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Updated: Oct 18, 2025

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
CHLD score, a new score based on traditional risk factor evaluation and long-term cardiovascular outcomes in patients
Klaudia Gieszczyk-Strózik1,2, Maciej T Wybraniec3,4, Małgorzata Widuchowska2,5
1First Department of Cardiology, School of Medicine in Katowice, Medical University of Silesia, 47 Ziołowa St., 40-635, Katowice, Poland.
Insights
A new score combining chronic kidney disease, hypertension, hyperlipidemia, and diabetes (CHLD) effectively predicts major adverse cardiovascular events (MACE) in systemic sclerosis patients without pulmonary hypertension.
Area of Science:
- Cardiology
- Rheumatology
- Clinical Prediction Models
Background:
- Systemic sclerosis (SSc) patients without pulmonary arterial hypertension face significant cardiovascular risks.
- Identifying reliable predictors of major adverse cardiovascular events (MACE) is crucial for managing SSc patients.
- Existing risk stratification models may not fully capture cardiovascular risk in this specific SSc population.
Purpose of the Study:
- To identify independent predictors of MACE in patients with SSc, excluding those with pulmonary arterial hypertension.
- To develop and validate a predictive score for long-term cardiovascular outcomes in this patient group.
Main Methods:
- A cohort of 68 SSc patients without pulmonary arterial hypertension was followed for a median of 99 months.
- Baseline assessments included cardiovascular risk factors, 6-min walk test, echocardiography, and GDF-15 levels.
- MACE was defined as death, myocardial infarction, revascularization, or heart failure hospitalization.
Main Results:
- Chronic kidney disease, lung fibrosis, and GDF-15 were identified as independent MACE predictors at baseline.
- The developed CHLD score (Chronic kidney disease, Hypertension, hyperLipidaemia, Diabetes mellitus) emerged as the sole independent predictor of MACE.
- Each point increase in the CHLD score significantly elevated the risk of MACE (HR 3.46).
Conclusions:
- The CHLD score is a reliable and independent predictor of long-term MACE in SSc patients without pulmonary arterial hypertension.
- Integrating traditional risk factors into the CHLD score improves cardiovascular risk assessment in this population.
- This score can aid in proactive management and risk stratification for SSc patients.
Abstract:
The aim of the study was to assess the predictors of major adverse cardiovascular events (MACE) in patients with systemic sclerosis (SSc) without pulmonary arterial hypertension. The study comprised 68 patients with SSc who were followed up for the median time of 99 (96; 107) months. The main exclusion criteria involved tricuspid regurgitation maximal velocity > 2.8 m/s and structural heart disease. At baseline the patients underwent clinical assessment of cardiovascular risk factors, 6-min walk test, transthoracic echocardiography and biomarker testing, including growth differentiation factor 15 (GDF-15). The primary composite endpoint was onset of MACE defined as death, myocardial infarction, myocardial revascularization and hospitalization for heart failure. The follow-up consisted of outpatient visits at 1 year intervals and telephone interview every 6 months. The baseline analysis revealed that chronic kidney disease (HR 28.13, 95%CI 4.84-163.38), lung fibrosis on high resolution computed tomography (HR 4.36, 95%CI 1.04-18.26) and GDF-15 concentration (unit HR 1.0006, 95%CI 1.0002-1.0010) were independent predictors of MACE occurrence. CHLD (Chronic kidney disease, Hypertension, hyperLipidaemia, Diabetes mellitus) score was formulated which assigned 1 point for the presence of arterial hypertension, hyperlipidaemia, diabetes mellitus and chronic kidney disease. After inclusion of CHLD score in Cox proportional model, it remained the only independent predictor of MACE onset (unit HR per 1 point 3.46; 95%CI 2.06-5.82, p < 0.0001). Joint assessment of traditional risk factors in the form of CHLD score may serve as a reliable predictor of long-term outcome in patients with SSc without pulmonary arterial hypertension.
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