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贝塞斯达标准用于微卫星不稳定性检测:对林奇综合征新病例检测的影响。

Bethesda criteria for microsatellite instability testing: impact on the detection of new cases of Lynch syndrome.

机构信息

Serviço de Gastrenterologia, Instituto Português de Oncologia de Lisboa Francisco Gentil, E.P.E., Rua Professor Lima Basto 1099-023, Lisbon, Portugal.

出版信息

Fam Cancer. 2012 Dec;11(4):571-8. doi: 10.1007/s10689-012-9550-6.

Abstract

In 1997 Bethesda Guidelines (BG) were established and in 2004 those criteria were revised (RBG), with the main goal of selecting colorectal cancers (CRC) that should be subjected to microsatellite instability (MSI) testing. High microsatellite instability (MSI-H) is an intermediate marker for mutational analysis of the mismatch repair (MMR) genes involved in the genesis of Lynch Syndrome (LS). We aimed to evaluate and compare BG/RBG in the detection of MSI-H and subsequent identification of pathogenic MMR genes mutations. We included 174 patients with CRC and indication for MSI analysis according to BG or RBG. MSI testing was performed with the Bethesda markers and mutational analysis of MLH1, MSH2 and MSH6 genes undertaken with DGGE, MLPA and direct sequencing. One hundred fourteen of 174 patients (65.5 %) fulfilled BG and all of them RBG. With the BG, MSI-H was detected in 37/114 (32.5 %) CRCs and mutational analysis was positive in 14/37 (37.8 %) patients. The RBG led to detection of MSI-H in 49/174 (28.2 %) of the CRCs, having the mutational analysis been positive in 16/49 (32.7 %) patients. We could identify 14/114 (12.3 %) new cases of LS, through BG and 16/174 (9.2 %) via RBG. BG presented a similar overall percentage for the detection of MSI-H and mutations when compared with RBG. RBG implicated the analysis of more patients, though they gave rise to detection of two additional LS cases. This difference has a significant impact on the establishment of preventive measures, mainly for CRC, in all the mutation-carriers belonging to these families.

摘要

1997 年制定了贝塞斯达指南(BG),2004 年对这些标准进行了修订(RBG),主要目的是选择应进行微卫星不稳定性(MSI)检测的结直肠癌(CRC)。高度微卫星不稳定性(MSI-H)是错配修复(MMR)基因突变分析的中间标志物,参与林奇综合征(LS)的发生。我们旨在评估和比较 BG/RBG 在检测 MSI-H 以及随后识别致病性 MMR 基因突变方面的作用。我们纳入了 174 名符合 BG 或 RBG 进行 MSI 分析适应证的 CRC 患者。采用贝塞斯达标志物进行 MSI 检测,采用 DGGE、MLPA 和直接测序对 MLH1、MSH2 和 MSH6 基因进行突变分析。174 名患者中有 114 名(65.5%)符合 BG 标准,均符合 RBG 标准。根据 BG,37/114(32.5%)例 CRC 检测到 MSI-H,14/37(37.8%)例患者的突变分析为阳性。RBG 导致 174 例 CRC 中有 49/174(28.2%)例检测到 MSI-H,16/49(32.7%)例患者的突变分析为阳性。通过 BG 可识别 14/114(12.3%)例新的 LS 病例,通过 RBG 可识别 16/174(9.2%)例。BG 和 RBG 检测 MSI-H 和突变的总体百分比相似。RBG 涉及更多的患者分析,尽管它们又发现了 2 例额外的 LS 病例。这种差异对所有突变携带者家族的 CRC 等预防性措施的建立具有重要影响。

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