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Some Aspects of Liver Function Status in G6PD Deficient Neonates and Its Relationship with G6PD

机译:G6PD缺陷型新生儿肝功能状态的某些方面及其与G6PD的关系

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Neonatal jaundice is a common cause of newborn hospital admission. G6PD enzyme defects is one of the factor to develop neonatal hyperbilirubinemia, which may be related to abnormal liver function in this group of neonates.Objective: To observe some aspects of liver function status by measuring serum bilirubin and alanine amino transferase levels in G6PD deficient neonates and also their relationship with erythrocyte G6PD levels.Methods: The study was conducted on 30 male, term neonates with G6PD deficiency in the Department of Physiology, Bangabandhu Sheikh Mujib Medical University (BSMMU) between 1st July 2007 to 30th June 2008. For comparison age and sex matched 30 apparently healthy neonates without deficiency (control group) were also included in the study. Erythrocyte G6PD level was measured by Spectrophotometric method by using kit of Randox. Alanine amino transferase level was done by Schumann and Klauke method. For statistical analysis independent sample “t” test and Pearson’s correlation coefficient test were performed as applicable by using SPSS for windows version-13Results: In this study, significantly (p<0.001)higher level of serum bilirubin & ALT were found in G6PD deficient group in comparison to those of non-deficient group. Further more, serum bilirubin & ALT levels were negatively (r=-.671, (r= -.534) correlated with erythrocyte G6PD level and it was statistically significant (p<0.01) in G6PD deficient group. Again, significant (p<0.05) positive (r=+.429) correlation of serum bilirubin level was observed in non deficient group. Whereas, non significant positive (r=+.041) correlations of ALT was found in non deficient group.Conclusion: From the study results it can be concluded that higher level of alanine amino transferaseand hyperbilirubinemia were present in G6PD deficient neonates & increase serum bilirubin and serum alanine amino transferase levels were associated with degree of G6PD enzyme deficiency. DOI: http://dx.doi.org/10.3329/jbsp.v7i1.11158 J Bangladesh Soc Physiol. 2012, June; 7(1): 36-40
机译:新生儿黄疸是新生儿入院的常见原因。 G6PD酶缺陷是导致新生儿高胆红素血症的因素之一,可能与这一组新生儿的肝功能异常有关。目的:通过测量G6PD缺陷型新生儿的血清胆红素和丙氨酸氨基转移酶水平来观察肝功能状态的某些方面方法:该研究于2007年7月1日至2008年6月30日在班加班德谢赫穆吉布医科大学生理学系对30名G6PD缺乏的男性足月新生儿进行。与性别匹配的30例健康健康,无缺陷的新生儿(对照组)也包括在研究中。使用Randox试剂盒通过分光光度法测量红细胞G6PD水平。丙氨酸氨基转移酶水平通过Schumann和Klauke方法测定。为了进行统计分析,使用适用于Windows版本13的SPSS进行了独立的样本t检验和Pearson相关系数检验。结果:在本研究中,G6PD缺乏症组的血清胆红素和ALT显着(p <0.001)高相较于非缺乏组。此外,血清胆红素和ALT水平与红细胞G6PD水平呈负相关(r =-。671,(r = -.534),在G6PD缺乏组中有统计学意义(p <0.01)。非缺陷组血清胆红素水平为0.05)(r = +。429)呈正相关,而非缺陷组ALT中非显着(r = +。041)呈正相关。可以得出结论,G6PD缺乏的新生儿存在较高水平的丙氨酸氨基转移酶和高胆红素血症,血清胆红素和血清丙氨酸氨基转移酶水平升高与G6PD酶缺乏程度有关。DOI:http://dx.doi.org/10.3329 /jbsp.v7i1.11158 J Bangladesh Soc Physiol.2012年6月; 7(1):36-40

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