# Frailty and Cognitive Function After the Age of 40 in Adults With Moderate or Severe Congenital Heart Disease

**Authors:** Sandra Skogby, Christina Christersson, Joanna Hlebowicz, Zacharias Mandalenakis, Eva Goossens, Adrienne H. Kovacs, Liesbet Van Bulck, Koen Luyckx, Philip Moons, Camilla Sandberg, Bengt Johansson

PMC · DOI: 10.1016/j.cjcpc.2025.07.003 · CJC Pediatric and Congenital Heart Disease · 2025-08-05

## TL;DR

The study finds that adults with moderate or severe congenital heart disease have similar rates of frailty and cognitive issues as healthy people of the same age.

## Contribution

It compares frailty and cognitive function in adults with CHD and controls, revealing no significant differences.

## Key findings

- Adults with CHD and controls had similar Montreal Cognitive Assessment scores.
- The prevalence of prefrailty/frailty was not statistically different between the groups.

## Abstract

Decades of progress in care and treatment for congenital heart disease (CHD) has gradually shifted the research focus from initial survival to long-term prognosis and the ageing of adults with CHD. Knowledge about the ageing adult with CHD will guide interventions to safeguard the quality of life across the life course. The present study compares the prevalence of frailty and cognitive dysfunction between adults with CHD and a control group.

Using a multicentre design, we compared adults with moderate or complex CHD aged ≥40 years, equally distributed across the age groups 40-49, 50-59, and >60 years, with age- and sex-matched controls. We assessed frailty phenotypes using the Fried method and cognitive dysfunction using the Montreal Cognitive Assessment tool.

In total, 156 adults with CHD (56.0 ± 10.4 years, 54.4% male) and 86 controls (55.6 ± 11.2 years, 55.8% male) were included in the study. Adults with CHD and controls did not differ in terms of mean score on the Montreal Cognitive Assessment (mean score 27.1 vs 26.9, P = 0.59). Similarly, there was no statistical difference in the prevalence of prefrailty/frailty between adults with CHD and controls (36.5% vs 29.0%, P = 0.26).

Prevalence rates of cognitive dysfunction and frailty were similar between adults with CHD and age-matched controls. As more patients, particularly those with complex heart lesions, reach older ages, the prevalence of cognitive impairment and frailty may change.

## Linked entities

- **Diseases:** congenital heart disease (MONDO:0005453)

## Full-text entities

- **Diseases:** Cognitive decline (MESH:D003072), pulmonary hypertension (MESH:D006976), chronic diseases (MESH:D002908), aortic valve disease (MESH:D000082862), Frailty (MESH:D000073496), HCM (MESH:D000092183), tetralogy of Fallot (MESH:D013771), ventricular septal defect (MESH:D006345), compromised brain development (MESH:D002658), Function (MESH:D003291), hypertrophic cardiomyopathy (MESH:D002312), d-TGA (MESH:C538319), VSD (MESH:D004310), dementia (MESH:D003704), cardiac lesions (MESH:D006331), Ventricular dilation (MESH:C566255), TIA (MESH:D002546), arrhythmia (MESH:D001145), heart failure (MESH:D006333), slow gait speed (MESH:D020234), ASD (MESH:D001321), Eisenmenger (MESH:D004541), loss of weight and muscle mass (MESH:D015431), CHD (MESH:D006330), ventricular dysfunction (MESH:D018754), dilation (MESH:D002311), CVD (MESH:D002318), diabetes mellitus (MESH:D003920), weakness (MESH:D018908), Coarctation of the aorta (MESH:D001017), neurodevelopmental deficits and disabilities (MESH:D001289), cyanosis (MESH:D003490), brain injury (MESH:D001930), hypertension (MESH:D006973), compromised psychomotor speed and working memory (MESH:D011596), Pulmonary arterial hypertension (MESH:D000081029), TGA (MESH:D014188), atrial septal defect (MESH:D006344), AVSD (MESH:C562831), haemodynamic abnormalities (MESH:D000014)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946910/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946910/full.md

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Source: https://tomesphere.com/paper/PMC12946910