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单点胰岛素敏感性估算值(SPISE)为 5.4 时,可较好地预测肥胖青少年的代谢综合征和胰岛素抵抗。

A Single-Point Insulin Sensitivity Estimator (SPISE) of 5.4 is a good predictor of both metabolic syndrome and insulin resistance in adolescents with obesity.

机构信息

Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, Santiago, Chile.

Departamento de Gastroenterología y Nutrición Pediátrica, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

Front Endocrinol (Lausanne). 2023 Feb 8;14:1078949. doi: 10.3389/fendo.2023.1078949. eCollection 2023.

Abstract

BACKGROUND

The Single-Point Insulin Sensitivity Estimator (SPISE) is a biomarker of insulin sensitivity estimated using BMI and triglycerides and high-density lipoprotein cholesterol. We assessed the accuracy of SPISE to screen obesity-related cardiometabolic risk in children and adolescents.

METHOD

Cross-sectional validation study for a screening test in a sample of =725 children and adolescents from an obesity clinic. Weight, height, waist circumference, blood arterial pressure, lipid profile, glucose, insulin and Tanner stage were measured. BMI, BMI for-age-and sex (BAZ), and HOMA-IR were estimated. HOMA-IR values ≥2.1 and ≥3.3 were considered IR in Tanner I-II, ≥3.3 for Tanner III-IV and ≥2.6 for Tanner V, respectively. Metabolic Syndrome (MetS) was diagnosed with the Cook phenotype. SPISE was estimated according to the following algorithm: [600* HDL^0.185/(TG^0.2* BMI^1.338)]. The optimal SPISE cut points for IR and MetS prediction were determined by ROC curve analysis.

RESULTS

In prepubertal obese patients (9.2 ± 2.1y; 18.4% males), the prevalence of IR and MetS was 28.2% y 46.9%, respectively; 58% had severe obesity (BAZ ≥4 ). In pubertal obese patients (12.6 ± 1.8y; 57% males), the prevalence of IR and MetS was 34.1% and 55.3%, respectively; 34% had severe obesity. In prepubertal children, a SPISE of 6.3 showed the highest sensitivity (73.2%) and specificity (80%) to screen individuals with IR (AUC: 0.80; LR +: 3.3). Likewise, a SPISE of 5.7 got the highest sensitivity (82.6%) and specificity (86.1%) to screen patients with MetS (AUC: 0.87; LR +: 5.4). In pubertal patients, a SPISE of 5.4 showed the highest sensitivity and specificity to screen children and adolescents with both IR (Sn: 76.1%; Sp: 77.5%; AUC: 0.8; LR +: 3.1) and MetS (Sn: 90.4%; Sp: 76.1%; AUC: 0.90; LR +: 3.5).

CONCLUSION

In children and adolescents with obesity, SPISE has good or very good performance in predicting IR and MetS. SPISE may be considered a relatively simple and low-cost diagnosis tool that can be helpful to identify patients with greater biological risk. In adolescents with obesity, the same cut point allows identification of those at higher risk of both IR and MetS.

摘要

背景

单点胰岛素敏感性估算器(SPISE)是一种使用 BMI 和甘油三酯及高密度脂蛋白胆固醇估算的胰岛素敏感性生物标志物。我们评估了 SPISE 在筛查儿童和青少年肥胖相关代谢风险方面的准确性。

方法

对来自肥胖诊所的=725 名儿童和青少年样本进行横断面验证研究。测量体重、身高、腰围、动脉血压、血脂谱、血糖、胰岛素和 Tanner 分期。估算 BMI、BMI 年龄性别(BAZ)和 HOMA-IR。Tanner I-II 期 HOMA-IR 值≥2.1 和≥3.3 被认为存在胰岛素抵抗,Tanner III-IV 期 HOMA-IR 值≥3.3 和 Tanner V 期 HOMA-IR 值≥2.6 被认为存在胰岛素抵抗。用 Cook 表型诊断代谢综合征(MetS)。SPISE 按照以下算法估算:[600HDL^0.185/(TG^0.2BMI^1.338)]。通过 ROC 曲线分析确定预测 IR 和 MetS 的最佳 SPISE 截断点。

结果

在青春前期肥胖患者(9.2±2.1 岁;18.4%男性)中,IR 和 MetS 的患病率分别为 28.2%和 46.9%;58%有严重肥胖(BAZ≥4)。在青春期肥胖患者(12.6±1.8 岁;57%男性)中,IR 和 MetS 的患病率分别为 34.1%和 55.3%;34%有严重肥胖。在青春前期儿童中,SPISE 为 6.3 时,对筛查 IR 个体的敏感性(73.2%)和特异性(80%)最高(AUC:0.80;LR +:3.3)。同样,SPISE 为 5.7 时,对筛查 MetS 患者的敏感性(82.6%)和特异性(86.1%)最高(AUC:0.87;LR +:5.4)。在青春期患者中,SPISE 为 5.4 时,对同时存在 IR 和 MetS 的儿童和青少年的敏感性和特异性最高(Sn:76.1%;Sp:77.5%;AUC:0.8;LR +:3.1)和 MetS(Sn:90.4%;Sp:76.1%;AUC:0.90;LR +:3.5)。

结论

在肥胖儿童和青少年中,SPISE 在预测 IR 和 MetS 方面具有较好或很好的性能。SPISE 可被视为一种相对简单且低成本的诊断工具,有助于识别具有更高生物学风险的患者。在肥胖青少年中,相同的截断点可以识别出具有更高 IR 和 MetS 风险的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/539b/9945119/9d7a408ff790/fendo-14-1078949-g001.jpg

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