Scholarlink

Objective <p>To investigate the relationship between the triglyceride-glucose (TyG) index and symptomatic intracranial atherosclerotic stenosis (sICAS) in non-diabetic patients.</p> Methods <p>This retrospective study analyzed 968 nondiabetic acute ischemic stroke (AIS) patients admitted between January 2022 and December 2024. Intergroup differences between the sICAS group and the non-sICAS group were analyzed. The TyG index was calculated, and stratified into TyG tertiles (T1–T3). Multivariable logistic regression models adjusted for age, sex, smoking status, alcohol use, hypertension status, BMI, and lipid profiles were used to assess associations with sICAS, stenosis severity, and plaque vulnerability. Restricted cubic splines explore nonlinear relationships.</p> Results <p>Among the 968 included patients, the median age was 58 (IQR 50–66) years, and 43.39% were male. The median TyG index was 8.96 (IQR 8.77, 9.13). Patients with sICAS presented significantly higher total cholesterol (TC) levels and TyG index values, and lower high-density lipoprotein (HDL) levels. The high-TyG group presented a significantly greater prevalence of male, sex, a history of smoking and hypertension, an elevated body mass index (BMI), and lower HDL levels. An elevated TyG index was significantly associated with sICAS, moderate and severe stenosis and vulnerable plaques. This association was maintained after adjusting for age, sex, smoking, alcohol use, hypertension, BMI, TC, HDL, and low-density lipoprotein (LDL) levels. Multivariable-adjusted spline regression models revealed that a progressively increasing risk of sICAS, moderate and severe stenosis and vulnerable plaques was related to an elevated TyG index.</p> Conclusion <p>An elevated TyG index is significantly associated with sICAS and independently associated with severe intracranial arterial stenosis and vulnerable plaques in nondiabetic AIS patients.</p>

错误：搜索内容不能为空，请输入英文关键词
错误：关键词超出字数限制，请精简
高级检索

Association between the triglyceride-glucose index and symptomatic intracranial atherosclerotic stenosis in nondiabetic patients: a retrospective study

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年8月8日

查看全文
  • Yang Yang,
  • Chunhao Mei,
  • Xiaoning Guo,
  • Bojun Han,
  • Qingguang Wang

摘要

Objective

To investigate the relationship between the triglyceride-glucose (TyG) index and symptomatic intracranial atherosclerotic stenosis (sICAS) in non-diabetic patients.

Methods

This retrospective study analyzed 968 nondiabetic acute ischemic stroke (AIS) patients admitted between January 2022 and December 2024. Intergroup differences between the sICAS group and the non-sICAS group were analyzed. The TyG index was calculated, and stratified into TyG tertiles (T1–T3). Multivariable logistic regression models adjusted for age, sex, smoking status, alcohol use, hypertension status, BMI, and lipid profiles were used to assess associations with sICAS, stenosis severity, and plaque vulnerability. Restricted cubic splines explore nonlinear relationships.

Results

Among the 968 included patients, the median age was 58 (IQR 50–66) years, and 43.39% were male. The median TyG index was 8.96 (IQR 8.77, 9.13). Patients with sICAS presented significantly higher total cholesterol (TC) levels and TyG index values, and lower high-density lipoprotein (HDL) levels. The high-TyG group presented a significantly greater prevalence of male, sex, a history of smoking and hypertension, an elevated body mass index (BMI), and lower HDL levels. An elevated TyG index was significantly associated with sICAS, moderate and severe stenosis and vulnerable plaques. This association was maintained after adjusting for age, sex, smoking, alcohol use, hypertension, BMI, TC, HDL, and low-density lipoprotein (LDL) levels. Multivariable-adjusted spline regression models revealed that a progressively increasing risk of sICAS, moderate and severe stenosis and vulnerable plaques was related to an elevated TyG index.

Conclusion

An elevated TyG index is significantly associated with sICAS and independently associated with severe intracranial arterial stenosis and vulnerable plaques in nondiabetic AIS patients.