Browsing by Author "Santos, José L."

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    Adaptación y análisis factorial del cuestionario de conducta de alimentación del adulto (AEBQ) en idioma español
    (2020) Morales, Eva María; Maghioros, María Ángeles; Obregón, Ana M.; Santos, José L.
    El Cuestionario de Conducta de Alimentación de Adultos (AEBQ, por su sigla en inglés derivada de Adult Eating Behavior Questionnaire) es una de las herramientas psicométricas más usadas para evaluar la conducta de alimentación. El objetivo de este estudio fue adaptar y analizar factorialmente la versión en idioma español del AEBQ. El cuestionario adaptado al idioma español se aplicó en un estudio piloto de 50 voluntarias universitarias entre 20 y 30 años de edad. Se utilizó la técnica de análisis factorial para reducir la dimensionalidad de los datos y evaluar preliminarmente su estructura. Se usó la estadística alfa de Cronbach para explorar la consistencia interna del cuestionario adaptado. El análisis factorial reveló una estructura de 8 factores que explican el 82,8 % de la variación de los datos, lo que es concordante con el número de dimensiones de la conducta de alimentación publicada para el AEBQ original. La consistencia interna fue alta, con valores de la estadística α de Cronbach entre 0,77 y 0,91 para las 8 dimensiones consideradas. En conclusión, la versión adaptada al idioma español del AEBQ presenta una razonable concordancia en su estructura de datos con el cuestionario publicado originalmente en inglés, así como una adecuada consistencia interna. Se deben realizar futuros estudios de mayor tamaño muestral que incluyan participantes de diferentes grupos de edad, sexo y estado nutricional.
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    Differential methylation pattern in pubertal girls associated with biochemical premature adrenarche
    (2023) Ponce, Diana; Rodríguez, Fernando; Miranda, José P.; Binder, Alexandra M.; Santos, José L.; Michels, Karin B.; Cutler, Gordon B.; Pereira, Ana; Iñiguez, Germán; Mericq, Verónica
    Biochemical premature adrenarche is defined by elevated serum DHEAS [≥40 μg/dL] before age 8 y in girls. This condition is receiving more attention due to its association with obesity, hyper-insulinemia, dyslipidemia, and polycystic ovary syndrome. Nevertheless, the link between early androgen excess and these risk factors remains unknown. Epigenetic modifications, and specifi-cally DNA methylation, have been associated with the initiation and progression of numerous disorders, including obesity and insulin resistance. The aim of this study was to determine if prepubertal androgen exposure is associated with a different methylation profile in pubertal girls. Eighty-six healthy girls were studied. At age 7 y, anthropometric measurements were begun and DHEAS levels were determined. Girls were classified into Low DHEAS (LD) [<42 μg/dL] and High DHEAS (HD) [≥42 μg/dL] groups. At Tanner stages 2 and 4 a DNA methylation microarray was performed to identify differentially methylated CpG positions (DMPs) between HD and LD groups. We observed a differential methylation pattern between pubertal girls with and without bio-chemical PA. Moreover, a set of DNA methylation markers, selected by the LASSO method, successfully distinguished between HD and LD girls regardless of Tanner stage. Additionally, a subset of these markers were significantly associated with glucose-related measures such as insulin level, HOMA-IR, and glycaemia. This pilot study provides evidence consistent with the hypothesis that high DHEAS concentration, or its hormonally active metabolites, may induce a unique blood methylation signature in pubertal girls, and that this methylation pattern is associated with altered glucose metabolism.
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    DNA methylation in genes of longevity-regulating pathways: association with obesity and metabolic complications
    (2019) Salas Pérez, Francisca; Ramos López, Omar; Mansego, María L.; Milagro, Fermín I.; Santos, José L.; Riezu-Boj, José I.; Alfredo Martínez, J.
    Aging is the main risk factor for most chronic diseases. Epigenetic mechanisms, such as DNA methylation (DNAm) plays a pivotal role in the regulation of physiological responses that can vary along lifespan. The aim of this research was to analyze the association between leukocyte DNAm in genes involved in longevity and the occurrence of obesity and related metabolic alterations in an adult population. Subjects from the MENA cohort (n=474) were categorized according to age (<45 vs 45>) and the presence of metabolic alterations: increased waist circumference, hypercholesterolemia, insulin resistance, and metabolic syndrome. The methylation levels of 58 CpG sites located at genes involved in longevity-regulating pathways were strongly correlated (FDR-adjusted< 0.0001) with BMI. Fifteen of them were differentially methylated (p<0.05) between younger and older subjects that exhibited at least one metabolic alteration. Six of these CpG sites, located at MTOR (cg08862778), ULK1 (cg07199894), ADCY6 (cg11658986), IGF1R (cg01284192), CREB5 (cg11301281), and RELA (cg08128650), were common to the metabolic traits, and CREB5, RELA, and ULK1 were statistically associated with age. In summary, leukocyte DNAm levels of several CpG sites located at genes involved in longevity-regulating pathways were associated with obesity and metabolic syndrome traits, suggesting a role of DNAm in aging-related metabolic alterations.
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    Fructose, Omega 3 Fatty Acids, and Vitamin E: Involvement in Pediatric Non-Alcoholic Fatty Liver Disease
    (2020) Alberti, Gigliola; Gana, Juan Cristóbal; Santos, José L.
    Non-alcoholic fatty liver disease (NAFLD) is currently the most common form of liver disease in both adults and children, becoming the leading cause for liver transplant in many countries. Its prevalence has increased considerably in recent years, mainly due to the explosive increase in pediatric obesity rates. NAFLD is strongly associated with central obesity, diabetes, dyslipidemia and insulin resistance, and it has been considered as the hepatic manifestation of the metabolic syndrome. Its complex pathophysiology involves a series of metabolic, inflammatory and oxidative stress processes, among others. Given the sharp increase in the prevalence of NAFLD and the lack of an appropriate pharmacological approach, it is crucial to consider the prevention/management of the disease based on lifestyle modifications such as the adoption of a healthy nutrition pattern. Herein, we review the literature and discuss the role of three key nutrients involved in pediatric NAFLD: fructose and its participation in metabolism, Omega-3 fatty acids and its anti-inflammatory effects and vitamin E and its action on oxidative stress.