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首页> 外文期刊>The Journal of Nuclear Medicine >Kinetic studies with iodine-123-labeled serum amyloid P component in patients with systemic AA and AL amyloidosis and assessment of clinical value.
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Kinetic studies with iodine-123-labeled serum amyloid P component in patients with systemic AA and AL amyloidosis and assessment of clinical value.

机译:用碘123标记的系统性AA和AL淀粉样变性患者的血清淀粉样蛋白P成分的动力学研究以及临床价值评估。

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In systemic amyloidosis, widespread amyloid deposition interferes with organ function, frequently with fatal consequences. Diagnosis rests on demonstrating amyloid deposits in the tissues, traditionally with histology although scintigraphic imaging with radiolabeled serum amyloid P component (SAP) has lately been developed as a specific noninvasive alternative. We report a detailed analysis of the abnormal turnover of SAP in patients with systemic amyloidosis and an assessment of its clinical value. METHODS: Iodine-123-labeled human SAP (200 MBq) SAP was injected intravenously into 49 patients with histologically proven systemic AA- or AL- amyloidosis and in 7 control subjects. Plasma clearance and whole-body retention of labeled SAP were analyzed over 48 hr using plasma sampling, whole-body gamma camera imaging and measurement of radioactivity in the urine. The rate of SAP synthesis and interstitial exchange were determined, and the size of the amyloid compartment was compared with clinical estimates of whole-body amyloid load and patient survival. RESULTS: All plasma time-activity curves were biphasic. In comparison with control subjects, patients with amyloidosis showed significantly faster plasma disappearance [4-hr value: AA 48% +/- 18%, AL 45% +/- 15% versus 65% +/- 8% (p < 0.05)], higher total-body retention 48 hr p.i. [AA 74% +/- 14%, AL 73% +/- 17% versus 46% +/- 15% (p < 0.01)] and especially higher extravascular retention 48 hr p.i. [AA 59% +/- 16%, AL 58% +/- 19% versus 30% +/- 14% (p < 0.01)]. Extravascular retention correlated with clinical estimation of the amyloid load. If extravascular retention values in patients with AL amyloidosis were over 60%, survival was decreased (median 4 versus 23 mo, p < 0.001). Markedly increased interstitial exchange rates were present in amyloidosis (AA 64 +/- 61, AL 50 +/- 37 versus 18 +/- 8 mg/hr), whereas the SAP synthesis rate did not differ from the control values (AA 5.0 +/- 3.0, AL 5.5 +/- 3.2 versus 4.5 +/- 1.4 mg/hr). CONCLUSION: The presence of systemic amyloidosis is characterized by accelerated initial clearance of 123I-SAP from the plasma and increased interstitial exchange rate and extravascular retention. These findings reflect reversible binding of radiolabeled SAP to amyloid deposits and provide clinically useful information for diagnosis, monitoring of therapy and prognosis in patients with systemic amyloidosis.
机译:在系统性淀粉样变性病中,广泛的淀粉样蛋白沉积会干扰器官功能,并经常导致致命后果。诊断通常取决于组织学中淀粉样蛋白的沉积,传统上是用组织学方法进行的,尽管近来已开发了放射标记的血清淀粉样蛋白P组分(SAP)的闪烁显像作为一种特定的非侵入性替代方法。我们报告了系统性淀粉样变性患者SAP异常营业额的详细分析及其临床价值评估。方法:将碘-123标记的人SAP(200 MBq)SAP静脉注射到49例经组织学证实为系统性AA或AL-淀粉样变性的患者中,并在7名对照受试者中进行注射。使用血浆采样,全身伽马射线照相成像和尿液中放射性测量,在48小时内分析了标记SAP的血浆清除率和全身滞留率。确定SAP合成和间质交换的速率,并将淀粉样蛋白区室的大小与全身淀粉样蛋白负荷和患者存活率的临床估计值进行比较。结果:所有血浆时间-活动曲线均为双相的。与对照组相比,淀粉样变性患者的血浆消失明显更快[4小时值:AA 48%+/- 18%,AL 45%+/- 15%对65%+/- 8%(p <0.05) ],更高的全身滞留率48 hr pi [AA 74%+/- 14%,AL 73%+/- 17%与46%+/- 15%(p <0.01)],尤其是48 h p.i更高的血管外滞留性。 [AA 59%+/- 16%,AL 58%+/- 19%对30%+/- 14%(p <0.01)]。血管外滞留与淀粉样蛋白负荷的临床估计有关。如果AL淀粉样变性患者的血管外滞留值超过60%,则生存率降低(中位数4对23个月,p <0.001)。淀粉样变性中的间质交换速率显着增加(AA 64 +/- 61,AL 50 +/- 37与18 +/- 8 mg / hr),而SAP合成率与对照值无差异(AA 5.0 + +/- 3.0,AL 5.5 +/- 3.2与4.5 +/- 1.4 mg / hr)。结论:系统性淀粉样变性的存在的特征是加速了血浆中123I-SAP的初始清除,并增加了间质交换率和血管外滞留。这些发现反映了放射性标记的SAP与淀粉样蛋白沉积物的可逆结合,并为系统性淀粉样变性病患者的诊断,治疗监测和预后提供了临床有用的信息。

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