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Diastolic Dysfunction in Systemic Sclerosis: Risk Factors and Impact on Mortality
Alicia M Hinze1, Jamie Perin2, Adrianne Woods3
1Mayo Clinic, Rochester, Minnesota.
Insights
Diastolic dysfunction (DD) is a significant risk factor for mortality in systemic sclerosis (SSc) patients. Addressing modifiable risks like coronary artery disease and obesity may reduce SSc mortality.
Area of Science:
- Cardiology
- Rheumatology
- Internal Medicine
Background:
- Systemic sclerosis (SSc) is a complex autoimmune disease with significant cardiovascular implications.
- Diastolic dysfunction (DD) is a recognized complication, but its independent risk factors and impact on mortality in SSc require further elucidation.
Purpose of the Study:
- To identify independent risk factors for developing diastolic dysfunction (DD) in patients with systemic sclerosis (SSc).
- To evaluate the impact of DD on overall mortality in the SSc patient population.
Main Methods:
- A cohort of 806 SSc patients with available echocardiograms was analyzed.
- Logistic regression identified DD risk factors, while Cox proportional hazards models assessed survival.
- Prospective data collection included SSc disease characteristics and clinical risk factors.
Main Results:
- Diastolic dysfunction (DD) was present in 18.6% of SSc patients.
- Independent risk factors for DD included older age, coronary artery disease, obesity, longer SSc duration, reduced diffusing capacity for carbon monoxide, and history of scleroderma renal crisis.
- Anti-Scl-70 positivity and severe gastrointestinal disease were associated with reduced DD risk.
- DD independently increased the risk of mortality (HR 1.69).
Conclusions:
- Diastolic dysfunction (DD) is an independent predictor of increased mortality in patients with systemic sclerosis (SSc).
- Targeting modifiable risk factors such as coronary artery disease and obesity is crucial for mitigating mortality risk in SSc patients.
Objective:
To determine the independent risk factors for diastolic dysfunction (DD) in patients with systemic sclerosis (SSc) and to evaluate the impact of DD on mortality.
Methods:
SSc patients enrolled in the Johns Hopkins Scleroderma Center Cohort between November 1, 2006 and November 1, 2017 with ≥1 analyzable 2-dimensional (2-D) echocardiogram in our system were included (n = 806). DD risk factors and SSc disease characteristics were prospectively obtained, and the presence or absence of DD was determined using the most recent 2-D echocardiogram. Logistic regression models examined associations between clinical risk factors and DD, and Cox proportional hazards models were used to assess survival.
Results:
DD was present in 18.6% of participants. The majority of participants were female (84%) with a median age of 58.4 years (interquartile range 48.8-68.1). Older age (odds ratio [OR] 1.12 [95% confidence interval (95% CI) 1.09-1.15], P < 0.001), coronary artery disease (OR 3.69 [95% CI 1.52-8.97], P = 0.004), obesity (OR 4.74 [95% CI 2.57-8.74], P < 0.001), longer SSc disease duration (OR 1.04 [95% CI 1.01-1.06], P = 0.004), diffusing capacity for carbon monoxide ≤60% of predicted (OR 2.41 [95% CI 1.40-4.16], P = 0.002), and history of scleroderma renal crisis (OR 3.18 [95% CI 1.12-9.07], P = 0.031) were all independently associated with an increased risk of DD. Anti-Scl-70 positivity (OR 0.49 [95% CI 0.26-0.93], P = 0.03) and severe gastrointestinal disease (OR 0.48 [95% CI 0.30-0.79], P = 0.004) were associated with a reduced risk of DD. The presence of DD was independently associated with an increase in the risk of mortality (hazard ratio 1.69 [95% CI 1.07-2.68], P = 0.027).
Conclusion:
DD is independently associated with an increased risk of mortality in patients with SSc. Potentially modifiable risk factors, including coronary artery disease and obesity, should be addressed in patients with SSc to reduce mortality risk.
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