維持性血液透析患者心臟瓣膜鈣化影響因素的Meta分析
本文關(guān)鍵詞: 維持性血液透析 心臟瓣膜鈣化 影響因素 Meta分析 出處:《吉林大學(xué)》2017年碩士論文 論文類型:學(xué)位論文
【摘要】:背景:近20年來對慢性腎臟病(Chronic Kidney Disease,CKD)的深入研究,發(fā)現(xiàn)隨著腎功能下降其心腦血管疾病的發(fā)生風(fēng)險顯著增加,包括冠狀動脈疾病、心力衰竭、嚴(yán)重心律失常和猝死等。而心腦血管疾病是終末期腎病(End-Stage Renal Disease,ESRD)的首要死亡原因,占所有死因的50%以上。CKD患者的動脈鈣化及由此所致的血管硬化也是導(dǎo)致心血管疾病發(fā)生和發(fā)展的重要因素之一,其中包括心臟瓣膜鈣化(Cardiac Valve Calcification,CVC)。心臟瓣膜鈣化是瓣膜狹窄的重要原因,常常發(fā)生在主動脈瓣和二尖瓣,可以導(dǎo)致心臟瓣膜功能性失調(diào),引起瓣膜狹窄或者關(guān)閉不全,進(jìn)而導(dǎo)致血流動力學(xué)改變。雖然心臟瓣膜鈣化的發(fā)生率較動脈鈣化發(fā)生率低,但與腎功能正常人群相比,CKD患者心臟瓣膜鈣化發(fā)生率高出5-10倍。而且透析也是CKD患者心臟瓣膜鈣化的危險因素之一,無論是血液透析還是腹膜透析。CKD患者中透析者心臟瓣膜鈣化的發(fā)生率是非透析者的4-5倍,維持性血液透析(Maintenance Hemodialysis,MHD)患者發(fā)生心臟瓣膜鈣化更加普遍,且病變進(jìn)展更快。有關(guān)維持性血液透析患者心臟瓣膜鈣化的研究較多,但對于其發(fā)病機(jī)制及治療等問題仍有較大爭議。目前越來越多的證據(jù)表明,除了傳統(tǒng)的心血管危險因素之外,礦物質(zhì)代謝異常、炎癥反應(yīng)等也參與CVC的發(fā)生和發(fā)展。為了更全面地了解并掌握MHD患者心臟瓣膜鈣化發(fā)生的影響因素、發(fā)病機(jī)制等問題,據(jù)此本文檢索了近15年有關(guān)維持性血液透析患者心臟瓣膜鈣化的病例對照研究的相關(guān)文獻(xiàn)進(jìn)行Meta分析,為進(jìn)一步探討其治療及預(yù)防措施,最終降低MHD患者的死亡率并提高患者的生活質(zhì)量做基礎(chǔ)。目的:通過Meta分析探討維持性血液透析患者心臟瓣膜鈣化的影響因素。方法:基于觀察性研究的Meta分析規(guī)范(Meta-analysis Of Observational Studies in Epidemiology,MOOSE)聲明進(jìn)行研究及撰寫。計(jì)算機(jī)檢索Embas、Pubmed、Web of Sciences、中國知網(wǎng)、萬方、維普、CBMdisc等數(shù)據(jù)庫,收集2000年1月-2015年10月公開發(fā)表的有關(guān)維持性血液透析患者心臟瓣膜鈣化的影響因素的文獻(xiàn),并應(yīng)用Rev Man5.3軟件進(jìn)行Meta分析,Stata 13.0軟件進(jìn)行偏倚分析。結(jié)果:共納入16篇文獻(xiàn),共納入研究對象3061例,其中存在心臟瓣膜鈣化1541例,無心臟瓣膜鈣化1520例。Meta分析結(jié)果顯示:1)維持性血液透析患者心臟瓣膜鈣化與年齡增加[WMD=9.64,95%CI(7.75,11.52),P0.001]、血液透析時間增加[WMD=25.87,95%CI(15.90,35.83),P0.001]、血磷濃度更高[WMD=0.57,95%CI(0.22,0.92),P=0.001]、炎癥反應(yīng)中的C-反應(yīng)蛋白水平更高[WMD=3.13,95%CI(1.29,4.95),P0.001]、成纖維細(xì)胞生長因子-23水平更高[WMD=0.5,95%CI(0.21,0.79),P0.001]相關(guān),差異存在統(tǒng)計(jì)學(xué)意義(P0.01)。2)維持性血液透析患者心臟瓣膜鈣化與血清白蛋白水平降低[WMD=-0.88,95%CI(-1.41,-0.36),P=0.001]、胎球蛋白A水平降低[SMD=-1.24,95%CI(-1.83,-0.65),P0.001]具有相關(guān)性,差異存在統(tǒng)計(jì)學(xué)意義(P0.01)。結(jié)論:初步確定年齡、血液透析時間、血磷濃度、成纖維細(xì)胞生長因子-23、炎癥反應(yīng)中的C-反應(yīng)蛋白是影響維持性血液透析患者心臟瓣膜鈣化發(fā)生的重要危險因素,胎球蛋白A、血清白蛋白是維持性血液透析患者心臟瓣膜鈣化的保護(hù)性因素。
