functions for early tumor elimination.MICAgene is highly polymorphic, thus originating alleles that encode protein variants with a controversial role in cancer. The main goal of this work was to studyMICAgene polymorphisms and their relationship with the susceptibility and prognosis of GC. Fifty patients with GC and 50 healthy volunteers were included in this study. MICA alleles were identified using Sanger sequencing methods. The analysis ofMICAgene sequence revealed 13 MICA sequences and 5 MICA-short tandem repeats (STR) alleles in the studied cohorts We identified MICA*002 (*A9) as the most frequent allele in both, patients and controls, followed by MICA*008 allele (*A5.1). MICA*009/049 allele was significantly associated with increased risk of GC (OR: 5.11 [95% CI: 1.39–18.74],p= 0.014). The analysis of MICA-STR alleles revealed a higher frequency of MICA*A5 in healthy individuals than GC patients (OR = 0.34 [95% CI: 0.12–0.98],p= 0.046). Survival analysis after gastrectomy showed that patients with MICA*002/002 or MICA*002/004 alleles had significantly higher survival rates than those patients bearing MICA*002/008 (p= 0.014) or MICA*002/009 (MICA*002/049) alleles (p= 0.040). The presence of threonine in the position MICA-181 (MICA*009/049 allele) was more frequent in GC patients than controls (p= 0.023). Molecular analysis of MICA-181 showed that the presence of threonine provides greater mobility to the protein than arginine in the same position (MICA*004), which could explain, at least in part, some immune evasion mechanisms developed by the tumor. In conclusion, our findings suggest that the study of MICA alleles is crucial to search for new therapeutic approaches and may be useful for the evaluation of risk and prognosis of GC and personalized therapy.

7 November 2019 in BMJ Open
Verified
Journal Article
Open access
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PCPatricia Caro
Patricia Caro
XGXimena Guerra
Ximena Guerra
andrea canalsandrea canals
andrea canals
Gerardo WeisstaubGerardo Weisstaub
Gerardo Weisstaub
CSCarlos Sandaña
Carlos Sandaña
Objectives Neck circumference has emerged as a predictor of obesity and metabolic syndrome, but its clinical usefulness for different groups of population is not clearly defined. The aim is to evaluate the predictive capacity of neck circumference in order to detect cardiovascular risks (CVRs) on the Chilean population and to compare it with waist circumference performance. Design Cross-sectional study. Setting General Chilean population. Participants Data of 4607 adults aged 18 and over from the Chilean National Health Survey 2009–2010 were analysed. Primary and secondary outcome measures Anthropometrics measures included neck and waist circumference, height and weight. CVR was identified according to the Framingham tables adapted for the Chilean population. Receiver operating characteristics curves and logistic regression models were made to evaluate the performance of neck circumference to predict a moderate/high CVR, comparing it to waist circumference. Results Almost 10% of the sample had a moderate or high CVR. The probability of having a moderate/high cardiovascular risk increase with cervical obesity (OR 1.95, 95% CI 1.04 to 3.68) and central obesity (OR 4.5, 95% CI 2.47 to 8.22). The area under the curves were high for cervical obesity (AUC 81.4%, 95% CI 78.8% to 84.0%) and central obesity (AUC 82.2%, 95% CI 79.7% to 84.7%) and not statistically different (p=0.152). Conclusions Neck obesity has a high capacity to predict moderate/high CVR in the Chilean population. Its good performance appears as an opportunity to use it in clinical practice when waist circumference measurement is difficult to measure and eventually replace the waist circumference measurement as the technique is easier.

1 December 2014 in Revista chilena de infectología
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Journal Article
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MVM Teresa Valenzuela
M Teresa Valenzuela
MSMabel Seoane
Mabel Seoane
andrea canalsandrea canals
andrea canals
PPPaola Pidal
Paola Pidal
JHJuan C Hormazábal
Juan C Hormazábal
JDJanepsy Díaz
Janepsy Díaz
10-valent pneumococcal vaccine (PCV-10) was introduced in 2011 to the National Immunization Program in Chile. It was administered in 4 doses, but in 2012 it was modified to a 3 dose program. This article shows the results of the Laboratory Surveillance System for Streptococcus pneumoniae isolated of invasive disease from 2007 to 2012 and compares the incidence of invasive pneumococcal disease (IPD) by age groups in the prevaccinal (2007-2010) and postvaccinal period (2012). Descriptive study of S. pneumoniae surveillance in invasive diseases cases confirmed at the National Reference Laboratory of the Institute of Public Health of Chile from 2007 to 2012. Global incidence of laboratory confirmed IPD cases decreased 27.8% from 2007 to 2012 and showed a lower risk for IPD in 2012 compared with 2007. Incidence in children aged 1 year or less decreased from 56.1 to 16.3 per 100,000 and from 42.0 to 19.9 per 100,000 in children aged 12 to 23 months in the same period. Highest decreases were observed in IPD cases caused by serotypes 4 (100%), 19F (93.3%), 23F (90.9%), 14 (81.1%), 6B (70%), 18C (58.3%) and 1(81.8%) in children aged 2 years or less. Surveillance System detects S.pneumoniae isolated from invasive diseases, contributing with information about laboratory confirmed IPD trends, prevalent serotypes and replacement effects. These results can be used as evidence in healthcare decision making for pneumococcal vaccines.

24 July 2015 in Medical and Veterinary Entomology
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CGChristian R. González
Christian R. González
CRC. Reyes
C. Reyes
andrea canalsandrea canals
andrea canals
APA. Parra
A. Parra
XMX. Muñoz
X. Muñoz
KRK. Rodríguez
K. Rodríguez