Key result
Diabetes and high CTI linked to ~95% higher mortality in ADHF with stage 4 CKM.
Why the study?
Risk stratification in stage 4 cardiovascular–kidney–metabolic syndrome with acute decompensated heart failure remains challenging due to influences of dysglycaemia, triglyceride-related metabolic disturbance, systemic inflammation, and adiposity-related risk.
Does the C-reactive protein–triglyceride–glucose index (CTI) combined with diabetes status predict all-cause mortality and MACCEs in patients with stage 4 CKM syndrome hospitalized for ADHF?
Cohort (n=2,000)
No
Does the C-reactive protein–triglyceride–glucose index (CTI) combined with diabetes status predict all-cause mortality and MACCEs in patients with stage 4 CKM syndrome hospitalized for ADHF?
In patients with stage 4 CKM syndrome hospitalized for ADHF, elevated CTI combined with diabetes identifies a subgroup at particularly high risk for mortality and MACCEs.
Answers are grounded in this paper and cite their sources.
Diabetes plus high CTI marks highest mortality risk in stage 4 CKM with ADHF; supports CTI for stratification but remains hypothesis-generating.
Background Cardiovascular–kidney–metabolic (CKM) syndrome integrates metabolic dysfunction, kidney disease, and cardiovascular disease. In stage 4 CKM syndrome with acute decompensated heart failure (ADHF), prognosis may be influenced by dysglycaemia, triglyceride-related metabolic disturbance, systemic inflammation, and adiposity-related risk, yet risk stratification remains challenging. We evaluated whether the C-reactive protein–triglyceride–glucose index (CTI), a routinely available inflammatory-metabolic marker, refines risk stratification beyond diabetes status and related inflammatory-metabolic biomarkers in patients with stage 4 CKM syndrome and ADHF. Methods This single-centre retrospective cohort included 2,000 eligible patients hospitalized for ADHF with CKM stage 4. CTI was calculated as 0.412 × ln[CRP (mg/L)] + ln[TG (mg/dL) × FPG (mg/dL) / 2]. High CTI was defined using the cohort-specific upper-tertile threshold (CTI ≥ 9.50). Patients were categorized as non-DM + low CTI, non-DM + high CTI, DM + low CTI, or DM + high CTI. Outcomes were all-cause mortality and major adverse cardiac and cerebrovascular events (MACCEs). Results During a median follow-up of 532 days, 366 deaths (18.3%) and 551 MACCEs (27.6%) occurred. Compared with non-DM + low CTI, non-DM + high CTI was associated with higher risks of all-cause mortality (HR 1.54, 95% CI 1.15–2.06) and MACCEs (HR 1.37, 95% CI 1.08–1.75). DM + low CTI was not significantly associated with either outcome, whereas DM + high CTI had the highest risks of all-cause mortality (HR 1.95, 95% CI 1.47–2.58) and MACCEs (HR 1.91, 95% CI 1.51–2.41). CTI showed approximately linear associations with both outcomes, without significant interaction by diabetes status. Adding CTI to the clinical model plus diabetes status yielded modest improvements in discrimination (ΔC-index = 0.018 for mortality and 0.016 for MACCEs), exceeding those of the evaluated biomarker models. Sensitivity analyses generally supported the primary findings. Conclusion In patients with stage 4 CKM syndrome hospitalized for ADHF, elevated CTI was associated with higher risks of all-cause mortality and MACCEs, with the greatest risk in patients with both diabetes and high CTI. CTI may be a candidate adjunctive marker for risk refinement; external validation is required before clinical implementation.
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Wang et al. (2026) conducted a cohort in Stage 4 cardiovascular-kidney-metabolic syndrome with acute decompensated heart failure (n=2,000). Diabetes mellitus and high C-reactive protein-triglyceride-glucose index (CTI) vs. No diabetes mellitus and low CTI was evaluated on All-cause mortality (HR 1.95, 95% CI 1.47-2.58, p=<0.001). In patients hospitalized for acute decompensated heart failure with stage 4 cardiovascular-kidney-metabolic syndrome, having both diabetes and a high CTI was associated with a 95% increased risk of all-cause mortality (HR 1.95) compared to non-diabetics with low CTI.
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