[1]陈云华.肝脏疾病与内分泌代谢疾病的相关性[J].医学信息,2022,35(18):96-98.[doi:10.3969/j.issn.1006-1959.2022.18.025]
 CHEN Yun-hua.Correlation Between Liver Diseases and Endocrine Metabolic Diseases[J].Journal of Medical Information,2022,35(18):96-98.[doi:10.3969/j.issn.1006-1959.2022.18.025]
点击复制

肝脏疾病与内分泌代谢疾病的相关性()
分享到:

医学信息[ISSN:1006-1959/CN:61-1278/R]

卷:
35卷
期数:
2022年18期
页码:
96-98
栏目:
临床研究
出版日期:
2022-09-15

文章信息/Info

Title:
Correlation Between Liver Diseases and Endocrine Metabolic Diseases
文章编号:
1006-1959(2022)18-0096-03
作者:
陈云华
(遂宁市第三人民医院内三科,四川 遂宁 629000)
Author(s):
CHEN Yun-hua
(The Third Department of Internal Medicine,Suining Third People’s Hospital,Suining 629000,Sichuan,China)
关键词:
肝脏疾病内分泌代谢肝损害肝功能
Keywords:
Liver diseaseEndocrine metabolismLiver damageLiver function
分类号:
R58;R57
DOI:
10.3969/j.issn.1006-1959.2022.18.025
文献标志码:
A
摘要:
目的 研究肝脏疾病与内分泌代谢疾病的相关性。方法 选取2020年7月-2021年7月在我院诊治的122例内分泌代谢疾病患者为研究对象,其中2型糖尿病38例,甲状腺功能亢进26例,肾功能衰竭30例,性功能障碍28例,另选取同期体检健康者120名为对照组,比较各疾病患者及对照组肝功能指标水平、肝功能异常发生率、合并肝脏疾病发生率、预后及转归。结果 2型糖尿病、甲状腺功能亢进、肾功能衰竭、性功能障碍患者血清丙氨酸氨基转移酶(ALT)、天门冬氨酸氨基转移酶(AST)、谷氨酰基转移酶(GGT)水平均高于对照组(P<0.05);甲状腺功能亢进、肾功能衰竭患者肝功能异常发生率高于2型糖尿病、性功能障碍患者,且肾功能衰竭患者肝功能异常发生率高于甲状腺功能亢进患者(P<0.05);2型糖尿病、性功能障碍患者肝功能异常发生率比较,差异无统计学意义(P>0.05);肾功能衰竭患者合并肝脏疾病发生率高于2型糖尿病、甲状腺功能亢进、性功能障碍患者,甲状腺功能亢进患者合并肝脏疾病发生率高于2型糖尿病、性功能障碍患者(P<0.05);Pearson相关性分析显示,内分泌代谢疾病患者合并肝脏疾病发生率与肝功能指标水平呈正相关(P<0.05),与肝功能异常发生率无相关性(P>0.05)。结论 肝脏疾病与内分泌代谢具有一定的关系,可与肝脏疾病共同存在,肝脏疾病会增加肝功能损害,临床在治疗内分泌代谢疾病的同时,应辅以保肝治疗,使患者随着病情的好转肝功能逐渐恢复正常,进一步改善预后。
Abstract:
Objective To study the correlation between liver diseases and endocrine and metabolic diseases.Methods A total of 122 patients with endocrine and metabolic diseases diagnosed and treated in our hospital from July 2020 to July 2021 were selected as the study subjects, including 38 patients with type 2 diabetes, 26 patients with hyperthyroidism, 30 patients with renal failure, and 28 patients with sexual dysfunction. Another 120 healthy subjects who underwent physical examination during the same period were selected as the control group. The levels of liver function indexes, the incidence of abnormal liver function, the incidence of combined liver disease, prognosis and outcome were compared between the patients with various diseases and the control group.Results The levels of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and glutamyl transferase (GGT) in patients with type 2 diabetes, hyperthyroidism, renal failure and sexual dysfunction were higher than those in control group (P<0.05). The incidence of abnormal liver function in patients with hyperthyroidism and renal failure was higher than that in patients with type 2 diabetes and sexual dysfunction, and the incidence of abnormal liver function in patients with renal failure was higher than that in patients with hyperthyroidism (P<0.05). There was no significant difference in the incidence of abnormal liver function between patients with type 2 diabetes and sexual dysfunction (P>0.05). The incidence of liver disease in patients with renal failure was higher than that in patients with type 2 diabetes, hyperthyroidism and sexual dysfunction, and the incidence of liver disease in patients with hyperthyroidism was higher than that in patients with type 2 diabetes and sexual dysfunction (P<0.05). Pearson correlation analysis showed that the incidence of liver disease in patients with endocrine and metabolic diseases was positively correlated with the level of liver function (P<0.05), but not with the incidence of abnormal liver function (P>0.05).Conclusion Liver disease has a certain relationship with endocrine metabolism, which can coexist with liver disease. Liver disease will increase liver function damage. Clinical treatment of endocrine and metabolic diseases should be supplemented by liver protection treatment, so that patients can gradually return to normal liver function with the improvement of the disease, and further improve the prognosis.