[Abstract]:Background: in the past 20 years of chronic kidney disease (Chronic Kidney, Disease, CKD) of the study, found that the risk of cardiovascular and cerebrovascular diseases with the decline in renal function increased significantly, including coronary artery disease, heart failure, arrhythmia and sudden death. The cardiovascular disease is the end-stage renal disease (End-Stage Renal Disease. ESRD) the primary cause of death, accounting for more than 50% of all deaths of arterial calcification in.CKD patients and thus induced vascular sclerosis is one of the important factors leading to the occurrence and development of cardiovascular disease, including heart valve calcification (Cardiac Valve, Calcification, CVC). Cardiac valve calcification is an important cause of valvular stenosis, often occurs in the aortic valve and the mitral valve, which can lead to cardiac valvular function disorder, caused by valvular stenosis or insufficiency, leading to hemodynamic changes. Although cardiac valve calcium The incidence of arterial calcification rate is low, but compared with the normal renal function group, CKD patients with heart valve calcification rate is 5-10 times higher. And is also one of the risk factors of dialysis patients with CKD cardiac valve calcification, whether hemodialysis or peritoneal dialysis in patients with.CKD. The analysis of heart valve calcification incidence 4-5 times of non dialysis, hemodialysis (Maintenance Hemodialysis, MHD) in patients with heart valve calcification is more prevalent, and the lesions progress faster. More research concerning the maintenance of cardiac valve calcification in hemodialysis patients, but for the pathogenesis and treatment of the problem is still controversial. At present more and more evidence that in addition to traditional cardiovascular risk factors, abnormal mineral metabolism, the occurrence and development of inflammatory reaction in CVC. In order to fully understand and master the MHD patients with heart Influence factors of valve calcification occurred, pathogenesis, so this paper retrieval literature comparative study of nearly 15 years concerning the maintenance of cardiac valve calcification in hemodialysis patients were analyzed by Meta, to further explore the treatment and preventive measures, and ultimately reduce the mortality of MHD patients and improve the patient's quality