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1.
Int J Obes (Lond) ; 41(6): 976-981, 2017 06.
Artículo en Inglés | MEDLINE | ID: mdl-28293019

RESUMEN

BACKGROUND: Adipokines could pose a link between adiposity, systemic inflammation and metabolic disease risk. However, it is unclear whether representative biomarkers are methodologically suitable for use in human obesity research. METHODS: We assessed the intra-individual reproducibility of selected adipokines in a sample of 207, apparently healthy, participants with available biosample collections over a 4-month period. Concentrations of the following adipokines were measured at each sampling time point: fatty-acid binding protein-4 (FABP-4), lipocalin-2, monocyte chemoattractant protein 1 (MCP-1), procalcitonin, progranulin, vaspin and visfatin/Nampt. We calculated intraclass correlation coefficients (ICC) and examined Bland-Altman plots. RESULTS: The analyses suggested an overall good to excellent biomarker reproducibility over 4 months: FABP-4: ICC=0.73 (95% confidence interval: 0.65, 0.78), lipocalin-2: 0.64 (0.55, 0.71), MCP-1: 0.85 (0.81; 0.89), procalcitonin: 0.78 (0.72, 0.83), progranulin: 0.59 (0.50, 0.68) and vaspin: 0.86 (0.82, 0.89). A good agreement of the repeated measurements was further supported by the Bland-Altman plots. No substantial differences in biomarker performance according to adiposity status could be observed. Reliability of visfatin/Nampt could not be assessed due to a high number of measurements below the lower limit of detection. CONCLUSION: Results suggest that single measurements of the evaluated adipokines could be used in population-based studies aimed to assess links between obesity, inflammation and metabolic diseases.


Asunto(s)
Adipoquinas/metabolismo , Adiposidad/fisiología , Investigación Biomédica/métodos , Citocinas/metabolismo , Inflamación/fisiopatología , Enfermedades Metabólicas/fisiopatología , Nicotinamida Fosforribosiltransferasa/metabolismo , Obesidad/fisiopatología , Adulto , Biomarcadores/metabolismo , Investigación Biomédica/tendencias , Femenino , Alemania , Humanos , Inflamación/etiología , Inflamación/metabolismo , Resistencia a la Insulina , Masculino , Enfermedades Metabólicas/etiología , Persona de Mediana Edad , Obesidad/complicaciones , Obesidad/metabolismo , Valor Predictivo de las Pruebas , Estudios Prospectivos , Reproducibilidad de los Resultados , Circunferencia de la Cintura
2.
Nat Commun ; 13(1): 936, 2022 02 17.
Artículo en Inglés | MEDLINE | ID: mdl-35177612

RESUMEN

Metabolic alterations precede cardiometabolic disease onset. Here we present ceramide- and dihydroceramide-profiling data from a nested case-cohort (type 2 diabetes [T2D, n = 775]; cardiovascular disease [CVD, n = 551]; random subcohort [n = 1137]) in the prospective EPIC-Potsdam study. We apply the novel NetCoupler-algorithm to link a data-driven (dihydro)ceramide network to T2D and CVD risk. Controlling for confounding by other (dihydro)ceramides, ceramides C18:0 and C22:0 and dihydroceramides C20:0 and C22:2 are associated with higher and ceramide C20:0 and dihydroceramide C26:1 with lower T2D risk. Ceramide C16:0 and dihydroceramide C22:2 are associated with higher CVD risk. Genome-wide association studies and Mendelian randomization analyses support a role of ceramide C22:0 in T2D etiology. Our results also suggest that (dh)ceramides partly mediate the putative adverse effect of high red meat consumption and benefits of coffee consumption on T2D risk. Thus, (dihydro)ceramides may play a critical role in linking genetic predisposition and dietary habits to cardiometabolic disease risk.


Asunto(s)
Enfermedades Cardiovasculares/epidemiología , Ceramidas/sangre , Diabetes Mellitus Tipo 2/epidemiología , Adulto , Anciano , Biomarcadores/sangre , Biomarcadores/metabolismo , Enfermedades Cardiovasculares/sangre , Enfermedades Cardiovasculares/metabolismo , Ceramidas/metabolismo , Diabetes Mellitus Tipo 2/sangre , Diabetes Mellitus Tipo 2/metabolismo , Femenino , Humanos , Masculino , Metabolómica , Persona de Mediana Edad , Estudios Prospectivos , Medición de Riesgo/métodos , Medición de Riesgo/estadística & datos numéricos
3.
Obes Rev ; 17(11): 1067-1079, 2016 11.
Artículo en Inglés | MEDLINE | ID: mdl-27405372

RESUMEN

Plant-based dietary interventions have been proposed to reduce obesity induced chronic low-grade inflammation and hence prevent chronic disease risk; however, human evidence remains unclear. This systematic review and meta-analysis of intervention trials aimed to assess the effect of plant-based diets on obesity-related inflammatory biomarker profiles. Medline, EMBASE and Cochrane Central Register of Controlled Trials (CENTRAL) were searched for articles published until January 2016 and mean differences in biomarkers of inflammatory status were assessed for: C-reactive protein (CRP), interleukin-6 (IL-6), tumour necrosis factor-alpha (TNF-ɑ), soluble intercellular adhesion molecule 1 (sICAM), leptin, adiponectin and resistin. Of initially identified 2,583 publications, 29 met the meta-analysis inclusion criteria [a total of 2,689 participants]. Consumption of plant-based diets was associated with a reduction in the mean concentrations of the following biomarkers: CRP [effect size, -0.55 mg/l, 95% confidence intervals (CI): -0.78; -0.32, I2 = 94.4%], IL-6 [effect size, -0.25 ng/l, 95% CI: -0.56; 0.06, I2 = 74%], and, to some degree, sICAM (-25.07 ng/ml [95% CI: -52.32; 2.17, I2 = 93.2%]). No substantial effects were revealed for TNF-ɑ, resistin, adiponectin and leptin. Plant-based diets are associated with an improvement in obesity-related inflammatory profiles and could provide means for therapy and prevention of chronic disease risk.


Asunto(s)
Dieta Saludable , Dieta Vegana , Inflamación/dietoterapia , Inflamación/etiología , Obesidad/complicaciones , Obesidad/dietoterapia , Biomarcadores , Enfermedad Crónica , Ensayos Clínicos Controlados como Asunto , Humanos , Inflamación/inmunología , Inflamación/patología , Interleucina-6 , Obesidad/inmunología , Obesidad/patología
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