?

自發性急性腦出血患者血漿sCD163/sTWEAK比值與預后的關系

2024-04-01 10:57張文超楊雪輝尹濤王睿健張盟盟
天津醫藥 2024年3期
關鍵詞:比值血腫腦出血

張文超 楊雪輝 尹濤 王睿健 張盟盟

摘要:目的 探究自發性急性腦出血(ACH)患者血漿可溶性CD163(sCD163)/可溶性腫瘤壞死因子樣凋亡弱誘導因子(sTWEAK)比值與預后的關系。方法 納入ACH患者90例作為病例組,根據格拉斯哥預后評分將病例組分為預后不良組(38例)和預后良好組(52例);另選取同期體檢健康者45例為對照組。酶聯免疫吸附試驗檢測血漿sCD163、sTWEAK水平并計算sCD163/sTWEAK比值。分析血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值與臨床資料的相關性;Logistic回歸分析ACH患者預后不良的影響因素;受試者工作特征(ROC)曲線分析sCD163/sTWEAK比值對ACH患者預后不良的預測價值。結果 病例組血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值均顯著高于對照組;預后良好組上述指標均低于預后不良組(P<0.05)。預后良好組血腫體積、美國國立衛生研究院卒中量表(NIHSS)評分、高血壓及幕下出血比例均低于預后不良組,低密度脂蛋白膽固醇(LDL-C)高于預后不良組(P<0.05)。相關性分析表明,血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值與出血部位、血腫體積、NIHSS評分、白細胞計數、血小板計數、中性粒細胞/淋巴細胞比值(NLR)呈正相關(P<0.05)。Logistic回歸分析顯示,sCD163/sTWEAK比值、出血部位、血腫體積、NIHSS評分為ACH患者預后不良的影響因素(P<0.05)。ROC曲線結果表明,sCD163/sTWEAK比值評估ACH患者預后不良的AUC為0.850,敏感度和特異度分別為86.84%和69.23%。結論 sCD163/sTWEAK比值在ACH患者血漿中水平較高,并與預后不良有關,該值對此類患者的預后有一定預測價值。

關鍵詞:腦出血;細胞因子TWEAK;預后;可溶性血紅蛋白清道夫受體163蛋白;可溶性腫瘤壞死因子樣凋亡弱誘導因子

中圖分類號:R743.34文獻標志碼:ADOI:10.11958/20231437

The relationship between plasma sCD163/sTWEAK ratio and prognosis in patients with spontaneous acute cerebral hemorrhage

