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Systemic inflammatory indices mediate the association between hyperuricemia and left ventricular hypertrophy:
Jingyuan Li1, Yang Xu1, Ruting Li2
1Department of Endocrinology and Metabolism, The Affiliated Hospital of Qingdao University, Qingdao, China.
Insights
Systemic inflammation, measured by SII and SIRI, is linked to left ventricular hypertrophy (LVH) in patients with hyperuricemia (HUA). These inflammation markers partially explain how high urate levels affect cardiac remodeling.
Area of Science:
- Cardiology
- Inflammation research
- Metabolic disorders
Background:
- Hyperuricemia (HUA) is linked to left ventricular hypertrophy (LVH), a cardiac injury marker.
- Systemic inflammation is implicated in ventricular remodeling.
- Systemic Immune-Inflammation Index (SII) and Systemic Inflammation Response Index (SIRI) may quantify inflammation.
Purpose of the Study:
- To investigate the association between SII, SIRI, and LVH in HUA patients.
- To explore the role of systemic inflammation in the relationship between serum urate and LVH.
Main Methods:
- Analysis of 3,632 HUA patients, excluding those with hypertension, diabetes, or advanced CKD.
- Calculation and log-transformation of SII and SIRI, followed by k-means clustering.
- Logistic regression, restricted cubic spline, and mediation analyses to assess associations and pathways.
Main Results:
- 12.5% of patients had LVH, associated with older age, female sex, higher SBP, urate, glucose, SII, SIRI, and lower eGFR, LVEF.
- Elevated SII and SIRI were independently associated with LVH.
- Systemic inflammation partially mediated the urate-LVH relationship (11.9% for SII, 29.9% for SIRI).
Conclusions:
- SII and SIRI are positively correlated with LVH in HUA patients.
- Systemic inflammation plays a partial mediating role in the urate-LVH relationship.
- Highlights inflammation's importance in hyperuricemia-related cardiovascular disease.
Aims:
Hyperuricemia (HUA) is associated with left ventricular hypertrophy (LVH), a reversible marker of cardiac injury. Systemic inflammation drives ventricular remodeling, and the systemic immune-inflammation index (SII) and systemic inflammation response index (SIRI) may reflect this process. This study investigated their associations with LVH in patients with HUA.
Methods:
We analyzed 3, 632 patients with HUA hospitalized between 2014 and 2024, excluding those with prior hypertension, diabetes, or advanced chronic kidney disease. Baseline demographic, biochemical, and echocardiographic data were collected. LVH was defined by sex-specific left ventricular mass index thresholds. SII and SIRI were calculated, log-transformed, and analyzed by k-means clustering. Associations with LVH were assessed using logistic regression, restricted cubic spline (RCS), and threshold effect models. Mediation analysis evaluated their role between serum urate and LVH.
Results:
Among all patients, 452 (12.5%) had LVH. Compared with non-LVH patients, those with LVH were older, more often female, and exhibited higher systolic blood pressure, serum urate, glucose, SII, and SIRI, and lower eGFR and LVEF (all p < 0.05). Elevated SII, SIRI, and high inflammatory patterns were independently associated with LVH (all p < 0.01). RCS revealed a nonlinear "J-shaped" association for lnSII with a threshold at 5.99, while lnSIRI showed a linear dose-response. Mediation analysis indicated systemic inflammation partially mediated the urate-LVH relationship (11.9% for lnSII, 29.9% for lnSIRI).
Conclusion:
In HUA patients, SII and SIRI are positively correlated with LVH and partially mediate the relationship between urate and cardiac remodeling, emphasizing the role of systemic inflammation in hyperuricemia related cardiovascular diseases.
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