参考文献/References:

[1]朱凡凡,仰礼真.甲状腺功能正常的2型糖尿病患者血清甲状腺激素水平与非酒精性脂肪性肝病的相关性[J].上海交通大学学报(医学版),2018,38(7):763-768.[2]陈志惠,张世荣,孙文静,等.非酒精性脂肪性肝病患者肺功能变化临床分析[J].临床肝胆病杂志,2018,34(4):825-828.[3]Sinn DH,Kang D,Chang Y,et al.Non-alcoholic fatty liver disease and progression of coronary artery calcium score: a retrospective cohort study[J].Gut,2017,66(2):323-329.[4]张珊,张洁,傅力,等.2型糖尿病患者血清脂联素与肝脏脂肪含量的相关性研究[J].国际内分泌代谢杂志,2017,37(3):155-158.[5]中华医学会肝病学分会脂肪肝和酒精性肝病学组,中国医师协会脂肪性肝病专家委员会.非酒精性脂肪性肝病防治指南(2018年更新版)[J].实用肝脏病杂志,2018,21(2):177-186.[6]满冬亮,王齐晖.不同肝脏疾病血清GP73、AFP-L3、AFP及AFU水平的表达[J].肝脏,2016,21(5):368-371.[7]朱萍,卫红艳,王坤玲,等.Graves病甲状腺功能亢进症性肝损害的相关因素分析[J].国际内分泌代谢杂志,2017,37(3):164-167,217.[8]Ding Y,Xing J,Fang Y,et al.131I therapy for 345 patients with refractory severe hyperthyroidism: without antithyroid drug pretreatment [J].Exp Biol Med(Maywood),2016,241(3):290-295.[9]张庆,张伦理,向天新,等.人工肝系统联合131I治疗甲状腺功能亢进症合并肝衰竭研究[J].中华肝脏病杂志,2016,24(10):778-782.[10]钟筑宁,罗丽丽,肖文革,等.关于甲亢患者肝功能异常的临床观察[J].贵州医药,2017,41(3):289-290.[11]景良洪,陈琼科,宋凤萍,等.甲巯咪唑联合穴位敷贴治疗贴对甲状腺功能亢进症患者激素水平及骨代谢指标的影响[J].中国药房,2017,28(21):2905-2908.[12]马小陶,林兵,于永超,等.营养治疗对代谢综合征标准的2型糖尿病患者的效果研究[J].医学研究杂志,2016,45(8):70-73.[13]刘婷,王臣廷,刘美晓,等.2型糖尿病合并非酒精性脂肪性肝病患者肝纤维化与血尿酸水平的关系[J].临床肝胆病杂志,2020,36(6):1320-1324[14]Morling JR,Fallowfield JA,Guha IN,et al.Clinically significant chronic liver disease in people with type 2 diabetes: the Edinburgh Type 2 Diabetes Study[J].QJM,2016,109(4):249-256.[15]张正,孙中明,张芹,等.2型糖尿病人群肝功能异常影响因素分析[J]中国慢性病预防与控制,2017,25(2):81-84.[16]商书霞,宋光耀,刘晓耕,等.血清胆红素及γ-谷氨酰转肽酶与糖尿病患者非酒精性脂肪肝的相关性研究[J].徐州医学院学报,2017,37(4):245-247.

相似文献/References:

[1]张远明,王 丽.内分泌代谢领域4种期刊的文献计量学分析[J].医学信息,2019,32(05):25.[doi:10.3969/j.issn.1006-1959.2019.05.010]
 ZHANG Yuan-ming,WANG Li.Bibliometric Analysis of Four Journals in the Field of Endocrine Metabolism[J].Journal of Medical Information,2019,32(18):25.[doi:10.3969/j.issn.1006-1959.2019.05.010]
[2]李宏彬,贺太平.种决策树同源算法在肝部B超计算机辅助诊断中的应用比较[J].医学信息,2021,34(19):13.[doi:10.3969/j.issn.1006-1959.2021.19.003]
 LI Hong-bin,HE Tai-ping.Comparison of Three Decision Tree Homology Algorithms in ComputerAided Diagnosis of Liver B Ultrasound[J].Journal of Medical Information,2021,34(18):13.[doi:10.3969/j.issn.1006-1959.2021.19.003]

更新日期/Last Update: 1900-01-01