of life based. Through the Meta analysis to evaluate the effect of maintenance of cardiac valve calcification in hemodialysis patients. Methods: standard analysis of observational studies based on Meta (Meta-analysis Of Observational Studies in Epidemiology, MOOSE) to conduct research and write a statement. Retrieved from Embas, Pubmed, Web of Sciences, Chinese CNKI, Wanfang, VIP, CBMdisc and other databases. From January 2000 October -2015 published the effect of maintenance of cardiac valve calcification in hemodialysis patients and the factors of the literature. The application of Rev Man5.3 Meta analysis software, Stata 13 software for bias analysis. Results: a total of 16 articles were included, were included in the study of 3061 cases in which the presence of valvular calcification in 1541 cases, the results showed no cardiac valve calcification in 1520 cases of.Meta: 1) maintenance hemodialysis patients with heart valve calcification and age [WMD=9.64,95%CI (7.75,11.52, P0.001]), hemodialysis time increased by [WMD=25.87,95%CI (15.90,35.83), P0.001], serum phosphate concentration higher [WMD=0.57,95%CI (0.22,0.92), P=0.001], flat water C- reactive protein in inflammation, the higher [WMD=3.13,95%CI (1.29,4.95), P0.001], fibroblast growth factor -23 higher level of [WMD=0.5,95%CI (0.21,0.79), P0.001]. There were statistically significant differences (P0.01).2) in maintenance hemodialysis patients with heart valve calcification and serum albumin level decreased [WMD=-0.88,95%CI (-1.41, -0.36), P=0.001], Reduce the fetuin A level of [SMD=-1.24,95%CI (-1.83, -0.65), associated with P0.001], there were statistically significant differences (P0.01). Conclusion: to determine the initial age, dialysis time, blood phosphorus concentration, fibroblast growth factor -23, C- reaction protein in inflammation is to maintain an important risk of cardiac valve calcification in hemodialysis patients with blood factors, fetuin A, serum albumin is a protective factor of cardiac valve calcification in hemodialysis patients.
【學(xué)位授予單位】:吉林大學(xué)
【學(xué)位級別】:碩士
【學(xué)位授予年份】:2017
【分類號】:R692.5;R542.5
【相似文獻(xiàn)】
相關(guān)期刊論文 前10條
1 張玉慧,王威,段毅;老年性瓣膜鈣化的分析[J];臨床超聲醫(yī)學(xué)雜志;2001年S1期
