Center for International Health Research, Rhode Island Hospital and Alpert Medical School of Brown University, Providence, Rhode Island.
Department of Transfusion Medicine, Rhode Island Hospital and the Miriam Hospitals, Providence, Rhode Island.
Int J Lab Hematol. 2018 Dec;40(6):655-662. doi: 10.1111/ijlh.12900. Epub 2018 Jul 13.
South-East Asian ovalocytosis (SAO) is a common inherited red blood cell polymorphism in South-East Asian and Melanesian populations, coinciding with areas of malaria endemicity. Validation of light microscopy as a diagnostic alternative to molecular genotyping may allow for its cost-effective use either prospectively or retrospectively by analysis of archived blood smears.
We assessed light microscopic diagnosis of SAO compared to standard PCR genotyping. Three trained microscopists each assessed the same 971 Giemsa-stained thin blood films for which SAO genotypic confirmation was available by PCR. Generalized mixed modeling was used to estimate the sensitivity, specificity, positive predictive value, and negative predictive value of light microscopy vs "gold standard" PCR.
Among red cell morphologic parameters evaluated, knizocytes, rather than ovalocytic morphology, proved the strongest predictor of SAO status (odds ratio [OR] = 19.2; 95% confidence interval [95% CI] = 14.6-25.3; P ≤ 0.0001). The diagnostic performance of a knizocyte-centric microscopic approach was microscopist dependent: two microscopists applied this approach with a sensitivity of 0.89 and a specificity of 0.93. Inter-rater reliability among the microscopists (κ = 0.20) as well as between gold standard and microscopist (κ = 0.36) underperformed due to misclassification of stomatocytes as knizocytes by one microscopist, but improved substantially when excluding the error-prone reader (κ = 0.65 and 0.74, respectively).
Light microscopic diagnosis of SAO by knizocyte visual cue performed comparable to time-consuming and costlier molecular methods, but requires specific training that includes successful differentiation of knizocytes from stomatocytes.
东南亚卵形红细胞增多症(SAO)是东南亚和美拉尼西亚人群中常见的遗传性红细胞多态性,与疟疾流行地区相吻合。通过对存档血涂片进行分析,验证光镜检查作为分子基因分型的替代诊断方法具有成本效益,无论是前瞻性还是回顾性都可以使用。
我们评估了光镜检查诊断 SAO 的效果,并与标准 PCR 基因分型进行了比较。三名经过培训的显微镜检查师分别评估了 971 张吉姆萨染色的薄血片,这些血片的 SAO 基因型通过 PCR 得到确认。广义混合模型用于估计光镜检查与“金标准”PCR 相比的敏感性、特异性、阳性预测值和阴性预测值。
在所评估的红细胞形态学参数中,皱缩红细胞而不是卵形红细胞形态,是 SAO 状态的最强预测因子(优势比 [OR] = 19.2;95%置信区间 [95%CI] = 14.6-25.3;P ≤ 0.0001)。以皱缩红细胞为中心的微观方法的诊断性能依赖于显微镜检查师:两名显微镜检查师应用该方法的敏感性为 0.89,特异性为 0.93。显微镜检查师之间的观察者间可靠性(κ = 0.20)以及金标准和显微镜检查师之间的可靠性(κ = 0.36)较差,原因是一名显微镜检查师将口形红细胞错误地归类为皱缩红细胞,但当排除易出错的读者时,可靠性大大提高(κ 分别为 0.65 和 0.74)。
通过皱缩红细胞的视觉提示进行光镜检查诊断 SAO 的效果与耗时且昂贵的分子方法相当,但需要特定的培训,包括成功区分皱缩红细胞和口形红细胞。