R. Meenakshisundaram, P. Thirumalaikolundusubramanian
{"title":"Biomarkers And Screening Tests For Abdominal Aortic Aneurysm: A Brief Review","authors":"R. Meenakshisundaram, P. Thirumalaikolundusubramanian","doi":"10.5580/1913","DOIUrl":null,"url":null,"abstract":"Background: Abdominal aortic aneurysm (AAA), though it is a deadly disease, it remains silent invariably. Hence, one has to suspect and evaluate AAA at least in a susceptible group at an earlier stage to reduce the morbidity and mortality. Objective: To find out the usefulness and limitations of various biomarkers in diagnosing AAA and drug to prevent/treat it. Material And Methods: Published data were collected from web using keywords biomarkers, clinical methods, screening tests and abdominal aortic aneurysm. Results: Biomarkers identified for AAA are osteopontin (OPN), osetoprotegrin (OPG), Matrix metalloproteinase-9 (MMP-9), circulating levels of tumor necrosis factor-α, interleukin-1β, interleukin -6, interferon-γ, amino terminal propeptide of type 3 collagen, C-reactive protein (CRP), fibrinogen, total WBC count, albumin and ultrasonogram of abdomen. Co-existing illnesses influence inflammatory biomarkers. The promising biomarker is Osteopontin and this is useful to assess the status and progression of AAA. The drug, Irbesartan (angiotensin II blocker) has been shown to reduce the size of aneurysm by dwindling the secretion of osteoprotegrin. Conclusions: Primary focus should be on early detection and management. To achieve this goal, orientation of primary health care professionals towards symptoms and signs of AAA, surgeons to look for the same during abdominal surgeries and radiologists to search for it during USG/ CT scan of abdomen. *This paper was presented in the conference “SUMMIT ON ACUTE AORTIC DISEASES: LUX ET VERITAS” held at Yale University Medical School, New Haven, Connecticut, USA on November 1-2, 2007. This program was conducted by Promedica International CME, a California corporation.","PeriodicalId":330833,"journal":{"name":"The Internet Journal of Thoracic and Cardiovascular Surgery","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2008-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet Journal of Thoracic and Cardiovascular Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/1913","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Background: Abdominal aortic aneurysm (AAA), though it is a deadly disease, it remains silent invariably. Hence, one has to suspect and evaluate AAA at least in a susceptible group at an earlier stage to reduce the morbidity and mortality. Objective: To find out the usefulness and limitations of various biomarkers in diagnosing AAA and drug to prevent/treat it. Material And Methods: Published data were collected from web using keywords biomarkers, clinical methods, screening tests and abdominal aortic aneurysm. Results: Biomarkers identified for AAA are osteopontin (OPN), osetoprotegrin (OPG), Matrix metalloproteinase-9 (MMP-9), circulating levels of tumor necrosis factor-α, interleukin-1β, interleukin -6, interferon-γ, amino terminal propeptide of type 3 collagen, C-reactive protein (CRP), fibrinogen, total WBC count, albumin and ultrasonogram of abdomen. Co-existing illnesses influence inflammatory biomarkers. The promising biomarker is Osteopontin and this is useful to assess the status and progression of AAA. The drug, Irbesartan (angiotensin II blocker) has been shown to reduce the size of aneurysm by dwindling the secretion of osteoprotegrin. Conclusions: Primary focus should be on early detection and management. To achieve this goal, orientation of primary health care professionals towards symptoms and signs of AAA, surgeons to look for the same during abdominal surgeries and radiologists to search for it during USG/ CT scan of abdomen. *This paper was presented in the conference “SUMMIT ON ACUTE AORTIC DISEASES: LUX ET VERITAS” held at Yale University Medical School, New Haven, Connecticut, USA on November 1-2, 2007. This program was conducted by Promedica International CME, a California corporation.
背景:腹主动脉瘤(AAA)是一种致命的疾病,但它总是沉默不语。因此,至少在易感人群中,必须在早期阶段怀疑和评估AAA,以降低发病率和死亡率。目的:探讨各种生物标志物在AAA诊断及预防/治疗方面的应用价值和局限性。材料和方法:使用关键词生物标志物、临床方法、筛选试验和腹主动脉瘤从网上收集已发表的数据。结果:AAA的生物标志物有骨桥蛋白(OPN)、骨蛋白素(OPG)、基质金属蛋白酶-9 (MMP-9)、循环肿瘤坏死因子-α、白细胞介素-1β、白细胞介素-6、干扰素-γ、3型胶原氨基端前肽、c反应蛋白(CRP)、纤维蛋白原、总白细胞计数、白蛋白和腹部超声图。共存的疾病影响炎症生物标志物。最有希望的生物标志物是骨桥蛋白,它有助于评估AAA的状态和进展。厄贝沙坦(血管紧张素II阻滞剂)已被证明可以通过减少骨蛋白素的分泌来缩小动脉瘤的大小。结论:应重视早期发现和早期管理。为了实现这一目标,初级卫生保健专业人员应关注AAA的症状和体征,外科医生应在腹部手术中寻找相同的症状,放射科医生应在腹部USG/ CT扫描中寻找相同的症状。*本文发表于2007年11月1-2日在美国康涅狄格州纽黑文耶鲁大学医学院举行的“急性主动脉疾病峰会:LUX ET VERITAS”会议上。这个项目是由加州公司Promedica International CME实施的。