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Sarcopenic Obesity: Estimation of Prevalence and Identification of Clinical and Biological Determinants in a Cohort of Adult Obese Patients and Longitudinal Follow-up (OBESAR-2)

U

University Hospital, Clermont-Ferrand

Status

Not yet enrolling

Conditions

Obesity and Overweight

Treatments

Other: Collection of fluid samples

Study type

Interventional

Funder types

Other

Identifiers

NCT06880432
RBHP 2024 BOIRIE

Details and patient eligibility

About

Context: Obesity, defined as excessive body fat, can lead to disability and loss of autonomy. If there is concomitant quantitative and qualitative muscle loss, sarcopenic obesity (SO) is suspected in this context. Although this clinical entity was defined several years ago, it is only very recently that precise assessment criteria have been established for screening and diagnosing this pathology (Donini et al. 2022).

Defined by the ESPEN/EASO consensus, SO has various consequences for health, particularly in terms of mobility and worsening of co-morbidities. It is therefore necessary to screen for SO, to determine its prevalence in the general population and to identify the determining factors in the loss of muscle mass during obesity. Most studies on the prevalence of sarcopenic obesity focus on the elderly population, bearing in mind that the prevalence of this syndrome in the elderly will increase rapidly as a result of the shift in the incidence of obesity from adults to this population in the coming decades.

The aim of this project is to determine the prevalence and determining or predisposing factors for sarcopenic obesity in a population of obese people in a broad age range (18-70 years).

Longitudinal follow-up of this cohort is planned in order to assess multifactorial changes (body composition, muscle function and physical performance) at 5 and 10 years after their inclusion in the OBESAR-2 study. In addition, patients who have undergone bariatric surgery will also be followed in the shorter term to analyse the phenotypic changes induced by rapid weight loss on muscle loss.

Enrollment

1,200 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Age: 18-70
  • Sex: men and women
  • Clinical nutrition patient receiving a metabolic assessment to optimise clinical and paraclinical management
  • Patient meeting obesity criteria defined by BMI > 30 kg/m².
  • Patient of legal age who has given free, informed and signed consent
  • Patient covered by social security

Non-inclusion criteria :

  • Patients with cancer or severe chronic disease (renal failure, respiratory failure, liver failure)
  • Patients with neuromuscular disease
  • Patient with total walking disability
  • Patients who are minors
  • Patient refusing to take part in the study
  • Pregnant or breast-feeding women
  • Under guardianship, curatorship, deprived of liberty or under court protection
  • Patient who has taken part in the OBESAR study

Trial design

Primary purpose

Screening

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,200 participants in 1 patient group

Cohort
Other group
Description:
Collection of clinical and paraclinical data (biological and anthropometric) for evaluation of sarcopenic obesity in obese patients.
Treatment:
Other: Collection of fluid samples

Trial contacts and locations

1

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Central trial contact

Lise Laclautre

Data sourced from clinicaltrials.gov

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