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非侵入性 2 型糖尿病筛查:亚洲裔印度人群中 SCOUT DS 的临床评估。

Noninvasive type 2 diabetes screening: clinical evaluation of SCOUT DS in an Asian Indian cohort.

机构信息

Madras Diabetes Research Foundation & Dr. Mohan's Diabetes Specialities Centre, Gopalapuram, WHO Collaborating Centre for Non-Communicable Diseases Prevention and Control, IDF Centre for Education, Chennai, India.

出版信息

Diabetes Technol Ther. 2013 Jan;15(1):39-45. doi: 10.1089/dia.2012.0204. Epub 2012 Nov 14.

DOI:10.1089/dia.2012.0204
PMID:23150995
Abstract

OBJECTIVE

This study evaluated the noninvasive, point-of-care diabetes screening device, Scout DS (VeraLight Inc., Albuquerque, NM) (SCOUT), in a native Asian Indian cohort.

RESEARCH DESIGN AND METHODS

SCOUT is a tabletop, skin fluorescence spectrometer that reports a risk score following a 3-4-min noninvasive measurement of a subject's left volar forearm. SCOUT, fasting plasma glucose (FPG), and hemoglobin A(1c) (A1C) were compared for detection of abnormal glucose tolerance (AGT) in a cohort of 256 subjects without previous diagnosis of diabetes or impaired glucose tolerance in Chennai, India. After an overnight fast, a 75-g, 2-h oral glucose tolerance test was administered, and AGT was defined as a plasma glucose value ≥ 140 mg/dL (7.8 mmol/dL). Sensitivity, false-positive rate (FPR), and receiver-operating characteristics area under the curve for AGT detection were computed for SCOUT, FPG, and A1C. Intra-day reproducibility of SCOUT was assessed.

RESULTS

SCOUT, FPG, and A1C (at respective thresholds of 50, 110 mg/dL, and 5.7%) exhibited sensitivities of 87%, 32%, and 86%, respectively, and FPR of 52%, 3%, and 58%, respectively. For the 177 subjects receiving a valid SCOUT Diabetes Score on both measurement attempts, the coefficient of variation was 5.8%, and the Pearson correlation was 0.91. A SCOUT score could be obtained on 91% of subjects after two attempts.

CONCLUSIONS

The performance of SCOUT is similar to that of A1C, whereas FPG had a much lower sensitivity. SCOUT is an effective tool for AGT screening in Asian Indians.

摘要

目的

本研究评估了非侵入性、即时检测的糖尿病筛查设备 Scout DS(VeraLight Inc.,新墨西哥州阿尔伯克基)(SCOUT)在亚洲本地印度人群中的表现。

研究设计和方法

SCOUT 是一种台式、皮肤荧光光谱仪,在对受试者左掌心进行 3-4 分钟的无创测量后,报告风险评分。在印度钦奈的 256 名受试者中,无糖尿病或糖耐量受损既往诊断史,比较 SCOUT、空腹血糖(FPG)和血红蛋白 A1c(A1C)对异常葡萄糖耐量(AGT)的检测能力。受试者隔夜禁食后,给予 75g、2 小时口服葡萄糖耐量试验,将血浆葡萄糖值≥140mg/dL(7.8mmol/dL)定义为 AGT。计算 SCOUT、FPG 和 A1C 检测 AGT 的敏感性、假阳性率(FPR)和受试者工作特征曲线下面积。评估 SCOUT 的日内重复性。

结果

SCOUT、FPG 和 A1C(各自的阈值分别为 50、110mg/dL 和 5.7%)的敏感性分别为 87%、32%和 86%,FPR 分别为 52%、3%和 58%。在 177 名接受两次测量均有效 SCOUT 糖尿病评分的受试者中,变异系数为 5.8%,Pearson 相关系数为 0.91。两次尝试后,可获得 91%受试者的 SCOUT 评分。

结论

SCOUT 的性能与 A1C 相似,而 FPG 的敏感性要低得多。SCOUT 是亚洲印度人进行 AGT 筛查的有效工具。

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