Postprandial Hypertriglyceridemia Is Associated with the Variant 54 Threonine FABP2 Gene.

Purpose: Fasting or postprandial hypertriglyceridemia is considered an independent cardiovascular disease (CVD) risk factor. The intestinal fatty acid binding protein (FABP2) is involved in the intracellular transport and metabolism of fatty acids. The presence of the Ala54Thr polymorphism of the FABP2 gene appears to be involved in postprandial hypertriglyceridemia. We explored the possible association of the Ala54Thr polymorphism with fat intolerance in apparently healthy, fasting, normolipidemic subjects with normal body-mass index and without diabetes. Methodology: A total of 158 apparently healthy individuals were classified as fat tolerant (n = 123) or intolerant (n = 35) according to their response (plasma triglycerides) to an oral abbreviated tolerance test with blood samples taken at 0, 2 and 4 h. At 0 h, all subjects ingested 26.3 g of fats. Presence of the Ala54Thr polymorphism of the FABP2 gene was evaluated by polymerase chain reaction⁻restriction fragment length (PCR⁻RFLP). Results: The group with fat intolerance (postprandial hypertriglyceridemia group) showed an increased frequency of the Thr54Thr genotype when compared with the group with normal fat tolerance (control group) (23% vs. 4%, respectively, OR: 16.53, 95% CI: 4.09⁻66.82, p: 0.0001, pc: 0.0003). Carriers of at least one Thr54 allele were up to six times more prevalent in the fat intolerant group than in the non-carriers. (OR: 6.35; 95% CI: 1.86⁻21.59, p: 0.0003, pc: 0.0009). The levels of plasma triglycerides (Tg) at 4 h after the test meal were higher in carriers of at least one 54Thr allele than in carriers of the Ala54 allele (p < 0.05). Conclusions: There is a significant association between postprandial hypertriglyceridemia and the presence of at least one 54Thr allele of the FABP2 gene. In addition, subjects with this genotype showed an increased ratio of Tg/HDL-cholesterol. This parameter is a marker of increased CVD risk and insulin resistance.

Estudio observacional de la microbiota intestinal aeróbica / Observational study of the aerobic gut microbiota

El ecosistema microbiano asociado al intestino es el más diverso y complejo, en el ser humano cambia durante las diferentes etapas de la vida. La pérdida del equilibrio de este ecosistema intestinal se conoce como disbiosis. Establecer la posible relación entre la disbiosis aeróbica con diversas enfermedades de interés clínico encontradas. Se estudiaron 377 casos de disbiosis con diferentes patologías como trastorno del espectro autista (TEA), enfermedad inflamatoria intestinal, alergias, intolerancia alimentaria, entre otras; y un grupo control de 497 personas aparentemente sanas. Para el análisis de la información se utilizaron las pruebas de T de Student y regresión logística multinominal, ajustadas a un intervalo de confianza del 95%. Hubo variabilidad en el crecimiento de la microbiota benéfica del grupo de casos de disbiosis respecto al grupo control (p<0,001). La microbiota transitoria causante de disbiosis estuvo conformada principalmente por cocos grampositivos: Streptococcus grupo viridans, Enterococcus faecium y Enterococcus gallinarum; bacilos gramnegativos: Klebsiella pneumoniae, complejo Enterobacter cloacae y Klebsiella oxytoca y especies de Candida albicans, Candida tropicalis y complejo Candida parapsilosis. La población más susceptible con disbiosis fueron niños con edades comprendidas entre 2 y 6 años. Los TEA y la intolerancia alimentaria estuvieron asociados significativamente con la disbiosis (p<0,05)

The microbial ecosystem associated with the intestine is the most diverse and complex in the human being, since it changes during the different stages of life. Losing balance of this intestinal ecosystem is known as dysbiosis. To establish the possible relationship between aerobic dysbiosis and diseases of clinical interest found. Three hundred and seventy-seven (377) cases of dysbiosis with different pathologies such as autism spectrum disorder (ASD), inflammatory bowel disease, allergies, food intolerance, among others; and a control group of 497 apparently healthy people, were studied. For the analysis of the information, multinomial logistic regression and Student's t tests were used, adjusted to a 95% confidence interval. The growth of beneficial microbiota showed variability in the dysbiosis case group compared to the control group (p <0.001). The transient microbiota causing dysbiosis was mainly made up of gram-positive cocci: Streptococcus viridans group, Enterococcus faecium and Enterococcus gallinarum; gram-negative bacilli: Klebsiella pneumoniae, Enterobacter cloacae complex, and Klebsiella oxytoca and Candida albicans, Candida tropicalis and Candida parapsilosis complex species. The most susceptible population with dysbiosis was children aged between 2 and 6 years. The ASD and food intolerance were significantly associated with dysbiosis (p <0.05)