Key result
Higher CRP-TyG index linked to ~25% greater risk of depressive symptoms per SD.
Why the study?
Prospective evidence on whether the C-reactive protein-triglyceride-glucose index, reflecting inflammatory-metabolic dysregulation, predicts incident depressive symptoms in aging populations is limited.
Does a higher baseline CRP-TyG index predict an increased risk of incident depressive symptoms in older adults?
Population
2,813 depression-free participants aged ≥ 50 years in ELSA
Comparison
Higher vs lower baseline CTI (per 1-SD increase)
Design
Nationally representative prospective cohort study
Follow-up
Eight-year follow-up (through Wave 8)
Authors
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May support CTI as a depressive risk marker in older adults; hypothesis-generating and requires validation before clinical adoption.
Cohort (n=2,813)
Does a higher baseline CRP-TyG index predict an increased risk of incident depressive symptoms in older adults?
Hazard Ratio: 1.253 (95% CI 1.002–1.479)
p-value: p=0.035
Higher baseline CRP-TyG index is prospectively associated with an increased risk of incident depressive symptoms in older adults, suggesting its potential as a scalable risk biomarker.
Guo et al. (2026) conducted a cohort in incident depressive symptoms (n=2,813). CRP-TyG index (CTI) was evaluated on incident depressive symptoms (HR 1.253, 95% CI 1.002-1.479, p=0.035). Each 1-SD increase in baseline CRP-TyG index was associated with a higher risk of incident depressive symptoms in older adults (HR 1.253; 95% CI 1.002-1.479; p=0.035).
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