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染色体核型图多因素量化评分模型的构建

Construction of a Multi-Factor Quantitative Scoring Model for Chromosome Karyotype Analysis

  • 摘要:
    目的 设计多因素量化染色体核型图像质量评价模型用于辅助人工选图,提高选图的效率和染色体核型分析的正确率。
    方法 通过已有研究和临床专家意见选择染色体交叉度、长度、清晰度、分散度、弯曲度等5项指标作为构建图片质量评价模型的量化指标,设计相应的算法对其进行评分。以专家人工审核结果为金标准,建立染色体核型图片分析结果是否正确的数据集。通过单因素分析和多因素分析判断各量化指标在核型识别正确和错误之间是否有差异,确定图片质量评价指标,并构建选图质量指数,建立核型分析结果预测模型。
    结果 共对2708例患者的13540张染色体图片进行了人工分析,经专家组审核,其中416张存在核型识别错误。对每个图片质量候选指标设定测量算法并计算得分,经过单因素和多因素分析,染色体弯曲度、交叉度、清晰度及长度评分均能影响染色体核型识别准确性,而分散度评分在识别正确组和错误组之间差异并无统计意义(P=0.133);根据所得的影响因素构建图片质量指数,经过检验,质量指数每增加1分,分析结果出错的风险就能降低8.4%。随着质量指数分数的升高,错误率呈现下降趋势,质量指数为75分以下的图片错误率为3.88%,75分以上图片的错误率为1.95%。基于质量指数建立染色体核型结果是否正确的预测模型,AUC = 0.72(95%CI:0.67~0.77,P < 0.001),展示良好的预测效果。
    结论 图片质量指数和染色体核型评价结果预测模型能够更加有效地辅助人工选图。

     

    Abstract:
    Objective To design a multi-factor quantitative evaluation model for chromosomal karyotype image quality to assist manual image selection, thereby improving the efficiency of image selection and the accuracy of karyotype analysis.
    Methods Based on existing literature and clinical expert opinion, five indicators—chromosomal crossover degree, length, clarity, dispersion, and curvature—were selected as quantitative measures for constructing the image quality evaluation model, and corresponding algorithms were designed to score each indicator. Using expert manual review results as the gold standard, a dataset comprising chromosomal karyotype images labeled with whether the analytical results were correct was established. Univariate and multivariate analyses were performed to determine whether significant differences existed in each quantitative indicator between karyotypically correct and incorrect images. Indicators demonstrating significant associations were retained to construct a selection quality index and to establish a predictive model for karyotype analysis outcomes.
    Results A total of 13 540 chromosomal images from 2708 patients underwent manual analysis, of which 416 images were identified by the expert panel as containing karyotype recognition errors. Measurement algorithms were developed and scores were calculated for each candidate image quality indicator. Univariate and multivariate analyses revealed that the scores for chromosomal curvature, crossover degree, clarity, and length significantly influenced the accuracy of karyotype recognition, whereas no statistically significant difference in dispersion score was observed between the correct and incorrect recognition groups (P = 0.133). Based on the identified contributing factors, a composite image quality index was constructed. Validation demonstrated that for every 1-point increase in the quality index, the risk of analytical error decreased by 8.4%. A declining trend in error rates was observed with increasing quality index scores; the error rate among images with a quality index below 75 was 3.88%, compared with 1.95% among images scoring 75 or above. A predictive model for the correctness of karyotype analysis outcomes, established based on the quality index, demonstrated favorable predictive performance with an area under the ROC curve (AUC) of 0.72 (95% CI: 0.67-0.77, P < 0.001).
    Conclusion The image quality index and the predictive model for karyotype evaluation outcomes can effectively assist manual image selection in chromosomal karyotype analysis.

     

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