AMRA Medical AB, Linköping, Sweden.
Research Centre for Optimal Health, University of Westminster, London, UK.
Obesity (Silver Spring). 2019 Jul;27(7):1190-1199. doi: 10.1002/oby.22510. Epub 2019 May 16.
This study performed individual-centric, data-driven calculations of propensity for coronary heart disease (CHD) and type 2 diabetes (T2D), utilizing magnetic resonance imaging-acquired body composition measurements, for sub-phenotyping of obesity and nonalcoholic fatty liver disease (NAFLD).
A total of 10,019 participants from the UK Biobank imaging substudy were included and analyzed for visceral and abdominal subcutaneous adipose tissue, muscle fat infiltration, and liver fat. An adaption of the k-nearest neighbors algorithm was applied to the imaging variable space to calculate individualized CHD and T2D propensity and explore metabolic sub-phenotyping within obesity and NAFLD.
The ranges of CHD and T2D propensity for the whole cohort were 1.3% to 58.0% and 0.6% to 42.0%, respectively. The diagnostic performance, area under the receiver operating characteristic curve (95% CI), using disease propensities for CHD and T2D detection was 0.75 (0.73-0.77) and 0.79 (0.77-0.81). Exploring individualized disease propensity, CHD phenotypes, T2D phenotypes, comorbid phenotypes, and metabolically healthy phenotypes were found within obesity and NAFLD.
The adaptive k-nearest neighbors algorithm allowed an individual-centric assessment of each individual's metabolic phenotype moving beyond discrete categorizations of body composition. Within obesity and NAFLD, this may help in identifying which comorbidities a patient may develop and consequently enable optimization of treatment.
本研究利用磁共振成像获取的身体成分测量数据,进行个体中心、数据驱动的冠心病(CHD)和 2 型糖尿病(T2D)倾向计算,对肥胖和非酒精性脂肪性肝病(NAFLD)进行亚表型分析。
共纳入英国生物银行影像学子研究的 10019 名参与者,并对内脏和腹部皮下脂肪组织、肌肉脂肪浸润和肝脏脂肪进行分析。采用 k-最近邻算法的改编版对影像学变量空间进行计算,以计算个体的 CHD 和 T2D 倾向,并探索肥胖和 NAFLD 内的代谢亚表型。
整个队列的 CHD 和 T2D 倾向范围分别为 1.3%至 58.0%和 0.6%至 42.0%。使用疾病倾向检测 CHD 和 T2D 的诊断性能,即受试者工作特征曲线下面积(95%CI)为 0.75(0.73-0.77)和 0.79(0.77-0.81)。在肥胖和 NAFLD 内探索个体疾病倾向、CHD 表型、T2D 表型、合并表型和代谢健康表型。
自适应 k-最近邻算法允许对每个个体的代谢表型进行个体中心评估,超越了身体成分的离散分类。在肥胖和 NAFLD 中,这可能有助于识别患者可能发展的哪些合并症,并因此能够优化治疗。