2 楊波,王顯芝;老年男性心臟瓣膜鈣化相關(guān)因素分析[J];北京醫(yī)學(xué);2004年06期
3 司馬福;;高原老年人心臟瓣膜鈣化的相關(guān)因素分析[J];高原醫(yī)學(xué)雜志;2007年02期
4 孔祥清;;瓣膜鈣化的現(xiàn)代認(rèn)識[J];中國病理生理雜志;2010年10期
5 李云橋;汪金峰;彭雯;葛晶;;心臟瓣膜鈣化與增齡相關(guān)性改變[J];臨床心血管病雜志;2012年08期
6 何軍,姜楞;老年性心瓣膜鈣化的發(fā)病情況,易患因素的探討[J];聲學(xué)技術(shù);1991年03期
7 張麗,黃平,黃凌,唐安戊,黃新勝,肖建英;老年心臟瓣膜鈣化的病因探討[J];嶺南心血管病雜志;2000年02期
8 張良峰,徐巖,王昌會,程自平,朱潤碩,史學(xué)功,許邦龍,陳斌;老年心臟瓣膜鈣化的危險因素分析[J];臨床薈萃;2005年03期
9 Fox C.S.;Larson M.G. ;楊海濤;;炎癥、新的危險因素與瓣膜鈣化間的關(guān)系[J];世界核心醫(yī)學(xué)期刊文摘(心臟病學(xué)分冊);2006年10期
10 謝瑞濃;張?jiān)氯A;張珍萍;;老年退行性心臟瓣膜鈣化患者的護(hù)理[J];中國老年保健醫(yī)學(xué);2007年05期
相關(guān)會議論文 前6條
1 孔祥清;;瓣膜鈣化的現(xiàn)代認(rèn)識[A];中國病理生理學(xué)會第九屆全國代表大會及學(xué)術(shù)會議論文摘要[C];2010年
2 馬忠武;朱小敏;戴峰;趙立鶴;張瑋;馮娜;趙新國;;心臟瓣膜鈣化與冠心病的關(guān)系超聲研究[A];第二屆長三角超聲醫(yī)學(xué)論壇暨2009年浙江省超聲醫(yī)學(xué)學(xué)術(shù)年會論文匯編[C];2009年
3 馬忠武;趙新國;朱小敏;戴峰;趙立鶴;張瑋;馮娜;;心臟瓣膜鈣化與冠心病的關(guān)系超聲研究[A];2011年浙江省超聲醫(yī)學(xué)學(xué)術(shù)年會論文匯編[C];2011年
4 秦永彥;趙秀蓮;陶謙;;老年人心臟瓣膜鈣化與冠心病的關(guān)系[A];中華醫(yī)學(xué)會第六次全國超聲醫(yī)學(xué)學(xué)術(shù)年會論文匯編[C];2001年
5 羅艷;;彩色多普勒超聲心動圖檢測肝臟病變老年組心瓣膜退行性改變[A];第九屆全國超聲心動圖學(xué)術(shù)會議論文集[C];2007年
6 戎殳;葉朝陽;牛曉萍;高文武;梅長林;;尿毒癥血液透析患者心臟瓣膜鈣化及其危險因素[A];“中華醫(yī)學(xué)會腎臟病學(xué)分會2004年年會”暨“第二屆全國中青年腎臟病學(xué)術(shù)會議”論文匯編[C];2004年
相關(guān)重要報(bào)紙文章 前2條
1 程懷孟;易漏診的老年退行性心臟瓣膜病[N];家庭醫(yī)生報(bào);2008年
2 李仲英;半夜嗆咳不妨查查心臟[N];中國中醫(yī)藥報(bào);2000年
相關(guān)博士學(xué)位論文 前2條
1 王琳;社區(qū)老年人群退行性心臟瓣膜病的五年縱向研究[D];中國人民解放軍軍醫(yī)進(jìn)修學(xué)院;2011年
2 胡行健;組織工程化模型探討異常力學(xué)刺激誘導(dǎo)心臟瓣膜鈣化機(jī)制研究[D];華中科技大學(xué);2013年
相關(guān)碩士學(xué)位論文 前10條
1 王菊;慢性腎臟病3-5期患者血清25-羥維生素D_3水平影響因素分析及其與心臟瓣膜鈣化的相關(guān)性[D];安徽醫(yī)科大學(xué);2016年
2 王永濤;IL-10及apo-B基因多態(tài)性與心臟瓣膜鈣化的相關(guān)性研究[D];新疆醫(yī)科大學(xué);2016年
3 田云還;維持性腹膜透析患者新發(fā)瓣膜鈣化的危險因素及對預(yù)后的影響[D];蘇州大學(xué);2016年
4 張?jiān)聥?維持性血液透析患者心臟瓣膜鈣化影響因素的Meta分析[D];吉林大學(xué);2017年
5 黃正林;老年鈣化性心臟瓣膜病的相關(guān)危險因素及瓣膜鈣化與頸動脈粥樣硬化關(guān)系的病例對照研究[D];重慶醫(yī)科大學(xué);2008年
6 王春元;腹膜透析患者心臟瓣膜鈣化的危險因素及對預(yù)后的影響[D];蘇州大學(xué);2014年
7 龔林;老年單純收縮期高血壓患者動脈僵硬度與心臟瓣膜鈣化的相關(guān)性研究[D];昆明醫(yī)科大學(xué);2014年
8 劉靜;老年退行性心臟瓣膜病的臨床特點(diǎn)與相關(guān)因素分析[D];新疆醫(yī)科大學(xué);2010年
9 鐘笑偉;老年退行性心臟瓣膜病相關(guān)因素分析[D];大連醫(yī)科大學(xué);2006年
10 高峰;腹膜透析患者鈣磷代謝及心臟瓣膜鈣化的相關(guān)研究[D];大連醫(yī)科大學(xué);2007年
,本文編號:1451092
本文鏈接:http://www.wukwdryxk.cn/shoufeilunwen/mpalunwen/1451092.html