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Ultrasound to Assess Sarcopenia in Prader Willi Syndrome

Completed
Conditions
Prader-Willi Syndrome
Sarcopenia
Metabolic Syndrome
Interventions
Diagnostic Test: Ultrasound assessment of the right lower extremity muscles
Diagnostic Test: Dual-energy X-ray absorptiometry (DXA) scan
Registration Number
NCT06448871
Lead Sponsor
Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation
Brief Summary

The aim of the study is to examine the clinical applicability of ultrasound as a diagnostic tool for sarcopenia in individuals with PWS by investigating the association between ultrasound-derived measurements, DXA-derived measurements, and sarcopenia-related outcomes.

Detailed Description

Sarcopenia is an age-related loss of muscle mass plus low muscle strength, and/or low physical performance, that may affect over 25% of individuals over the age of 60, resulting in an increased likelihood of developing disability. Abnormal body composition with an increased in body fat mass and a decreased in skeletal muscle mass were noted in individuals with Prader Willi syndrome (PWS), thought to be related to hormonal deficiencies due to hypothalamic dysfunction, presenting as a unique congenital model of sarcopenia.

Muscle mass can be measured by dual-energy X-ray absorptiometry (DXA) scan device, but it is expensive, increased radiation exposure, and not easily accessible in all clinical practice. Ultrasound (USD) is a non-invasive, without ionising radiation, low-cost, and easily accessible tool for the assessment of soft tissue. There were increasing evidence for the use of USD in the measurement of muscle thickness (MT), cross-sectional area (CSA) and pennate anle (PA) of different muscle groups in different populations. However, the use of USD as a routine diagnostic tool in individuals with PWS has not been reported yet.

The aim of the study is to examine the clinical applicability of ultrasound as a diagnostic tool for sarcopenia in individuals with PWS by investigating the association between ultrasound-derived measurements, DXA-derived measurements, and sarcopenia-related outcomes.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria
  • Genetically diagnosed individuals with PWS who can cooperate with the examinations
Exclusion Criteria
  • Individuals with PWS who have arthritis, fractures, or severe musculoskeletal deformities that could interfere with the examinations.
  • Individuals with PWS who have severe cognitive impairment and are unable to read or sign the written consent.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
group 1, pws groupDual-energy X-ray absorptiometry (DXA) scanIndividuals with PWS, aged 7 to 65 years, and able to follow simple instructions in chinese language.
group 1, pws groupUltrasound assessment of the right lower extremity musclesIndividuals with PWS, aged 7 to 65 years, and able to follow simple instructions in chinese language.
Primary Outcome Measures
NameTimeMethod
DXA: skeletal muscle (SM)1 day

Lean index of skeletal muscle (SM) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA

DXA: body fat mass (BFM)1 day

Adipose index of body fat mass (BFM) using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA.

DXA: appendicular skeletal muscle mass index (ASMI)1 day

Lean index of appendicular skeletal muscle mass index (ASMI) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA

DXA: fat mass index (FMI)1 day

Adipose index of fat mass index using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA.

Muscle thickness ultrasound1 day

Ultrasound scanning of the muscle thickness of rectus femoris (RF), vastus lateralis (VL), and gastrocnemius medialis (GM) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer.

Pennation angle ultrasound1 day

Ultrasound scanning of the pennation angles of vastus lateralis (VL) and gastrocnemius medialis (GM) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer.

DXA: total lean body mass1 day

Lean index of total lean body mass (LBM) with Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA

DXA: percentage fat mass1 day

Adipose index of percentage fat mass using Hologic QDR-4500A, Hologic, Inc., Waltham, MA, USA.

Cross-sectional area ultrasound1 day

Ultrasound scanning of the cross sectional area of rectus femoris (RF) using B-mode ultrasonography (LOGIQ S8, GE Healthcare, USA) and a 7-15 MHz linear array transducer.

Secondary Outcome Measures
NameTimeMethod
Handgrip and lateral pinch strength1 day

Grip strength and lateral pinch will be assessed bilaterally using an isometric Baseline hydraulic hand dynamometer and pinch gauge.

Physical performance test: five-time chair stand test1 day

In the 5-time chair stand test participants perform five sit-to-stand movements as quickly as possible

Physical performance test: SPPB1 day

The short physical performance battery (SPPB) will be used, which measures balance, walking speed, strength, and endurance in the lower limbs, and is scored from zero to 12 (worst to best score).

Physical performance test: gait speed1 day

In the gait speed test participants walk over a 4-meter distance at their normal pace.

Trial Locations

Locations (1)

Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

🇨🇳

New Taipei City, Taiwan

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