Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study

Author:

Edouard Thomas1ORCID,Picot Marie-Christine2,Bajanca Fernanda3,Huguet Helena2,Guitarte Aitor3,Langeois Maud3,Chesneau Bertrand3,Kien Philippe Khau Van4,Garrigue Eric3,Dulac Yves3,Amedro Pascal5

Affiliation:

1. Hospital Purpan: Hopital Purpan

2. CHU Montpellier: Centre Hospitalier Universitaire de Montpellier

3. CHU Toulouse: Centre Hospitalier Universitaire de Toulouse

4. CHU Nimes: Centre Hospitalier Universitaire de Nimes

5. CHU de Bordeaux: Centre Hospitalier Universitaire de Bordeaux

Abstract

Abstract Background This cross-sectional controlled study aims to assess health-related quality of life (HRQoL) of children and adolescents with a molecular diagnosis of Marfan syndrome (MFS) or related disorders and to evaluate the factors associated with HRQoL in this population. Sixty-three children with MFS and 124 age- and sex-matched healthy children were recruited. HRQoL was assessed using the Pediatric Quality of Life Inventory (PedsQL™) generic questionnaire. The correlation between HRQoL scores and the different continuous parameters (age, body mass index, disease severity, systemic score, aortic sinus diameter, and aerobic physical capacity) was evaluated using Pearson’s or Spearman’s coefficient. A multiple linear regression analysis was performed on the two health summary self-reported PedsQL™ scores (physical and psychosocial) to identify the factors associated with HRQoL in the MFS group. Results Except for emotional functioning, all other domains of HRQoL (psychosocial and physical health, social and school functions) were significantly lower in children with MFS compared to matched healthy children. In the MFS group, the physical health summary score was significantly lower in female than in male patients (self-report, P = 0.04; proxy-report: P = 0.05) and also negatively correlated with the systemic score (self-report: P = 0.06; proxy-report: P = 0.03) and with the height Z-score (proxy-report: P = 0.03). There was no significant difference in the physical health summary scores between the different genetic subgroups. In the subgroup of 27 patients who performed a cardiopulmonary exercise test, self- and proxy-reported physical health summary scores were highly correlated with their aerobic physical capacity assessed by peak oxygen consumption (VO2max) and ventilatory anaerobic threshold (VAT). In the multivariate analysis, the most important independent predictors of decreased physical health were increased height, decreased body mass index, decreased VAT and use of prophylactic therapy. Conclusions This study reports an impaired HRQoL in children and adolescents with MFS or related conditions, in comparison with matched healthy children. Educational and rehabilitation programs must be developed and evaluated to improve exercise capacity and HRQoL in these patients. Trial registration: ClinicalTrials.gov, NCT03236571. Registered 28 July 2017, https://www.clinicaltrials.gov/study/NCT03236571

Publisher

Research Square Platform LLC

Reference45 articles.

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4. Loeys-Dietz Syndrome;Velchev JD;Adv Exp Med Biol,2021

5. Hiratzka LF, Bakris GL, Beckman JA, Bersin RM, Carr VF, Casey DE Jr, Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. Circulation. 2010;121(13):e266–369. 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of.

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