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Q-Score: development of a new metric for continuous glucose monitoring that enables stratification of antihyperglycaemic therapies

机译:Q-Score:开发一种用于连续血糖监测的新指标,该指标可实现抗高血糖疗法的分层

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Background Continuous glucose monitoring (CGM) has revolutionised diabetes management. CGM enables complete visualisation of the glucose profile, and the uncovering of metabolic ‘weak points’. A standardised procedure to evaluate the complex data acquired by CGM, and to create patient-tailored recommendations has not yet been developed. We aimed to develop a new patient-tailored approach for the routine clinical evaluation of CGM profiles. We developed a metric allowing screening for profiles that require therapeutic action and a method to identify the individual CGM parameters with improvement potential. Methods Fifteen parameters frequently used to assess CGM profiles were calculated for 1,562 historic CGM profiles from subjects with type 1 or type 2 diabetes. Factor analysis and varimax rotation was performed to identify factors that accounted for the quality of the profiles. Results We identified five primary factors that determined CGM profiles (central tendency, hyperglycaemia, hypoglycaemia, intra- and inter-daily variations). One parameter from each factor was selected for constructing the formula for the screening metric, (the ‘Q-Score’). To derive Q-Score classifications, three diabetes specialists independently categorised 766 CGM profiles into groups of ‘very good’, ‘good’, ‘satisfactory’, ‘fair’, and ‘poor’ metabolic control. The Q-Score was then calculated for all profiles, and limits were defined based on the categorised groups (<4.0, very good; 4.0–5.9, good; 6.0–8.4, satisfactory; 8.5–11.9, fair; and ≥12.0, poor). Q-Scores increased significantly (P <0.01) with increasing antihyperglycaemic therapy complexity. Accordingly, the percentage of fair and poor profiles was higher in insulin-treated compared with diet-treated subjects (58.4% vs. 9.3%). In total, 90% of profiles categorised as fair or poor had at least three parameters that could potentially be optimised. The improvement potential of those parameters can be categorised as ‘low’, ‘moderate’ and ‘high’. Conclusions The Q-Score is a new metric suitable to screen for CGM profiles that require therapeutic action. Moreover, because single components of the Q-Score formula respond to individual weak points in glycaemic control, parameters with improvement potential can be identified and used as targets for optimising patient-tailored therapies.
机译:背景技术连续血糖监测(CGM)彻底改变了糖尿病的治疗方法。 CGM可以使葡萄糖分布图完整可视化,并揭示新陈代谢的“弱点”。尚未开发出评估CGM获取的复杂数据并创建针对患者的推荐的标准化程序。我们旨在开发一种针对患者的新方法,用于CGM概况的常规临床评估。我们开发了一种度量标准,可以筛选需要治疗作用的概况,以及一种确定具有改善潜力的个体CGM参数的方法。方法从1型或2型糖尿病患者的1,562例历史CGM谱中计算出15个经常用​​于评估CGM谱的参数。进行因子分析和varimax旋转以识别占轮廓质量的因子。结果我们确定了决定CGM分布的五个主要因素(集中趋势,高血糖,低血糖,每日内和每日间变化)。从每个因子中选择一个参数来构建筛选指标的公式(“ Q评分”)。为了获得Q-Score分类,三位糖尿病专家将766个CGM配置文件分别归类为“非常好”,“好”,“满意”,“一般”和“差”的代谢控制。然后计算所有配置文件的Q分数,并根据分类的组定义限制(<4.0,非常好; 4.0–5.9,好; 6.0–8.4,好; 8.5–11.9,好;≥12.0,差)。随着抗高血糖治疗复杂性的增加,Q评分显着增加(P <0.01)。因此,与饮食治疗的受试者相比,接受胰岛素治疗的受试者的公平和不良状况所占的百分比更高(58.4%比9.3%)。总体而言,归类为“一般”或“差”的个人资料中有90%具有至少三个可以优化的参数。这些参数的改进潜力可分为“低”,“中”和“高”。结论Q-Score是适用于筛选需要治疗作用的CGM概况的新指标。此外,由于Q-Score公式的单个成分对血糖控制中的各个弱点有反应,因此可以确定具有改善潜力的参数,并将其用作优化患者量身定制的治疗方法的目标。

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