Juana Sánchez-Villamil

Juana Sánchez-Villamil


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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1 December 2016 in The International Journal of Biochemistry & Cell Biology
Verified
Journal Article
Closed access
JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
VDVerónica D’annunzio
Verónica D’annunzio
PFPaola V. Finocchietto
Paola V. Finocchietto
SHSilvia Holod
Silvia Holod
IRInés Rebagliati
Inés Rebagliati
MCMaría C. Carreras
María C. Carreras

26 March 2020 in Oxidative Medicine and Cellular Longevity
Verified
Journal Article
Open access
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JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
PBPaula K Bautista-Nino
Paula K Bautista-Nino
NSNorma C. Serrano
Norma C. Serrano
MRMelvin Y. Rincon
Melvin Y. Rincon
NGNisha Garg
Nisha Garg
Chagas disease (CD) is one of the most important neglected tropical diseases in the American continent. Host-derived nitroxidative stress in response to Trypanosoma cruzi infection can induce tissue damage contributing to the progression of Chagas disease. Antioxidant supplementation has been suggested as adjuvant therapy to current treatment. In this article, we synthesize and discuss the current evidence regarding the use of antioxidants as adjunctive compounds to fight harmful reactive oxygen species and lower the tissue oxidative damage during progression of chronic Chagas disease. Several antioxidants evaluated in recent studies have shown potential benefits for the control of oxidative stress in the host’s tissues. Melatonin, resveratrol, the combination of vitamin C/vitamin E (vitC/vitE) or curcumin/benznidazole, and mitochondria-targeted antioxidants seem to be beneficial in reducing plasma and cardiac levels of lipid peroxidation products. Nevertheless, further research is needed to validate beneficial effects of antioxidant therapies in Chagas disease.

1 May 2020 in Biomédica
Verified
Journal Article
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JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
CPCarolina Pino-Vélez
Carolina Pino-Vélez
JTJuanita Trejos-Suárez
Juanita Trejos-Suárez
NCNestor Cardona
Nestor Cardona
AEAna Lucía España
Ana Lucía España
PAPedro A. Alfonso
Pedro A. Alfonso
Introduction: Periodontitis affects more than 20% of the Latin American population.Oxidative markers are associated with greater progression of periodontitis; therefore, its role in pathogenesis should be studied.Objective: To determine the prevalence of the main oral bacteria and viruses associated with periodontitis and estimate the total antioxidant capacity and lipid peroxidation in saliva from patients with periodontitis.Materials and methods: We conducted systemically a cross-sectional study in 101 healthy subjects, 87 of whom had been diagnosed with periodontitis (P), according to the criteria of the Centers of Disease Control and Prevention and the American Academy of Periodontology, and 14 without periodontal pockets as controls (C). In subgingival samples, major viruses and dental pathogenic bacteria were identified using PCR techniques. The levels of total antioxidant capacity and malon-di-aldehyde (MDA) were determined by spectrophotometry in samples of unstimulated saliva.Results: The mean of periodontal depth pocket and clinical attachment loss in patients with periodontitis was 5.6 ± 1.7 and 6.1 ± 3.1 mm, respectively. The most prevalent microorganisms were Aggregatibacter actinomycetemcomitans (32.5%) and Porphyromonas gingivalis (18.6%). The patients from rural areas showed a higher percentage of A. actinomycetemcomitans (urban: 17.9% vs. rural: 48.9%, p=0.0018). In patients with periodontitis, the frequency of EBV, HSV1 & 2, and HCMV genes was 2.3%. Periodontitis patients had higher levels of MDA (P: 2.1 ± 1.5; C: 0.46 ± 0.3 μmol/g protein; p=0.0001) and total antioxidant capacity (P: 0.32 ± 0.2; C: 0.15 ± 0.1 mM; p< 0.0036). Oxidative markers showed no modifications due to the presence of periodontopathic bacteria.Conclusions: Aggregatibacter actinomycetemcomitans was the most prevalent bacteria; its presence did not modify the levels of oxidative markers in the saliva of patients with periodontitis.

