• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

同型纯合镰状细胞病伴慢性腿部溃疡患者的血液黏度和炎症及黏附标志物的表达。

Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers.

机构信息

Department of Basic Medical Sciences, Physiology Section, University of the West Indies, Mona, Kingston 7, Jamaica.

出版信息

PLoS One. 2013 Jul 26;8(7):e68929. doi: 10.1371/journal.pone.0068929. Print 2013.

DOI:10.1371/journal.pone.0068929
PMID:23922670
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3724890/
Abstract

OBJECTIVE

To determine differences in TNF-α, IL-1β, IL-10, sICAM-1 concentrations, leg hypoxia and whole blood viscosity (WBV) at shear rates of 46 sec(-1) and 230 sec(-1) in persons with homozygous S sickle cell disease (SCD) with and without chronic leg ulceration and in AA genotype controls.

DESIGN

&

METHODS

fifty-five age-matched participants were recruited into the study: 31 SS subjects without leg ulcers (SSn), 24 SS subjects with leg ulcers (SSu) and 18 AA controls. Haematological indices were measured using an AC.Tron Coulter Counter. Quantification of inflammatory, anti-inflammatory and adhesion molecules was performed by ELISA. Measurement of whole blood viscosity was done using a Wells Brookfield cone-plate viscometer. Quantification of microvascular tissue oxygenation was done by Visible Lightguide spectrophotometry.

RESULTS

TNF-α and whole blood viscosity at 46 sec(-1) and 230 sec(-1) (1.75, 2.02 vs. 0.83, 1.26, p<0.05) were significantly greater in sickle cell disease subjects than in controls. There were no differences in plasma concentration of sICAM-1, IL-1β and IL-10 between SCD subjects and controls. IL-1β (median, IQR: 0.96, 1.7 vs. 0, 0.87; p<0.01) and sICAM-1 (226.5, 156.48 vs. 107.63, 121.5, p<0.005) were significantly greater in SSu group compared with SSn. However there were no differences in TNF-α (2, 3.98 vs. 0, 2.66) and IL-10 (13.34, 5.95 vs. 11.92, 2.99) concentrations between SSu and SSn. WBV in the SSu group at 46 sec(-1) and at 230 Sec 1 were 1.9 (95%CI; 1.2, 3.1) and 2.3 (1.2, 4.4) times greater than in the SSn group. There were no differences in the degree of tissue hypoxia as determined by lightguide spectrophotometry.

CONCLUSION

Inflammatory, adhesion markers and WBV may be associated with leg ulceration in sickle cell disease by way of inflammation-mediated vasoocclusion/vasoconstriction. Impaired skin oxygenation does not appear to be associated with chronic ulcers in these subjects with sickle cell disease.

摘要

目的

确定 TNF-α、IL-1β、IL-10、sICAM-1 浓度、腿部缺氧和全血粘度(WBV)在剪切率为 46 秒(-1)和 230 秒(-1)时,在纯合子 S 镰状细胞病(SCD)患者中有无慢性腿部溃疡以及 AA 基因型对照组中的差异。

设计和方法

招募了 55 名年龄匹配的参与者进行研究:31 名无腿部溃疡的 SS 受试者(SSn),24 名有腿部溃疡的 SS 受试者(SSu)和 18 名 AA 对照组。使用 AC.Tron Coulter 计数器测量血液学指标。通过 ELISA 定量测定炎症、抗炎和粘附分子。使用 Wells Brookfield 锥板粘度计测量全血粘度。使用可见光导分光光度法定量测量微血管组织氧合。

结果

与对照组相比,镰状细胞病患者的 TNF-α 和 46 秒(-1)和 230 秒(-1)时的全血粘度(1.75、2.02 与 0.83、1.26,p<0.05)显著更高。SCD 患者与对照组之间血浆 sICAM-1、IL-1β 和 IL-10 浓度无差异。与 SSn 组相比,IL-1β(中位数,IQR:0.96、1.7 与 0、0.87;p<0.01)和 sICAM-1(226.5、156.48 与 107.63、121.5,p<0.005)明显更高。然而,SSu 组与 SSn 组之间 TNF-α(2、3.98 与 0、2.66)和 IL-10(13.34、5.95 与 11.92、2.99)浓度无差异。SSu 组在 46 秒(-1)和 230 秒(-1)时的 WBV 分别为 1.9(95%CI;1.2、3.1)和 2.3(1.2、4.4)倍高于 SSn 组。通过导光分光光度法确定的组织缺氧程度没有差异。

结论

炎症、粘附标志物和 WBV 可能通过炎症介导的血管阻塞/血管收缩与镰状细胞病的腿部溃疡有关。在这些镰状细胞病患者中,皮肤氧合受损似乎与慢性溃疡无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/43fd51961c42/pone.0068929.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/c80c1019ab91/pone.0068929.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/fa4ce00667a3/pone.0068929.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/3c4c1dd9b1c1/pone.0068929.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/2756dd19ac4d/pone.0068929.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/43fd51961c42/pone.0068929.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/c80c1019ab91/pone.0068929.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/fa4ce00667a3/pone.0068929.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/3c4c1dd9b1c1/pone.0068929.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/2756dd19ac4d/pone.0068929.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c99/3724890/43fd51961c42/pone.0068929.g005.jpg

