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1.
Med Microbiol Immunol ; 209(6): 693-703, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-32995957

RESUMEN

Microbial translocation (MT) and altered gut microbiota have been described in acute leukemic patients and contribute to immune activation and inflammation. However, phage translocation has not been investigated in leukemia patients yet. We recruited 44 leukemic patients and 52 healthy adults and quantified the levels of 3 phages in peripheral blood, which were the most positive phages screened from fecal samples. The content of 16S rRNA in plasma was detected by qPCR to assess the intestinal mucosa of these patients. Spearman's rank correlation was used to analyze the relationship between phage load and the relevant clinical data. We found the most prevalent phages in fecal samples were λ phage, Wphi phage, and P22 phage, and λ phage had the highest detection rate in plasma (68%). Phage content was affected by chemotherapy and course of disease and correlated with the levels of CRP (r = 0.43, p = 0.003), sCD14 (r = 0.37, p = 0.014), and sCD163 (r = 0.44, p = 0.003). Our data indicate that plasma phage load is a promising marker for gut barrier damage and that gut phage translocation correlates with monocyte/macrophage activation and systemic inflammatory response in leukemic patients.


Asunto(s)
Traslocación Bacteriana , Bacteriófagos/aislamiento & purificación , Microbioma Gastrointestinal , Mucosa Intestinal/efectos de los fármacos , Leucemia Mieloide Aguda/sangre , ARN Bacteriano/sangre , ARN Ribosómico 16S/sangre , Viremia/diagnóstico , Adulto , Anciano , Antígenos CD/sangre , Antígenos de Diferenciación Mielomonocítica/sangre , Antineoplásicos/efectos adversos , Antineoplásicos/farmacología , Proteína C-Reactiva/análisis , Femenino , Humanos , Mucosa Intestinal/microbiología , Leucemia Mieloide Aguda/tratamiento farmacológico , Leucemia Mieloide Aguda/microbiología , Leucemia Mieloide Aguda/virología , Receptores de Lipopolisacáridos/sangre , Activación de Macrófagos , Masculino , Persona de Mediana Edad , Permeabilidad , Leucemia-Linfoma Linfoblástico de Células Precursoras/sangre , Leucemia-Linfoma Linfoblástico de Células Precursoras/tratamiento farmacológico , Leucemia-Linfoma Linfoblástico de Células Precursoras/microbiología , Leucemia-Linfoma Linfoblástico de Células Precursoras/virología , Receptores de Superficie Celular/sangre , Viremia/etiología
2.
J Clin Lab Anal ; 34(7): e23285, 2020 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-32267017

RESUMEN

BACKGROUND: The serum alanine aminotransferase (ALT) level is a critical parameter for evaluating liver injury in non-alcoholic fatty liver disease (NAFLD). However, the currently accepted upper limits of normal (ULN) for serum ALT (ULN-ALT) are debated, as they may be excessively high. METHODS: A total of 1638 children aged 6-16 years, comprising 507 children with normal BMI (500 healthy children and 7 children with NAFLD), 199 overweight children, and 932 obese children, were included in the analysis. We re-evaluated the ULN-ALT in 500 healthy Chinese children using the 95th percentiles of serum ALT levels as revised ULN-ALT. Fatty liver was identified by ultrasound examination. RESULTS: Significant positive correlations between serum ALT levels and body mass index (BMI) were detected in overweight boys (r = .399, P < .001), obese boys (r = .398, P < .001), and obese girls (r = .392, P < .001). The prevalence percentages of NAFLD were 93.6%, 75.8%, and 37.9% in obese boys with serum ALT levels of >50, 25-50, and ≤25 U/L and were 81.6%, 67.9%, and 20.6% in obese girls with serum ALT levels of >40, 20-40, and ≤20 U/L, respectively. CONCLUSION: Serum ALT levels significantly correlated with abnormal BMI values in children, suggesting a rigorous BMI threshold is needed to establish the cutoffs for serum ULN-ALT in children. Besides, the revised serum ULN-ALT can uncover mild liver injury in obese children with NAFLD.


Asunto(s)
Alanina Transaminasa/sangre , Enfermedad del Hígado Graso no Alcohólico/sangre , Obesidad/sangre , Adolescente , Índice de Masa Corporal , Niño , Femenino , Humanos , Masculino , Enfermedad del Hígado Graso no Alcohólico/diagnóstico por imagen , Enfermedad del Hígado Graso no Alcohólico/fisiopatología , Sobrepeso/sangre , Valores de Referencia , Ultrasonografía
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