Suppr超能文献

常染色体显性多囊肾病的当前诊断评估

Current diagnostic evaluation of autosomal dominant polycystic kidney disease.

作者信息

Wołyniec Wojciech, Jankowska Magdalena Maria, Król Ewa, Czarniak Piotr, Rutkowski Bolesław

机构信息

Department of Nephrology, Transplantology and Internal Medicine, Medical University, Gdańsk, Poland.

出版信息

Pol Arch Med Wewn. 2008 Dec;118(12):767-73.

Abstract

Despite changing epidemiology of chronic kidney disease, autosomal dominant polycystic kidney disease (ADPKD) is one of the most prevalent causes of end stage renal disease. The first symptoms of the disease occur usually in the 3rd or 4th decade of life, however, it can often be diagnosed much earlier. Advances in the understanding of the disease may lead, in the near future, to slowing the progression of ADPKD in asymptomatic individuals. ADPKD is diagnosed on the basis of family history (autosomal dominant inheritance) and radiological imaging. Ultrasound examination (US) of the kidneys is the most important imaging diagnostic method. US is highly sensitive and specific in patients >30 years of age. In US, Ravine criteria are applied and their modifications with other imaging techniques (computed tomography [CT], magnetic resonance [MR]). In all cases, however, there are multiple cysts in both kidneys and, importantly, concomitant renal enlargement can be observed, which is typical of ADPKD. High expectations for early ADPKD diagnosis are risen by genetics and proteomics. However, these methods are not used routinely. The most sensitive parameter in the evaluation of the disease progression is total renal volume. This parameter is presently used in clinical studies, but its utility in monitoring an individual patient has not been fully proven. Unfortunately, MR and CT are expensive and in case of significantly enlarged kidneys US does not yield accurate assessment of their size and is not sensitive enough for monitoring the disease progression. The rate of glomerular filtration rate (GFR) decline is usually constant. Therefore, it is important to monitor GFR in individuals who have developed renal insufficiency. Other tests, including markers of kidney injury, e.g. albuminuria, or vascular flow parameters, are used mainly in clinical studies. Thus, before more efficient therapeutic approaches have been developed, an early diagnosis and prevention of the disease complications are most essential.

摘要

尽管慢性肾脏病的流行病学情况不断变化,但常染色体显性多囊肾病(ADPKD)仍是终末期肾病最常见的病因之一。该病的首发症状通常出现在30或40多岁,但往往能在更早阶段被诊断出来。对该疾病认识的进展可能在不久的将来减缓无症状个体中ADPKD的进展。ADPKD根据家族史(常染色体显性遗传)和影像学检查进行诊断。肾脏超声检查(US)是最重要的影像学诊断方法。US对30岁以上患者具有高度敏感性和特异性。在US检查中,应用Ravine标准及其与其他成像技术(计算机断层扫描[CT]、磁共振成像[MR])的联合应用。然而,在所有病例中,双侧肾脏均有多个囊肿,重要的是,可以观察到肾脏同时增大,这是ADPKD的典型表现。遗传学和蛋白质组学提高了对ADPKD早期诊断的期望。然而,这些方法并未常规使用。评估疾病进展最敏感的参数是肾脏总体积。该参数目前用于临床研究,但其在监测个体患者方面的效用尚未得到充分证实。不幸的是,MR和CT费用昂贵,而且在肾脏明显增大的情况下,US无法准确评估其大小,对监测疾病进展也不够敏感。肾小球滤过率(GFR)下降速度通常较为恒定。因此,监测肾功能不全患者的GFR很重要。其他检查,包括肾脏损伤标志物,如蛋白尿,或血管血流参数,主要用于临床研究。因此,在开发出更有效的治疗方法之前,早期诊断和预防疾病并发症最为关键。

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