相似文献

1
Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers.同型纯合镰状细胞病伴慢性腿部溃疡患者的血液黏度和炎症及黏附标志物的表达。
PLoS One. 2013 Jul 26;8(7):e68929. doi: 10.1371/journal.pone.0068929. Print 2013.
2
Optimal haematocrit in subjects with normal haemoglobin genotype (HbAA), sickle cell trait (HbAS), and homozygous sickle cell disease (HbSS).血红蛋白基因型正常(HbAA)、镰状细胞特征(HbAS)和纯合镰状细胞病(HbSS)患者的最佳血细胞比容。
Clin Hemorheol Microcirc. 2011;47(4):253-60. doi: 10.3233/CH-2011-1387.
3
Oxygen delivery index in subjects with normal haemoglobin (HbAA), sickle cell trait (HbAS) and homozygous sickle cell disease (HbSS).具有正常血红蛋白(HbAA)、镰状细胞性状(HbAS)和纯合子镰状细胞病(HbSS)的受试者的氧输送指数。
Clin Hemorheol Microcirc. 2008;40(4):303-9.
4
Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers.纯合子镰状细胞(SS)病和慢性腿部溃疡患者的静脉功能异常。
Clin Sci (Lond). 2000 Jun;98(6):667-72.
5
Decreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcers.镰状细胞贫血和复发性腿部溃疡患者的血细胞比容与粘度比值降低,乳酸脱氢酶水平升高。
PLoS One. 2013 Nov 4;8(11):e79680. doi: 10.1371/journal.pone.0079680. eCollection 2013.
6
Oxygen delivery index in homozygous sickle cell disease: steady and crisis states.纯合子镰状细胞病中的氧输送指数:稳定状态和危象状态
Br J Biomed Sci. 2009;66(3):148-9. doi: 10.1080/09674845.2009.11730262.
7
Evaluation of Th17 related cytokines associated with clinical and laboratorial parameters in sickle cell anemia patients with leg ulcers.镰状细胞贫血合并腿部溃疡患者中与临床和实验室参数相关的Th17相关细胞因子的评估。
Cytokine. 2014 Feb;65(2):143-7. doi: 10.1016/j.cyto.2013.11.012. Epub 2013 Dec 25.
8
Haematological factors associated with leg ulcer in sickle cell disease.镰状细胞病中与腿部溃疡相关的血液学因素。
Trop Geogr Med. 1987 Oct;39(4):354-6.
9
Red blood cell deformability is reduced in homozygous sickle cell disease patients with leg ulcers.患有腿部溃疡的纯合子镰状细胞病患者的红细胞变形性降低。
Clin Hemorheol Microcirc. 2016 Nov 25;64(2):199-204. doi: 10.3233/CH-162063.
10
High prevalence of pulmonary hypertension in homozygous sickle cell patients with leg ulceration.腿部溃疡的纯合子镰状细胞病患者中肺动脉高压的高患病率。
Clin Exp Hypertens. 2009 Feb;31(1):44-8. doi: 10.1080/10641960802404078.

引用本文的文献

1
Sticking together: Polymerization of sickle hemoglobin drives the multiscale pathophysiology of sickle cell disease.凝聚在一起:镰状血红蛋白的聚合驱动镰状细胞病的多尺度病理生理学。
Biophys Rev (Melville). 2025 Mar 20;6(1):011309. doi: 10.1063/5.0238698. eCollection 2025 Mar.
2
Plasma oxylipins in children with sickle cell disease: Associations with biomarkers of inflammation and endothelial activation.镰状细胞病患儿的血浆氧化脂质:与炎症和内皮激活生物标志物的关联
Prostaglandins Leukot Essent Fatty Acids. 2025 Jul;205:102670. doi: 10.1016/j.plefa.2025.102670. Epub 2025 Feb 24.
3
A Compact Differential Dynamic Microscopy-based Device (cDDM): An Approach Tool for Early Detection of Hypercoagulable State in Transfusion-Dependent-β-Thalassemia Patients.

