Evidence map›Paper›PMID 41742084›Full record

ArticleBMC neurology2026

Association between admission high-sensitivity cardiac troponin T levels and clinical outcomes in acute intracerebral hemorrhage: a prospective cohort study.

Quoc Viet Bui, Anh Tuan Nguyen, Viet Hai Nguyen, Tien Dung Nguyen, Xuan Trung Vuong, Hong Son Trinh, Van Hung Nguyen, Minh Thu Vu, Viet Phuong Dao

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Article in BMC neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Quoc Viet BuiHanoi Medical University, Hanoi, Vietnam.
Anh Tuan NguyenHanoi Medical University, Hanoi, Vietnam.
Viet Hai NguyenVNU-University of Medicine and Pharmacy, Hanoi, Vietnam.
Tien Dung NguyenHanoi Medical University, Hanoi, Vietnam.
Xuan Trung VuongStroke Center, Bach Mai Hospital, Hanoi, Vietnam.
Hong Son TrinhHanoi Medical University, Hanoi, Vietnam.
Van Hung NguyenHanoi Medical University, Hanoi, Vietnam.
Minh Thu VuHanoi Medical University, Hanoi, Vietnam.
Viet Phuong DaoHanoi Medical University, Hanoi, Vietnam. daovietphuong85@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntracerebral hemorrhage remains one of the most devastating forms of stroke, associated with high mortality and disability. Cardiac injury following ICH, mediated through the brain-heart axis, may serve as a marker of disease severity. High-sensitivity cardiac troponin T, which rises rapidly after myocardial injury, has potential prognostic value in stroke-heart syndrome. The objective of this study was to determine whether elevated high-sensitivity cardiac troponin T levels at hospital admission is associated with early mortality, overall mortality, and poor functional outcome at 90 days in patients with acute intracerebral hemorrhage.

methodsThis is a prospective cohort study, which enrolled 256 patients with acute ICH admitted within 24 h of onset to the Stroke Center, Bach Mai Hospital, from February 2025 to June 2025. Baseline characteristics, hematoma features, comorbidities, and high-sensitivity cardiac troponin T levels were collected immediately upon admission. Clinical outcomes included early mortality (< seven days), overall mortality, and poor functional outcome (modified Rankin Scale score 4-6) were evaluated. Multivariate regression identified independent associations.

resultsElevated high-sensitivity cardiac troponin T levels was observed in 88 patients (34.4%). These patients had significantly lower Glasgow Coma Scale scores and larger hematoma volumes. Poor functional outcome occurred in 80.7% vs., 53.6% (p-value < 0.001), overall mortality in 65.9% vs., 33.9% (p-value < 0.001), and early mortality in 54.5% vs. 22.6% (p-value < 0.001) when comparing elevated and non-elevated high-sensitivity cardiac troponin T patients, respectively. After multivariable adjustment, elevated high-sensitivity cardiac troponin T (hs-cTnT) was independently associated with poor functional outcome (OR 2.41; 95% CI 1.06-5.49) and early mortality (OR 2.85; 95% CI 1.10-7.42). An association with overall mortality was also observed (OR 2.27; 95% CI 0.97-5.27), although this did not reach statistical significance. In time-to-event analyses, patients with elevated hs-cTnT experienced a significantly shorter restricted mean survival time compared with those without hs-cTnT elevation (13.9 vs. 22.4 days), corresponding to a mean survival difference of approximately 8.5 days (95% CI -11.2 to -5.8; p < 0.001).

conclusionAdmission elevated high-sensitivity cardiac troponin T was associated with adverse outcomes in acute primary intracerebral hemorrhage and showed a notable association with early mortality.

Indexed as

Cerebral HemorrhageTroponin TAgedAged, 80 and overBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedPrognosisProspective StudiesBiomarkersTroponin TFunctional outcome prognosisHigh-sensitivity cardiac troponin TIntracerebral hemorrhageMortality predictionStroke-heart syndrome

Identifiers

PMID41742084
PMCPMC13001354

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