选择基于实验室的生物标志物,用于评估风险人群中维生素A缺乏症
Bryan M Gannon1,2, Samantha L Huey1,3, Neel H Mehta1
1Division of Nutritional Sciences, Cornell University, Ithaca, New York, USA.
The Cochrane database of systematic reviews
|May 28, 2025
概括
准确诊断维生素A缺乏症至关重要. 目前的诊断测试显示敏感度低 (0-54%),但特异性高 (74-94%),尽管由于研究的局限性,必须谨慎解释结果.
科学领域:
- 生物化学 生物化学
- 营养科学 营养科学
- 诊断准确性研究 诊断准确性研究
背景情况:
- 维生素A 缺乏带来了重大的全球健康风险,包括生长障碍,免疫力减弱,增加疾病易感性和死亡率.
- 可靠的诊断方法对于有效的临床治疗维生素A缺乏是必不可少的.
- 现有的诊断工具包括直接指数测量和剂量反应生物标志物.
研究的目的:
- 评估常用的亚临床维生素A缺乏指数测试的诊断准确性.
- 根据共变量来确定测试准确性的异质性潜在来源.
主要方法:
- 诊断准确性研究的系统审查和元分析.
- 在多个数据库 (CENTRAL,MEDLINE,Embase等) 进行了搜索. 在2022年8月之前.
- 包括使用参考标准和索引测试测量维生素A状态的研究;使用QUADAS-2评估偏差风险.
主要成果:
- 包括40项研究 (65项记录);没有一个被设计为诊断测试准确性研究.
- 与参考标准相比,血清/血视网醇 (SR) 的综合敏感性低 (10-54%),特异性中等至高 (79-94%).
- 视网醇结合蛋白 (RBP) 显示了低至中等的综合敏感性 (0-50%) 和高特异性 (76-98%). 相对剂量响应 (RDR) 显示了有限的可估计灵敏度,但具有高的特异性 (89-91%).
结论:
- 目前用于诊断维生素A缺乏症的方法通常具有低灵敏度和高特异性.
- 由于包含的研究的诊断测试准确性设计有限,研究结果应谨慎解释.
- 需要对母乳维生素A和修改RDR测试的准确性进行更多研究.
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