ZHANG Wenchao1, YANG Xuehui1△, YIN Tao2, WANG Ruijian2, ZHANG Mengmeng2

1 Department of Neurosurgery, Harison International Peace Hospital, Hengshui 053000, China;

2 Department of Neurosurgery, Hengshui People's Hospital

△Corresponding Author E-mail: Yxh1069@163.com

Abstract: Objective To investigate the relationship between the ratio of soluble hemoglobin scavenger receptor 163 protein (sCD163)/soluble tumor necrosis factor-like weak inducer of apoptosis (sTWEAK) in plasma and prognosis in patients with spontaneous acute cerebral hemorrhage (ACH). Methods From August 2020 to August 2022, 90 patients with ACH? admitted to the Department of Neurosurgery, Harison International Peace Hospital, Hengshui City were regarded as the research group. According to the Glasgow outcome scale, patients with ACH were separated into the poor prognosis group (n=38) and the good prognosis group (n=52). Another 45 healthy examinee who underwent physical examination were used as the control group. Enzyme linked immunosorbent assay (ELISA) was applied to detect plasma sCD163 and sTWEAK levels, and the sCD163/sTWEAK ratio was calculated. Pearson method was applied to analyze the correlation between plasma sCD163, sTWEAK levels, sCD163/sTWEAK ratio and clinical data. Logistic regression was applied to analyze influencing factors of poor prognosis in patients with ACH. Receiver operating characteristic (ROC) was applied to analyze the predictive value of sCD163/sTWEAK ratio for poor prognosis of patients with ACH. Results The plasma levels of sCD163, sTWEAK and sCD163/sTWEAK ratio were obviously higher in the research group than those in the control group (P<0.05). The plasma levels of sCD163, sTWEAK and sCD163/sTWEAK ratio were obviously lower in the good prognosis group than those in the poor prognosis group (P<0.05). Hematoma volume, National Institutes of Health Stroke Scale (NIHSS) scores, hypertension and subtentorial hemorrhage were lower in the good prognosis group than those in the poor prognosis group, and low density lipoprotein cholesterol (LDL-C) was higher in the good prognosis group than that in the poor prognosis group (P<0.05). Correlation analysis showed that plasma sCD163, and sTWEAK levels and the sCD163/sTWEAK ratio were positively correlated with bleeding site, hematoma volume, NIHSS score, white blood cell count, platelet count and neutrophil/lymphocyte ratio (NLR) (P<0.05). Results of Logistic regression analysis showed that sCD163, sTWEAK, sCD163/sTWEAK ratio, hematoma volume, bleeding site and NIHSS score were influencing factors for poor prognosis in patients with ACH (P<0.05). Results of receiver operating characteristic showed that the AUC of sCD163/sTWEAK ratio in evaluating poor prognosis of patients with ACH was 0.850, and the sensitivity and specificity were 86.84% and 69.23%. Conclusion The sCD163/sTWEAK ratio has a high level in the plasma of patients with ACH, which is associated with poor prognosis and has important value in predicting the prognosis of patients with ACH.

Key words: cerebral hemorrhage; cytokine TWEAK; prognosis; soluble hemoglobin scavenger receptor 163 protein; soluble tumor necrosis factor-like weak inducer of apoptosis

腦出血是腦卒中最常見的類型,其早期死亡和長期殘疾的風險較高[1]。自發性腦出血常由小血管疾病引起,包括深穿支動脈病變或腦淀粉樣血管??;盡管自發性腦出血占所有卒中的比例較低,但其導致卒中發病率和死亡率的比例較高,且很少有經過驗證有效的急性或預防性治療方法[2]。血紅蛋白清道夫受體163蛋白(CD163)是單核細胞和巨噬細胞上的血紅蛋白清除受體,與炎癥有關,被認為是活化的M2巨噬細胞的標志物,在炎癥反應中上調,能促進血管生成和基質金屬蛋白酶的產生,可溶性CD163(soluble CD163,sCD163)通過膜蛋白的蛋白水解和外結構域分解釋放到血漿中,在炎癥期間,病原體和損傷相關的刺激會誘導sCD163脫落[3-4]??扇苄阅[瘤壞死因子樣凋亡弱誘導因子(soluble tumor necrosis factor‐like weak inducer of apoptosis,sTWEAK)是TNF超家族的細胞因子,能改變血腦屏障通透性,誘導基質金屬蛋白酶和促炎細胞因子在大腦中過表達,與血管內皮功能障礙、神經血管病變和心腦血管預后密切相關,在腦出血患者體內水平升高[5]。sCD163能與sTWEAK相互作用,sCD163/sTWEAK比值與C反應蛋白水平顯著相關,是各種疾病中比單獨sCD163和sTWEAK水平更顯著的預測因子[6]。但目前關于sCD163/sTWEAK比值與急性腦出血(acute cerebral hemorrhage,ACH)患者預后關系的研究相對較少。鑒于此,本研究主要分析ACH患者血漿sCD163/sTWEAK比值與預后的關系。

1 對象與方法

1.1 研究對象 選取衡水市哈勵遜國際和平醫院神經外科2020年8月—2022年8月收治的ACH患者90例并作為病例組,平均年齡(43.51±6.25)歲,男51例,女39例。納入標準:(1)符合《中國腦出血診治指南(2019)》診斷標準[7]。(2)進行了影像學檢查。(3)首次發病。(4)在發病12 h內入院接受治療。(5)臨床資料完整。排除標準:(1)腦梗死、腦腫瘤等。(2)神經系統疾病。(3)凝血功能障礙。(4)免疫系統紊亂。(5)進行過相關治療。(6)臟器功能障礙。另選取同期體檢健康者45例為對照組;平均年齡(42.87±6.11)歲,男25例,女20例。2組年齡(t=0.569)、性別(c2=0.015)比較差異無統計學意義(均P>0.05)。本研究經醫院倫理委員會批準(倫理號:2022-2-037-1),患者對研究內容知情并同意。

