吳佳健+邱崇榮
摘要:目的 內(nèi)皮細(xì)胞特異性分子-1是近年來(lái)發(fā)現(xiàn)的新型內(nèi)皮功能紊亂生物標(biāo)記物,內(nèi)皮功能紊亂在冠心病發(fā)病過(guò)程中起了重要作用,本研究探討冠心病患者入院血清ESM-1表達(dá)水平及與冠狀動(dòng)脈病變及其嚴(yán)重程度的關(guān)系。方法 對(duì)130例行冠狀動(dòng)脈造影檢查患者,按造影結(jié)果分為冠心病組(70例)和對(duì)照組(非冠心病組,60例),對(duì)所有入組患者進(jìn)行血清ESM-1檢測(cè)。比較兩組患者血清ESM-1表達(dá)水平,同時(shí),對(duì)冠心病組中將不同亞組患者的血清ESM-1水平進(jìn)一步比較。結(jié)果 與對(duì)照組比較,冠心病組ESM-1水平較高[(1.31±0.72) ng/ml vs (1.09±0.14) ng/ml, P<0.05]、冠心病亞組中,多支血管病變者血清ESM-1水平明顯高于單支血管病變組,差異有統(tǒng)計(jì)學(xué)意義(P<0.05)。結(jié)論 冠心病患者血清ESM-1水平高于對(duì)照組,ESM-1可能是冠心病患者內(nèi)皮功能紊亂新型生物標(biāo)記物,其表達(dá)水平且隨血管病變程度加重而增高。
關(guān)鍵詞:冠心??;內(nèi)皮細(xì)胞特異性分子-1;生物標(biāo)記物
中圖分類(lèi)號(hào):R542.22 文獻(xiàn)標(biāo)識(shí)碼:A 文章編號(hào):1006-1959(2017)25-0179-02
Abstract:Objective Endothelial cell-specific molecule-1 is a new biomarker of endothelial dysfunction found in recent years.Endothelial dysfunction plays an important role in the pathogenesis of coronary heart disease.This study was to investigate the relationship between serum ESM-1 expression in patients with coronary heart disease and the severity of coronary artery disease.Methods 130 patients undergoing coronary angiography were divided into coronary heart disease group(70 cases)and control group(non-coronary heart disease group,60 cases)according to the results of angiography.Serum ESM-1 was detected in all patients.Serum ESM-1 levels were compared between the two groups,meanwhile,serum ESM-1 levels in different subgroups were further compared in CHD group.Results Compared with the control group,the ESM-1 level in CHD group was significantly higher than that in the control group[(1.31±0.72)ng/mL vs(1.09±0.14)ng/mL,P<0.05],In the coronary heart disease subgroup,the level of ESM-1 in the multivessel disease group was significantly higher than that in the single vessel disease group(P<0.05).Conclusion The level of serum ESM-1 in patients with coronary heart disease is higher than that in the control group.ESM-1 may be a new biomarker of endothelial dysfunction in patients with coronary heart disease.The level of ESM-1 expression is increased with the severity of vascular disease.
Key words:Coronary heart disease;Endothelial cell-specific molecule-1;Biomarker
隨著社會(huì)的進(jìn)步,人們生活方式改變,心血管疾病已經(jīng)成為全球主要死亡原因。其中動(dòng)脈粥樣硬化性疾病呈現(xiàn)出上升的趨勢(shì)[1]。內(nèi)皮功能紊亂是冠狀動(dòng)脈粥樣硬化性心臟病發(fā)病的始動(dòng)環(huán)節(jié)并貫穿于冠心病發(fā)病整個(gè)過(guò)程。冠心病與內(nèi)皮功能指標(biāo)的研究為當(dāng)前研究熱點(diǎn)之一,內(nèi)皮細(xì)胞特異性分子-1(Endothelial cell-specific molecule-1,ESM-1),主要由血管內(nèi)皮細(xì)胞分泌,可能是血管內(nèi)皮細(xì)胞功能紊亂的生物標(biāo)記物[2]。然而,關(guān)于ESM-1與冠心病患者冠狀動(dòng)脈病變的臨床研究國(guó)內(nèi)鮮見(jiàn)文獻(xiàn)報(bào)道。本研究探討冠心病與ESM-1水平之間的關(guān)系,從而對(duì)冠狀動(dòng)脈病變臨床意義進(jìn)行評(píng)估,為臨床診斷治療提供實(shí)驗(yàn)室依據(jù)。
