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适当的筛查间隔时间以检测慢性代谢性疾病的发生。

Appropriate screening interval to detect the development of chronic metabolic diseases.

机构信息

Division of Cardiology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

Department of Medicine, MetroWest Medical Center, Framingham, MA, USA.

出版信息

Diabetes Res Clin Pract. 2023 May;199:110648. doi: 10.1016/j.diabres.2023.110648. Epub 2023 Apr 3.

Abstract

AIMS

We conducted a cohort study to determine the screening intervals of metabolic disorders.

METHOD

Participants without diabetes mellitus (DM), hypertension (HTN), dyslipidemia, and abdominal obesity who underwent health examinations (2005-2019) in Korea were included. Participants were grouped according to baseline fasting glucose, LDL-C level, blood pressure (BP), and waist circumference (WC). The time to develop metabolic disorders and the percentile of survival time was assessed in each group.

RESULT

The median follow-up duration was 4.94 years (n=222,413; mean age 37.13 ± 7.49 years). After 8.32(95 %CI 8.22-8.41), 3.01(2.89-3.31), and 1.11(1.03-1.25) years, 10 % of participants developed DM in fasting glucose levels of 100-110, 110-120, and 120-125 mg/dL, respectively. After 8.40(8.33-8.45), 6.33(6.20-6.47), and 1.99(1.97-2.00) years, 10 % developed HTN in BP 120/70, 120/70-130/80, and 130/80-140/90 mmHg, respectively. After 5.99(5.94-6.04), 2.84(2.77-2.90), and 1.36(1.30-1.44) years, 10 % developed dyslipidemia in LDL-C 100-120, 120-140, and 140-160 mg/dL, respectively. After 4.62(4.41-4.80) and 1.67(1.64-1.69) years, 10 % developed abdominal obesity in baseline WC < 80(Women;W)/85(Men;M) and < 85(W)/90(M) cm, respectively.

CONCLUSION

In adults aged 30-40, the screening interval of metabolic disorders should be individualized based on the baseline metabolic derangement. An individual with borderline values may need an annual screening.

摘要

目的

我们进行了一项队列研究,以确定代谢紊乱的筛查间隔。

方法

纳入了在韩国接受健康检查(2005-2019 年)且无糖尿病(DM)、高血压(HTN)、血脂异常和腹型肥胖的参与者。根据基线空腹血糖、LDL-C 水平、血压(BP)和腰围(WC)将参与者分为不同组。评估了每组代谢紊乱的发病时间和生存时间的百分位数。

结果

中位随访时间为 4.94 年(n=222413;平均年龄 37.13±7.49 岁)。在空腹血糖水平为 100-110、110-120 和 120-125mg/dL 的情况下,分别在 8.32(95%CI 8.22-8.41)、3.01(2.89-3.31)和 1.11(1.03-1.25)年后,有 10%的参与者发展为 DM。在 BP 为 120/70、120/70-130/80 和 130/80-140/90mmHg 的情况下,分别在 8.40(8.33-8.45)、6.33(6.20-6.47)和 1.99(1.97-2.00)年后,有 10%的参与者发展为 HTN。在 LDL-C 为 100-120、120-140 和 140-160mg/dL 的情况下,分别在 5.99(5.94-6.04)、2.84(2.77-2.90)和 1.36(1.30-1.44)年后,有 10%的参与者发展为血脂异常。在基线 WC<80(女性;W)/85(男性;M)和<85(W)/90(M)cm 的情况下,分别在 4.62(4.41-4.80)和 1.67(1.64-1.69)年后,有 10%的参与者发展为腹型肥胖。

结论

在 30-40 岁的成年人中,应根据基线代谢紊乱情况个体化筛查代谢紊乱的间隔。边界值的个体可能需要每年筛查一次。

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