1.2 方法

1.2.1 血漿sCD163、sTWEAK水平測定 采集所有受試者入院24 h內空腹靜脈血5 mL,乙二胺四乙酸抗凝處理,1 000 r/min離心15 min分離血漿。酶聯免疫吸附試驗(試劑盒購自上海江萊生物科技有限公司)檢測血漿sCD163和sTWEAK水平,實驗具體操作按試劑盒說明進行。計算sCD163/sTWEAK比值。

1.2.2 臨床資料收集及預后隨訪 收集患者性別、年齡、體質量指數(BMI)、糖尿病、冠心病、高血壓、入院時血腫體積、出血部位、血壓、血糖、總膽固醇(TC)、三酰甘油(TG)、發病至手術時間、手術時間、白細胞計數(WBC)、低密度脂蛋白膽固醇(LDL-C)、血小板計數(PLT)、中性粒細胞/淋巴細胞比值(NLR)、美國國立衛生研究院卒中量表(NIHSS)評分等資料。在對患者隨訪3個月后,通過格拉斯哥預后評分(GOS)評估預后[8],根據GOS將病例組分為預后不良組(GOS≤3分)38例和預后良好組(GOS>3分)52例。

1.3 統計學方法 采用SPSS 25.0處理數據,計數資料以例(%)表示,組間比較采用χ2檢驗;計量資料以[x] ±s表示,組間比較采用t檢驗。Pearson法分析血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值與血腫體積、NIHSS評分、WBC、PLT、NLR的相關性,Spearman法分析與出血部位的相關性;Logistic回歸分析ACH患者預后不良的影響因素;受試者工作特征(ROC)曲線分析sCD163/sTWEAK比值對ACH患者預后不良的預測價值。P<0.05為差異有統計學意義。

2 結果

2.1 病例組和對照組血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值比較 病例組血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值均顯著高于對照組(P<0.05),見表1。

2.2 預后良好組和預后不良組血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值比較 預后良好組患者血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值顯著低于預后不良組患者(P<0.05),見表2。

2.3 2組患者臨床資料比較 預后良好組和預后不良組患者性別、年齡、BMI、糖尿病、冠心病、發病至手術時間、手術時間、TC、TG、收縮壓、舒張壓、血糖比較差異無統計學意義(P>0.05),預后良好組血腫體積、NIHSS評分、WBC、PLT、NLR、高血壓及幕下出血比例低于預后不良組,LDL-C高于預后不良組(P<0.05),見表3。

2.4 sCD163/sTWEAK與出血部位等指標的相關性分析 相關性分析表明,病例組血漿sCD163、sTWEAK水平及sCD163/sTWEAK比值與出血部位、血腫體積、NIHSS評分、WBC、PLT、NLR均呈正相關(P<0.05),見表4。

2.5 ACH患者預后不良的影響因素分析 sCD163、sTWEAK及sCD163/sTWEAK比值存在共線性,因此選擇以sCD163/sTWEAK比值、高血壓、WBC、血腫體積、PLT、LDL-C、NLR、NIHSS評分(均為實測值)、出血部位(幕下出血=1,幕上出血=0)為自變量,以ACH患者預后狀況為因變量(不良=1,良好=0),采用逐步向前法進行Logistic回歸分析。結果顯示,sCD163/sTWEAK比值、出血部位、血腫體積、NIHSS評分為ACH患者預后不良的影響因素(P<0.05),見表5。

2.6 sCD163、sTWEAK及sCD163/sTWEAK比值對ACH患者預后不良的預測價值 ROC曲線分析結果顯示,最佳截斷值為1.43×103時,sCD163/sTWEAK比值評估患者預后不良的敏感度和特異度更好,見表6、圖1。

