张培, 周华, 杨敏. 缩孔综合征的研究进展[J]. 临床肾脏病杂志, 2022, 22(3): 238-242. DOI: 10.3969/j.issn.1671-2390.2022.03.011
    引用本文: 张培, 周华, 杨敏. 缩孔综合征的研究进展[J]. 临床肾脏病杂志, 2022, 22(3): 238-242. DOI: 10.3969/j.issn.1671-2390.2022.03.011
    Zhang Pei, Zhuo Hua, Yang Min. Research advances of shrunken pore syndrome[J]. Journal of Clinical Nephrology, 2022, 22(3): 238-242. DOI: 10.3969/j.issn.1671-2390.2022.03.011
    Citation: Zhang Pei, Zhuo Hua, Yang Min. Research advances of shrunken pore syndrome[J]. Journal of Clinical Nephrology, 2022, 22(3): 238-242. DOI: 10.3969/j.issn.1671-2390.2022.03.011

    缩孔综合征的研究进展

    Research advances of shrunken pore syndrome

    • 摘要: 缩孔综合征(shrunken pore syndrome,SPS)是指在排除肾外因素影响血浆胱抑素C与肌酐的前提下,基于血浆胱抑素C估算的肾小球滤过率(eGFRcystatin C)显著低于基于肌酐估算的肾小球滤过率(eGFRcreatinine)的一种病理生理状态。研究表明,SPS患者预后不良,SPS患者心血管疾病发病率和病死率很高。目前研究认为,SPS的机制可能与肾小球滤过膜孔径缩小相关,使得肾脏对相对分子质量为5~30 000的分子滤过减少,并以此提出治疗方案的猜想。我们对SPS的病理生理机制、诊断、临床结局和治疗方法的研究进展进行综述,旨在提高人们对SPS的临床认识,加强对SPS的早期识别能力。

       

      Abstract: As a pathophysiologic state in the absence of extrarenal influences on cystatin C or creatinine concentration,shrunken pore syndrome (SPS) occurs when estimated glomerular filtration rate (eGFR) based upon plasma cystatin C becomes significantly lower than its counterpart based upon creatinine.Studies have demonstrated that SPS patients have a poor prognosis and carry a high risk for cardiovascular morbidity and mortality.A potential mechanism of SPS is associated with a reduction of pore size of glomerular filtration membrane and a lower glomerular filtration of molecules 5~30,000.Corresponding treatment is thus proposed based upon the conjecture.This review summarized the latest researches in pathophysiological mechanism,diagnosis&treatment and clinical outcomes of SPS.It was intended to enhance its clinical awareness and boost the capability of its early identification.

       

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