Montagnana Martina, Danese Elisa, Giontella Alice, Bonafini Sara, Benati Marco, Tagetti Angela, Dalbeni Andrea, Cavarzere Paolo, Gaudino Rossella, Pucci Mairi, Salvagno Gian Luca, Antoniazzi Franco, Lippi Giuseppe, Maffeis Claudio, Fava Cristiano
Section of Clinical Biochemistry, Department of Neuroscience, Biomedicine and Movement Science, University of Verona, 37134 Verona, Italy.
"General Medicine and Hypertension" Unit, Department of Medicine, University of Verona, 37134 Verona, Italy.
Diagnostics (Basel). 2020 Nov 20;10(11):977. doi: 10.3390/diagnostics10110977.
Childhood obesity is becoming a major health issue and contributes to increasing the risk of cardiovascular disease in adulthood. Since dysregulated metabolism of bile acids (BAs) plays a role in progression of obesity-related disorders, including steatosis and hypertension, this study aimed to investigate BAs profiles in obese children with and without steatosis and hypertension, as well as exploring the interplay between BAs profile and vascular function.
BAs concentrations were quantified with liquid chromatography-tandem mass spectrometry in 69 overweight/obese children and adolescents (mean age, 11.6 ± 2.5 years; 30 females). Liver steatosis was defined with abdomen ultrasonography, whilst hypertension was defined according to the current European guidelines. Vascular function was assessed with ultrasound technique, by measuring carotid intima media thickness (cIMT) and common carotid artery distensibility (cDC).
Total and individual glycine-conjugated BAs concentrations were found to be significantly higher in males compared to females, as well as in pre-pubertal compared to pubertal stage ( < 0.05 for both). No difference in BAs concentration was observed between hypertensive and normotensive subjects. Total BAs and glycine conjugated BAs were significantly higher in participants with steatosis compared to those without ( = 0.004 for both). The values of total glycine-conjugate acids were positively correlated with cDC and this association remained significant in linear regression after adjusting for sex, age, pubertal stage, body mass index and aspartate aminotransferase.
The results suggest a possible role of BAs in the pathogenesis of liver and/or vascular damage in children and adolescent. Further studies are hence needed to validate these preliminary findings.
儿童肥胖正成为一个主要的健康问题,并导致成年后患心血管疾病的风险增加。由于胆汁酸(BAs)代谢失调在肥胖相关疾病(包括脂肪变性和高血压)的进展中起作用,本研究旨在调查有无脂肪变性和高血压的肥胖儿童的胆汁酸谱,并探讨胆汁酸谱与血管功能之间的相互作用。
采用液相色谱 - 串联质谱法对69名超重/肥胖儿童和青少年(平均年龄11.6±2.5岁;30名女性)的胆汁酸浓度进行定量。通过腹部超声检查定义肝脏脂肪变性,同时根据当前欧洲指南定义高血压。采用超声技术,通过测量颈动脉内膜中层厚度(cIMT)和颈总动脉扩张性(cDC)来评估血管功能。
发现男性的总胆汁酸和个别甘氨酸结合胆汁酸浓度显著高于女性,青春期前儿童的浓度也显著高于青春期儿童(两者均P<0.05)。高血压和血压正常的受试者之间胆汁酸浓度无差异。与无脂肪变性的参与者相比,有脂肪变性的参与者的总胆汁酸和甘氨酸结合胆汁酸显著更高(两者均P = 0.004)。总甘氨酸结合酸的值与cDC呈正相关,在调整性别、年龄、青春期阶段、体重指数和天冬氨酸转氨酶后,这种关联在多元线性回归中仍然显著。
结果表明胆汁酸在儿童和青少年肝脏和/或血管损伤的发病机制中可能起作用。因此,需要进一步研究来验证这些初步发现。