3 討論

3.1 ACH的治療現狀 腦出血占所有急性腦血管事件的10%~30%,致殘率和死亡率較高,血腫可引發早期炎癥反應,從而增強出血性腦內損傷[9]。ACH患者可能出現血腫擴張、神經功能障礙等癥狀,與患者預后密切相關[10]。自發性腦出血預后較差,且受多種因素影響,近年來盡管此類患者的急性期管理取得了重大進展,但目前尚無特定治療方法能改善臨床結果和遠期結局[11]。因此,尋找合適的血漿指標對早期評估ACH患者預后可能具有重要意義。而本文通過檢測患者血漿sCD163、sTWEAK水平并計算sCD163/sTWEAK比值來分析其與ACH患者預后的關系。

3.2 sCD163與ACH的發生及預后的關系 CD163是單核巨噬細胞的清道夫受體,與炎癥反應有關;sCD163由膜蛋白的蛋白水解產生,以可溶形式釋放到血清或其他體液中,其水平升高與癌癥患者預后不良有關[12]。有研究表明,血清sCD163水平是巨噬細胞活性的標志物,具有抗炎活性和免疫調節作用,其水平上調可引起巨噬細胞活化和增殖,對活化T淋巴細胞的產生和增殖具有直接抑制作用;sCD163水平的升高可能是炎癥增加的標志,其在缺血性和出血性腦卒中的繼發性損傷中具有重要作用[13]。Drieu等[14]研究表明,CD163在腦脊液-動脈液流循環中起到關鍵作用,腦脊液循環不暢與腦出血后顱內壓升高、鐵離子神經元毒性等不良預后因素有關。ACH患者血清sCD163水平顯著高于健康人群,其水平與血腫擴張有關,血清sCD163高表達可促進ACH患者血腫吸收,可作為ACH患者不良結局的預后標志物[15]。在本研究中,ACH患者血漿sCD163水平顯著升高,預后良好患者sCD163水平低于預后不良者,說明sCD163水平與ACH患者預后可能具有一定關系。

3.3 sTWEAK及sCD163/sTWEAK與ACH發生及預后的關系 sTWEAK在單核細胞和內皮細胞中均有表達,能與跨膜Ⅰ型蛋白Fn14受體結合,導致信號通路的刺激和促炎分子的釋放,與腦出血患者早期血腫生長有關,可作為預測腦出血發生和腦出血患者不良功能結局的生物標志物[16]。有研究表明蛛網膜下腔出血患者血清sTWEAK水平較高,與炎癥和出血嚴重程度密切相關,其濃度升高可能造成患者不良臨床結局[17]。在本研究中,ACH患者血漿sTWEAK水平較高,且預后良好患者顯著低于預后不良者,說明sTWEAK水平可能與ACH患者預后有關。劉瑩等[18]研究表明,腦梗死后血清sTWEAK水平較高,其高水平會加重缺血后腦損傷。趙賓等[19]研究表明,血清sTWEAK水平與急性腦梗死患者腦白質病變密切相關,且其水平隨病變程度增加而上調。Altintas等[20]研究表明,心肌梗死預后不良患者sCD163、sTWEAK水平較高,sCD163與sTWEAK水平呈正相關。sCD163/sTWEAK比值增加與心腦血管疾病和外周動脈疾病嚴重程度和遠期死亡率有關[21]。本研究中,病例組sCD163/sTWEAK比值較高,預后良好組sCD163/sTWEAK較低。Logistic回歸分析表明sCD163/sTWEAK比值與ACH患者預后關系密切。ROC曲線結果表明,sCD163/sTWEAK比值對ACH患者預后不良具有良好的預測價值,進一步證實了該比值在ACH患者預后評估中的作用。

綜上所述,sCD163/sTWEAK比值在ACH患者血漿中水平較高,與患者預后不良有關,對預測ACH患者預后具有一定價值。但目前關于sCD163/sTWEAK比值與ACH患者預后關系的研究相對較少,且本研究中樣本量較小,隨訪時間較短,限制了研究結論普遍性,后續需增加樣本量深入研究。

參考文獻

[1] 張昆龍,薛白潔,肖瑋,等. 重復經顱磁刺激對神經病理性疼痛患者疼痛和情緒的影響[J]. 中國現代神經疾病雜志,2022,22(11):940-947. ZHANG K L,XUE B J,XIAO W,et al. Effects of repetitive transcranial magnetic stimulation on pain and emotion of patients with neuropathic pain[J]. Chin J Contemp Neurol Neurosurg,2022,22(11):940-947. doi:10.3969/j.issn.1672-6731.2022.11.005.

