成年唐氏综合征患者体重指数和脂质过氧化的改变

C.J. Chávez , P. Ortega , A. D’Escrivan , L.E. Miranda , J.Y. Leal M , C. Delgado
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引用次数: 0

摘要

简介和目的:21三体或唐氏综合征(DS)是染色体起源性智力低下的最常见原因,其中肥胖是一个公共卫生问题。肥胖是一种与脂质过氧化和抗氧化机制改变相关的促氧化状态。基因剂量的影响与DS的氧化应激有关。本研究的目的是确定成人DS患者的脂质过氧化状态和体重指数(BMI)的变化。患者与方法随机选取50例正常核型(NK)成人(31.0±6.3岁)和29例DS(28.0±8.7岁)进行前瞻性横断面研究。结果:用硫代巴比妥酸衍生物测定血清丙二醛(MDA)水平。测定成人退行性椎体滑移患者的BMI。使用SPSS 15统计程序对数据进行分析,使用95%置信区间(CI), P< 0.05。与成人NK组(0.5±0.4 nmol / ml)相比,DS组的MDA浓度(0.9±0.7 nmol / ml, P< 0.009)较高。成人退行性椎体滑移患者有72.4%的BMI (n = 21)出现异常。肥胖成人退行性变性和超重成人(BMI = 27.5±1.3)MDA浓度升高(1.3±1.0 nmol / ml),肥胖成人退行性变性无显著降低。结论虽然有报道称无退行性变性的严重肥胖成人中抗氧化酶水平降低,但基因剂量的影响可能是肥胖成人伴退行性变性中脂质过氧化降低的一个促进因素,而不是其病理后果的保护因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alteraciones del índice de masa corporal y peroxidación lipídica en individuos adultos con síndrome de Down

Introduction and objective

: Trisomy 21 or Down's syndrome (DS) is the most common cause of mental retardation of chromosomal origin, in which obesity is a public health problem. Obesity is a pro-oxidant state associated with lipid peroxidation and alterations of antioxidant mechanisms. The effect of gene dosage has been linked to oxidative stress in DS. The objective of this study was to determine the status of lipid peroxidation and changes in body mass index (BMI) in adults with DS.

Patients and method

A prospective and cross-sectional study was conducted on 50 adult subjects (31.0 ± 6.3 years) with normal karyotype (NK) and 29 adults with DS (28.0 ± 8.7 years), randomly selected.

Results

: The serum levels of malondialdehyde (MDA) were analysed by thiobarbituric acid derivatives. The BMI was determined in adults with DS. The data were analysed using the SPSS 15 statistical program, using a 95% confidence interval (CI), P<.05.

Adults with DS showed high concentrations of MDA (0.9 ± 0.7 nmol / ml, P<.009) compared to adult NK group (0.5 ± 0.4 nmol / ml). Abnormality was observed in 72.4% of BMI (n = 21) of adults with DS. Elevated concentrations of MDA (1.3 ± 1.0 nmol / ml) were seen in adults with DS and overweight (BMI = 27.5 ± 1.3), showing no significant decrease in obese adults with DS.

Conclusion

Although a reduction of antioxidant enzymes in severely obese adults without DS has been reported, the effect of gene dosage may be a contributing factor in reducing lipid peroxidation in obese adults with DS, without being a protective factor of its pathological consequences.

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