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22 June 2025 : Review article  

Linking Triglyceride-Glucose Index to Spontaneous Intracerebral Hemorrhage: Mechanisms and Predictive Insights

Jiahao Wang AEF 1,2, Yanling Zhou AEF 1,2, Yuruo Song EF 1,2, Qi Fang EF 1,2, Juan Xia EF 1,2, Pengxian Tao EF 3,4,5, Haizhong Ma EF 2,3,4, Dongzhi Zhang AEFG 6,2,3,4,7*

DOI: 10.12659/MSM.948695

Med Sci Monit 2025; 31:e948695

Table 1 Four large-scale randomized controlled trials on acute-phase blood pressure management in spontaneous intracerebral hemorrhage.

Trial namePrincipal investigatorSample sizeStudy objectives and methodologyMain findings
INTERACT1Anderson et al []14 Approximately 400 casesComparison of the safety and feasibility of intensive blood pressure lowering (target SBP <140 mmHg) vs standard blood pressure lowering (target SBP <180 mmHg)Intensive blood pressure lowering within 6 hours after hemorrhage is feasible and may be associated with a trend toward improved outcomes, providing a foundation for large-scale trials such as INTERACT2
INTERACT2Anderson et al []15 Approximately 2,800 casesParticipants were randomly assigned to either the intensive blood pressure lowering group (target SBP <140 mmHg) or the standard blood pressure lowering group (target SBP <180 mmHg), with functional outcomes assessed at 90 days using the modified Rankin scoreThere was no significant difference in the primary outcome between the two groups. However, the intensive blood pressure lowering group showed a trend toward improved outcomes in the distribution of the modified Rankin scores. Additionally, intensive blood pressure lowering did not increase the incidence of serious adverse events, supporting the feasibility of moderate intensive blood pressure control in the acute phase
ATACH1Qureshi et al []100 Pilot studyTo investigate the safety and feasibility of intensive blood pressure lowering in intracerebral hemorrhage (ICH)The results support the safety of intensive blood pressure lowering in acute ICH, providing a foundation for subsequent large-scale trials such as ATACH2
ATACH2Qureshi et al []16 Approximately 1000 casesSimilar to the INTERACT2 trial, this study compares intensive blood pressure lowering (target SBP <140 mmHg) with standard blood pressure lowering (target SBP <180 mmHg), assessing functional outcomes at 90 days and hematoma expansionThere was no significant difference between the two groups in terms of functional outcomes and hematoma expansion rate, raising doubts about the benefits of strictly maintaining SBP below 140 mmHg

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Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750