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[Effect of biliary obstruction on lipoprotein(a) concentration].

作者信息

Calmarza Pilar, Bajador Eduardo, Lapresta Carlos, García Castañón Sandra, de Castro Isabel, Civeira Fernando

机构信息

Servicio de Bioquímica Clínica, Hospital Universitario Miguel Servet, Zaragoza, España.

Servicio de Digestivo, Hospital Universitario Miguel Servet, Zaragoza, España.

出版信息

Clin Investig Arterioscler. 2014 Sep-Oct;26(5):218-23. doi: 10.1016/j.arteri.2014.01.003. Epub 2014 Mar 13.

Abstract

OBJECTIVES

This study was appointed to determine the correlation between the concentration of lipoprotein(a) [Lp(a)], apolipoproteins and lipids with biochemical parameters of liver function in a group of patients with reversible cholestasis. We have also determined the concentration of these parameters once solved the biliary obstruction process.

MATERIAL AND METHODS

Eighteen adults over 17 years with extrahepatic cholestasis were included in the study on a prospective basis, and we determined in them biochemical liver function parameters and lipoprotein metabolism parameters, particularly Lp(a) before and after unblocking.

RESULTS

The concentration of Lp(a) prior to desobstruction was inverse and statistically significantly correlated with the concentration of gamma glutamyl transpeptidase (correlation coefficient [r] = -0.757, P = .018). The concentration of Lp(a) (median = 2.66 mg/dL, interquartile range = 5,62) showed a statistically significant increase (median = 9.72 mg/dL, interquartile range = 28.76, P < .001), once the unblocking was performed. Concentrations of total cholesterol and triglycerides had a statistically significant decrease, and HDL cholesterol and apolipoprotein A-1 showed a statistically significant increase once the unblocking was carried out.

CONCLUSIONS

The concentration of Lp(a) is decreased during cholestasis, although there is a significant simultaneous hypercholesterolemia. Cholestasis has a causal role in lowering Lp(a), because the unblocking of bile duct recovers Lp(a) concentration. Our study supports the concept that bile acids exert a controlling effect on the synthesis of Lp(a) and open a mechanism for the treatment of hyper Lp(a).

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