Norwich Medical School, University of East Anglia, Norwich, UK.
Department of Clinical Biochemistry, Norfolk and Norwich University Hospitals NHS Trust, Norwich, UK.
Diabet Med. 2019 Nov;36(11):1478-1486. doi: 10.1111/dme.14111. Epub 2019 Sep 3.
To investigate factors influencing diagnostic discordance for non-diabetic hyperglycaemia and Type 2 diabetes.
Some 10 000 adults at increased risk of diabetes were screened with HbA and fasting plasma glucose (FPG). The 2208 participants with initial HbA ≥ 42 mmol/mol (≥ 6.0%) or FPG ≥ 6.1 mmol/l were retested after a median 40 days. We compared the first and second HbA results, and consequent diagnoses of non-diabetic hyperglycaemia and Type 2 diabetes, and investigated predictors of discordant diagnoses.
Of 1463 participants with non-diabetic hyperglycaemia and 394 with Type 2 diabetes on first testing, 28.4% and 21.1% respectively had discordant diagnoses on repeated testing. Initial diagnosis of non-diabetic hyperglycaemia and/or impaired fasting glucose according to both HbA and FPG criteria, or to FPG only, made reclassification as Type 2 diabetes more likely than initial classification according to HbA alone. Initial diagnosis of Type 2 diabetes according to both HbA and FPG criteria made reclassification much less likely than initial classification according to HbA alone. Age, and anthropometric and biological measurements independently but inconsistently predicted discordant diagnoses and changes in HbA .
Diagnosis of non-diabetic hyperglycaemia or Type 2 diabetes with a single measurement of HbA in a screening programme for entry to diabetes prevention trials is unreliable. Diagnosis of non-diabetic hyperglycaemia and Type 2 diabetes should be confirmed by repeat testing. FPG results could help prioritise retesting. These findings do not apply to people classified as normal on a single test, who were not retested.
研究影响非糖尿病性高血糖和 2 型糖尿病诊断不一致的因素。
对约 10000 名糖尿病高危成年人进行 HbA 和空腹血浆葡萄糖(FPG)筛查。在最初 HbA≥42mmol/mol(≥6.0%)或 FPG≥6.1mmol/l 的 2208 名参与者中,在中位数 40 天后进行了复测。我们比较了第一次和第二次 HbA 结果,以及随后的非糖尿病性高血糖和 2 型糖尿病诊断,并调查了诊断不一致的预测因素。
在首次检测时患有非糖尿病性高血糖的 1463 名参与者和患有 2 型糖尿病的 394 名参与者中,分别有 28.4%和 21.1%在重复检测时出现了不一致的诊断。根据 HbA 和 FPG 标准,或仅根据 FPG 标准,将非糖尿病性高血糖和/或空腹血糖受损的初始诊断重新分类为 2 型糖尿病的可能性大于单独根据 HbA 进行初始分类。根据 HbA 和 FPG 标准进行初始 2 型糖尿病诊断的可能性小于单独根据 HbA 进行初始分类。年龄以及人体测量和生物学测量独立但不一致地预测了不一致的诊断和 HbA 的变化。
在糖尿病预防试验的筛查计划中,使用 HbA 的单次测量诊断非糖尿病性高血糖或 2 型糖尿病是不可靠的。非糖尿病性高血糖和 2 型糖尿病的诊断应通过重复检测来确认。FPG 结果可以帮助确定优先进行复测。这些发现不适用于在单次检测中被归类为正常的人,他们没有接受复测。