[2] HOSTETTLER I C,SEIFFGE D J,WERRING D J. Intracerebral hemorrhage:an update on diagnosis and treatment[J]. Expert Rev Neurother,2019,19(7):679-694. doi:10.1080/14737175.

2019.1623671.

[3] STUHR L K,MADSEN K,JOHANSEN A Z,et al. Combining sCD163 with CA 19-9 increases the predictiveness of pancreatic ductal adenocarcinoma[J]. Cancers (Basel),2023,15(3):897. doi:10.3390/cancers15030897.

[4] NIELSEN M C,HVIDBIERG G R,CLARIA J,et al. Macrophage activation markers,CD163 and CD206,in acute-on-chronic liver failure[J]. Cells,2020,9(5):1175. doi:10.3390/cells9051175.

[5] DA SILVA-CANDAL A,CUSTODIA A,L?PEZ-DEQUIDT I,et al. sTWEAK is a leukoaraiosis biomarker associated with neurovascular angiopathy[J]. Ann Clin Transl Neurol,2022,9(2):171-180. doi:10.1002/acn3.51502.

[6] SCS?NBAUER R,LICHTENAUER M,PAAR V,et al. Regular training increases sTWEAK and its decoy receptor sCD163-does training trigger the sTWEAK/sCD163-axis to induce an anti-inflammatory effect?[J]. J Clin Med. 2020,9(6):1899. doi:10.3390/jcm9061899.

[7] 中華醫學會神經病學分會,中華醫學會神經病學分會腦血管病學組. 中國腦出血診治指南(2019)[J]. 中華神經科雜志,2019,52(12):994-1005. Chinese Medical Association Branch of Neurology,Group of Cerebrovascular diseases, Branch of Neurology,Chinese Medical Association. Chinese Guidelines for Diagnosis and Treatment of cerebral hemorrhage(2019)[J]. Chinese Journal of Neurology,2019,52(12):994-1005. doi:10.3760/cma.j.issn.1006-7876.2019.12.003.

[8] 駱金輪,吳非,祝東強,等. 血清HMGB-1 MIF PDGF預測急性腦出血短期預后的臨床價值[J]. 河北醫學,2021,27(5):785-789. LUO J L,WU F,ZHU D Q,et al. Clinical value of serum HMGB-1 MIF PDGF in predicting short-term prognosis of acute cerebral hemorrhage[J]. Journal of Hebei Medical Sciences,2019,27(5):785-789. doi:10.3969/j.issn.1006-6233.2021.05.018.

[9] LATTANZI S,BRIGO F,TRINKA E,et al. Neutrophil-to-lymphocyte ratio in acute cerebral hemorrhage:a system review[J]. Transl Stroke Res,2019,10(2):137-145. doi:10.1007/s12975-018-0649-4.

[10] 王丹丹,王學建,潘南南. CT島征和黑洞征及其聯合征象對原發性腦出血早期血腫擴大的預測價值[J]. 天津醫藥,2021,49(2):199-202. WANG D D,WANG X J,PAN N N. The prognostic value of CT island sign,black hole sign and their combined signs for the hematoma enlargement in patients with early stage of primary intracerebral hemorrhage [J]. Tianjin Med J,2021,49(2):199-202. doi:10.11958/20200831.

[11] OLIVEIRA M A L. Surgery for spontaneous intracerebral hemorrhage[J]. Crit Care,2020,24(1):45. doi:10.1186/s13054-020-2749-2.

[12] QIAN S,ZHANG H,DAI H,et al. Is sCD163 a clinical significant prognostic value in cancers? a systematic review and meta-analysis[J]. Front Oncol,2020,10:585298. doi:10.3389/fonc.2020.585297.