9 November 2015 in Biomédica
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Journal Article
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JBJefferson Antonio Buendia
Jefferson Antonio Buendia
JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
GUGabriela Urman
Gabriela Urman
Introducción. La infección bacteriana severa en menores de 2 años con fiebre sin foco, a pesar de los avances en vacunación, sigue siendo un motivo de preocupación para médicos y padres. Contar con información de costo-efectividad es relevante para la toma de decisiones en este escenario clínico.Objetivo. Evaluar la costo-efectividad de 4 estrategias para la detección de infección bacteriana severa en lactantes febriles sin foco en la Argentina.Materiales y métodos. Mediante la técnica de árbol de decisiones, en una cohorte hipotética de 10.000 pacientes, se evaluó la costo-efectividad de cuatro estrategias para la detección de infección bacteriana severa: Escala de Rochester + Proteína C reactiva, Escala de Rochester + Procalcitonina , Escala de Rochester y conducta expectante.Resultados. La estrategia Escala de Rochester + Proteína C reactiva resultó ser la más costo-efectiva al obtener una razón de costo efectividad incremental de US$ 784 por caso correctamente diagnosticado frente a los US$ 839 de Escala de Rochester + Procalcitonina, US$ 1,116 en conducta expectante o US$1193 de la Escala de Rochester. En el análisis de sensibilidad se determinó que, ante probabilidades de infección bacteriana severa, iguales o menores del 14% la estrategia de elección es la conducta expectante.Conclusiones. La utilización combinada de la Escala de Rochester + Proteína C constituyo la estrategia más costo efectiva para la detección de infección bacteriana severa en lactantes febriles sin foco de 1 a 3 meses. Sin embargo, en escenarios de bajo riesgo de infección bacteriana severa el manejoexpectante constituye la estrategia de elección.

18 September 2019 in BMC Research Notes
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Journal Article
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JBJefferson Antonio Buendia
Jefferson Antonio Buendia
JCJosé Armando Justinico Castro
José Armando Justinico Castro
LVLaura Joanna Tapia Vela
Laura Joanna Tapia Vela
DSDenis Sinisterra
Denis Sinisterra
JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
Andres F. ZuluagaAndres F. Zuluaga
Andres F. Zuluaga
Objective: The aim of this study was to compare in vivo effect of five pharmacological options on inflammation and pulmonary fibrosis induced by paraquat. Methods: 54 Wistar SPF rats were used. After 2 h post-intoxication with paraquat ion, groups of 9 animals were randomly assigned to (1) cyclophosphamide plus dexamethasone (2) low molecular weight heparin (3) unfractionated heparin (4) vitamin C every 24 h, (5) atorvastatin or (6) placebo with intraperitoneal saline. Lung inflammation, alveolar injury, hepatocyte damage, hepatic regeneration, acute tubular necrosis and kidney congestion were evaluated. Results: In the control group 100% of animals presented moderate and severe lung inflammation, while in the groups with atorvastatin and intratracheal heparin this proportion was lower (55.5%; CI 26.6–81.3%) (p = 0.025). A lower degree of moderate or severe hepatic regeneration was evident in the treatment groups with atorvastatin (p = 0.009). In this study was demonstrated that statins and heparin might have a protective effect in the paraquat-induced destructive phase. More evidence is needed to evaluated of dose–response effects of these drugs before to study in clinical trials.

1 October 2008 in Revista de Salud Pública
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Journal Article
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JBJefferson Antonio Buendia
Jefferson Antonio Buendia
JLJosé J. Lopez-Gutierrez
José J. Lopez-Gutierrez
OGOscar A. Garcia-Vega
Oscar A. Garcia-Vega
JDJorge Diaz-Rojas
Jorge Diaz-Rojas
JSJuana Sánchez-Villamil
Juana Sánchez-Villamil
Determining prescription patterns for outpatient medication authorised for patients affiliated to an EPS and assisted by medium- and high-level complexity IPS. This was a cross-sectional study where medication prescription was evaluated in 331 second- and third-level complexity hospitals from 27 Colombian departments during 2006. 38 863 prescriptions for 3 663 patients' medication were analysed. 61,4 % came from third-level complexity hospitals, mainly for patients affiliated to contribution-based regimes. Average prescribed medication per person was 2,2 (2,1-2,2 95 % CI), the percentage of antibiotics formulated by prescription was 29,2 % (28,7-29,6 95 % CI), essential prescribed medicines accounted for 64,2 % (63,7-64,6 95 % CI) and injectable medicines was 22,1 % (21,7-25,5 %). More than half the medications (62,1 %; 61,5-62,7 95 % CI) were in ATC groups such as anti-infectious agents, immunomodulating agents and medications for the alimentary and metabolic tract. DU90% consisted of 64 medications, medication consumption being 8,39 daily de-fined doses (DDD)/1 000 patients, costing 5 216 Colombian pesos per DDD. This analysis led to identifying medications whose formulation frequency did not correlate with an epidemiologic profile as immunomudulator and growth-hormone (somatotropin) agents. There were differences in the frequency and quantity of DDD medications authorised by type of affiliation which could thus be providing evidence of obstacles to the population having access to drugs/medicaments.