本文引用的文献

1
Significant J-shaped association between body mass index (BMI) and diabetic foot ulcers.体质指数(BMI)与糖尿病足溃疡之间存在显著的 J 型关联。
Diabetes Metab Res Rev. 2011 May;27(4):402-9. doi: 10.1002/dmrr.1193.
2
Tumor necrosis factor receptor-associated periodic syndrome P46L and bilateral amputation in diabetes.肿瘤坏死因子受体相关周期性综合征P46L与糖尿病患者双侧截肢
Rheumatology (Oxford). 2010 Dec;49(12):2454-5. doi: 10.1093/rheumatology/keq227. Epub 2010 Jul 15.
3
Pattern of serum cytokine expression and T-cell subsets in sickle cell disease patients in vaso-occlusive crisis.
一种紧凑型差分动态显微镜设备(cDDM):用于早期检测输血依赖型β-地中海贫血患者高凝状态的方法工具。
ACS Appl Bio Mater. 2024 Jul 15;7(7):4710-4724. doi: 10.1021/acsabm.4c00516. Epub 2024 Jun 26.
4
Homozygote drepanocytosis: Ferric status and inflammation in world and Africa: Review article and meta analysis.纯合子镰状细胞贫血症:全球及非洲地区的铁状态与炎症:综述文章及荟萃分析
Health Sci Rep. 2023 Oct 4;6(10):e1609. doi: 10.1002/hsr2.1609. eCollection 2023 Oct.
5
Effects of Doxycycline Treatment on Hematological Parameters, Viscosity, and Cytokines in Canine Monocytic Ehrlichiosis.强力霉素治疗对犬单核细胞埃立克体病血液学参数、粘度和细胞因子的影响。
Biology (Basel). 2023 Aug 16;12(8):1137. doi: 10.3390/biology12081137.
6
The Rheology of the Carotid Sinus: A Path Toward Bioinspired Intervention.颈动脉窦的流变学:一条通向生物启发式干预的途径。
Front Bioeng Biotechnol. 2021 Jun 10;9:678048. doi: 10.3389/fbioe.2021.678048. eCollection 2021.
7
Treatment of recalcitrant chronic leg ulcer in a known sickle cell anaemia patient using honey and fresh hbaa red cell concentrate in a Nigerian secondary healthcare facility.在尼日利亚二级医疗机构中,使用蜂蜜和新鲜 HBAa 红细胞浓缩液治疗已知镰状细胞贫血患者的难治性慢性腿部溃疡。
Ann Afr Med. 2020 Oct-Dec;19(4):278-281. doi: 10.4103/aam.aam_53_19.
8
Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.全血黏度和红细胞黏附:镰状细胞病靶向和治愈疗法的潜在生物标志物。
Am J Hematol. 2020 Nov;95(11):1246-1256. doi: 10.1002/ajh.25933. Epub 2020 Aug 10.
9
Hemorheological Alterations and Oxidative Damage in Sickle Cell Anemia.镰状细胞贫血中的血液流变学改变与氧化损伤
Front Mol Biosci. 2019 Dec 4;6:142. doi: 10.3389/fmolb.2019.00142. eCollection 2019.
10
Role of some members of chemokine/cytokine network in the pathogenesis of thalassemia and sickle cell hemoglobinopathies: a mini review.趋化因子/细胞因子网络的某些成员在地中海贫血和镰状细胞血红蛋白病发病机制中的作用:一篇综述
Exp Hematol Oncol. 2019 Sep 11;8:21. doi: 10.1186/s40164-019-0145-x. eCollection 2019.
血管闭塞性危象期镰状细胞病患者血清细胞因子表达模式及T细胞亚群分析
Clin Vaccine Immunol. 2010 Apr;17(4):602-8. doi: 10.1128/CVI.00145-09. Epub 2010 Feb 3.
4
Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease.镰状细胞病成年患者的心肺并发症导致过早死亡。
Am J Hematol. 2010 Jan;85(1):36-40. doi: 10.1002/ajh.21569.
5
Oxygen delivery index in homozygous sickle cell disease: steady and crisis states.纯合子镰状细胞病中的氧输送指数:稳定状态和危象状态
Br J Biomed Sci. 2009;66(3):148-9. doi: 10.1080/09674845.2009.11730262.
6
Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.在纯合子镰状细胞贫血和镰状-血红蛋白C病中,红细胞聚集、聚集强度及血液的氧运输潜力均异常。
Haematologica. 2009 Aug;94(8):1060-5. doi: 10.3324/haematol.2008.005371.
7
New guidelines for hemorheological laboratory techniques.血液流变学实验室技术新指南。
Clin Hemorheol Microcirc. 2009;42(2):75-97. doi: 10.3233/CH-2009-1202.
8
Oxygen delivery index in subjects with normal haemoglobin (HbAA), sickle cell trait (HbAS) and homozygous sickle cell disease (HbSS).具有正常血红蛋白(HbAA)、镰状细胞性状(HbAS)和纯合子镰状细胞病(HbSS)的受试者的氧输送指数。
Clin Hemorheol Microcirc. 2008;40(4):303-9.
9
Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia.牙买加的静脉功能不全、贫困和乳酸脱氢酶是镰状细胞贫血患者腿部溃疡的重要预测因素。
Br J Haematol. 2008 Jul;142(1):119-25. doi: 10.1111/j.1365-2141.2008.07115.x. Epub 2008 May 8.
10
Assessment of oxygenation and perfusion in the tongue and oral mucosa by visible spectrophotometry and laser Doppler flowmetry in healthy subjects.通过可见分光光度法和激光多普勒血流仪对健康受试者舌部和口腔黏膜的氧合和灌注进行评估。
Adv Exp Med Biol. 2008;614:227-33. doi: 10.1007/978-0-387-74911-2_26.