[13] BHATTACHARYA A,ASHOURI R,FANGMAN M,et al. Soluble receptors affecting stroke outcomes:potential biomarkers and therapeutic tools[J]. Int J Mol Sci,2021,22(3):1108. doi:10.3390/ijms22031108.

[14] DRIEU A,DU S,STORCK S E,et al. Parenchymal border macrophages regulate the flow dynamics of the cerebrospinal fluid[J]. Nature,2022,611(7936):585-593. doi:10.1038/s41586-022-05397-3.

[15] 王靖萱,陳丹陽,王佳慧,等. 血清炎性標志物在腦出血預后評估中的作用研究進展[J]. 神經損傷與功能重建,2022,17(12):785-787. WANG J X,CHEN D Y,WANG J H,et al. The role of serum inflammatory markers in prognosis evaluation of cerebral hemorrhage[J]. Nerve Injury and Functional Reconstruction,2022,17(12):785-787. doi:10.16780/j.cnki.sjssgncj.20220909.

[16] SILVA-CANDAL A,LOPEZ-DEQUIDT I,RODRIGUEZ-YANEZ M,et al. sTWEAK is a marker of early haematoma growth and leukoaraiosis in intracerebral haemorrhage[J]. Stroke Vasc Neurol,2021,6(4):528-535. doi:10.1136/svn-2020-000684.

[17] DAI J X,CAI J Y,SUN J,et al. Serum soluble tumor necrosis factor-like weak inducer of apoptosis is a potential biomarker for outcome prediction of patients with aneurysmal subarachnoid hemorrhage[J]. Clin Chim Acta,2020,510(1):354-359. doi:10.1016/j.cca.2020.07.052.

[18] 劉瑩,王力娜,崔麗麗,等. TWEAK,NF-κB在腦梗死大鼠腦組織的表達及氧化苦參堿對其表達的影響[J]. 腦與神經疾病雜志,2020,28(3):137-143. LIU Y,WANG L N,CUI L L,et al. TWEAK,expression of NF-κB in brain tissue of rats with cerebral infarction and effect of oxymatrine on its expression [J]. Journal of Brain and Neurological Diseases,2020,28(3):137-143. doi:CNKI:SUN:LYSJ.0.2020-03-002.

[19] 趙賓,史肖錦,鐘平. 急性腦梗死患者早期血清腫瘤壞死因子樣弱凋亡誘導劑水平與腦白質病變的相關性[J]. 卒中與神經疾病,2021,28(1):54-57. ZHAO B,SHI X J,ZHONG P. Correlation between serum levels of tumor necrosis factor-like weak apoptosis inducer and white matter lesions in patients with acute cerebral infarction [J]. Stroke and Neurological Diseases,2021,28(1):54-57.

[20] ALTINTAS M S,EYERCI N,KARAYIGIT O,et al. Low sCD163/TWEAK ratio at first day after acute myocardial infarction associated with adverse cardiac remodeling in non-elderly patients[J]. Kardiologiia,2022,62(10):49-55. doi:10.18087/cardio.2022.10.n2155.

[21] MRAK D,ZIERFUSS B,HOBAUS C,et al. Evaluation of sCD163 and sTWEAK in patients with stable peripheral arterial disease and association with disease severity as well as long-term mortality[J]. Atherosclerosis,2021,317(1):41-46. doi:10.1016/j.atherosclerosis.2020.11.026.

(2023-10-07收稿 2023-11-30修回)

(本文編輯 李鵬)

猜你喜歡
比值血腫腦出血
中西醫結合治療腦出血的療效觀察
頭皮血腫不妨貼敷治
比值遙感蝕變信息提取及閾值確定(插圖)
慢性硬膜下血腫術后血腫復發的相關因素研究
脾切除后伴發腦出血1例并文獻復習
納洛酮在腦出血治療中的應用探析
不同應變率比值計算方法在甲狀腺惡性腫瘤診斷中的應用
問題2:老年患者中硬膜外血腫的手術指征?
雙電機比值聯動控制系統
腦出血早期血腫擴大的研究進展
91香蕉高清国产线观看免费-97夜夜澡人人爽人人喊a-99久久久无码国产精品9-国产亚洲日韩欧美综合