1資料與方法
1.1一般資料
選擇2015年1月~2016年7月于本院住院行冠狀動(dòng)脈造影并被確診為冠心病的患者70例為冠心病組,其中男性40例,女性30例,平均年齡(63.67±12.07)歲;另選取60例行冠狀動(dòng)脈造影檢結(jié)果正常者為對(duì)照組,其中男性36例,女性24例,平均年齡(60.66±7.59)歲。endprint
1.2排除標(biāo)準(zhǔn)與納入標(biāo)準(zhǔn)
納入標(biāo)準(zhǔn):冠狀動(dòng)脈造影檢查證實(shí)管腔狹窄程度大于50%為冠心病組,冠狀動(dòng)脈造影檢查結(jié)果正常者為對(duì)照組。排除標(biāo)準(zhǔn):①血液系統(tǒng)疾??;②甲狀腺疾??;③免疫性疾??;④?chē)?yán)重瓣膜疾?。虎輫?yán)重腎功能不全(CKD 4期、CKD5期)需要腎透析治療;⑥自身免疫性疾?。虎吒腥拘约膊。虎鄲盒阅[瘤。
1.3方法
檢測(cè)血清ESM-1表達(dá)水平,所有研究對(duì)象抽取外周靜脈血,采用酶聯(lián)免疫法(ELSIA)檢測(cè)血清ESM-1表達(dá)水平,檢測(cè)步驟嚴(yán)格按照試劑盒說(shuō)明進(jìn)行。
1.4療效評(píng)價(jià)
比較冠心病組與對(duì)照組ESM-1表達(dá)水平差異性,并分析ESM-1水平與冠脈病變嚴(yán)重程度關(guān)系,為臨床診斷治療提供實(shí)驗(yàn)室依據(jù)。
1.3 統(tǒng)計(jì)學(xué)方法
應(yīng)用SPSS19.0軟件建立數(shù)據(jù)庫(kù)并進(jìn)行統(tǒng)計(jì)分析,計(jì)量資料用(x±s)表示,比較兩組均數(shù)差別有無(wú)統(tǒng)計(jì)學(xué)意義用t檢驗(yàn); P<0.05為差異有統(tǒng)計(jì)學(xué)意義。
2 結(jié)果
冠心病組與對(duì)照組及冠心病亞組血清ESM-1水平比較,冠心病組血清ESM-1水平明顯高于對(duì)照組高[(1.31±0.72)ng/ml vs (1.09±0.14)ng/ml,P<0.05],進(jìn)一步對(duì)冠心病亞組分析,發(fā)現(xiàn)冠心病多支血管病變患者血清ESM-1水平比單支血管病變明顯增高[(1.45±0.93)ng/ml vs (1.13±0.32)ng/ml,P<0.05)。
3 討論
多年來(lái)尋找簡(jiǎn)便可行的識(shí)別冠心病的指標(biāo)是心血管領(lǐng)域的重要工作之一。冠狀動(dòng)脈造影檢查雖為診斷冠心病的金標(biāo)準(zhǔn),但因其價(jià)格昂貴且為有創(chuàng)性檢查,因此其應(yīng)用受到限制。近年來(lái)一種反映內(nèi)皮功能紊亂的新型生物標(biāo)記物,內(nèi)皮細(xì)胞特異性分子-1,引起了學(xué)者們的關(guān)注。ESM-1,亦稱(chēng)Endocan,1996年由法國(guó)科學(xué)家Lassale等在對(duì)人臍靜脈內(nèi)皮細(xì)胞cDNA (complimentary DNA,互補(bǔ)DNA) 文庫(kù)中進(jìn)行克隆分離哮喘相關(guān)互補(bǔ)DNA序列而意外發(fā)現(xiàn)并首次報(bào)道[3-6]。其在體內(nèi)多種腫瘤的小血管和大血管內(nèi)皮基質(zhì)均有表達(dá),對(duì)調(diào)節(jié)細(xì)胞粘附、遷移、增殖起了重要作用。近年來(lái)有學(xué)者關(guān)注ESM-1與心血管疾病之間的關(guān)系,Menon等在動(dòng)物實(shí)驗(yàn)中發(fā)現(xiàn)ESM-1在粥樣斑塊中高表達(dá),推測(cè)ESM-1分泌增加可能促進(jìn)動(dòng)脈血管平滑肌 (Vascular smooth muscle,VSMC)的遷移和增殖,與動(dòng)脈硬化疾病關(guān)系密切[7-8]。
然而, ESM-1與冠心病患者冠狀動(dòng)脈病變的臨床研究目前國(guó)內(nèi)鮮見(jiàn)文獻(xiàn)報(bào)道,本研究檢測(cè)了冠心病組血清ESM-1水平并分析ESM-1與病變支數(shù)關(guān)系。
本研究觀察指標(biāo)ESM-1,通過(guò)收集血清標(biāo)本用ELSIA進(jìn)行檢測(cè),其損傷較小,檢測(cè)方法較為簡(jiǎn)單。具有較好的臨床應(yīng)用前景。
本研究發(fā)現(xiàn),ESM-1在冠心病患者中高表達(dá),提示其可能參與冠心病發(fā)病過(guò)程。本研究與既往相關(guān)研究結(jié)論一致[9-11]。本研究還發(fā)現(xiàn),隨病變支數(shù)增加,ESM-1水平亦呈上升趨勢(shì),說(shuō)明ESM-1水平增高是冠脈病變預(yù)測(cè)因子,且與血管病變程度呈正相關(guān)。
然而,目前關(guān)于ESM-1與冠狀動(dòng)脈病變程度關(guān)系的研究國(guó)內(nèi)鮮見(jiàn)文獻(xiàn)報(bào)道。本研究納入130例患者,其中冠心病患者ESM-1水平明顯高于對(duì)照組,且ESM-1水平隨冠脈病變程度的加重而升高。本研究提示ESM-1可能為冠心病患者新型內(nèi)皮功能紊亂生物標(biāo)記物,可能與冠心病相關(guān),可能是反映冠狀動(dòng)脈病變及嚴(yán)重程度的指標(biāo)之一,可作為冠脈病變的預(yù)測(cè)因子,這為冠心病的診斷及病情評(píng)估提供了新的無(wú)創(chuàng)性手段,具有一定的應(yīng)用前景。
參考文獻(xiàn):
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編輯/高章利endprint