Mediating Role of Myokines in the Dialogue Between Muscle and Bone Tissue in a Population of Healthy Women Aged 20-89 Years

Официальное название

Analysis of the Mediating Role of Myokines in the Dialogue Between Muscle and Bone Tissue in a Population of Healthy Women Aged 20-89 Years

Обзор

The main hypothesis is that muscle acts on bone tissue via the secretion of myokines (myostatin, follistatin, irisin). This is based on previous results showing that muscle mass in different patient populations with very different body mass indexes (anorexic or obese patients) is significantly and independently associated with bone mineral density.

Подробное описание

Bone densitometry using X-ray absorptiometry (DXA) is the reference technique for measuring Bone Mineral Density (BMD). According to the International Osteoporosis Foundation (IOF), if a single site is to be preferred, it should be the total hip or femoral neck, using a single NHANES III reference curve. It should be stressed, however, that this curve was obtained from a North American population with anthropometric parameters, notably body mass index (BMI), that differ from those of the European population, particularly the Caucasian population. Apparently, only one reference curve has been obtained in France, from the OFELY study in 1993. Given the age of this cohort and the possibility of BMI changes over time in the Caucasian population, but even more so, the impossibility of transposing this curve onto new DXAs of different brands, new reference curves need to be developed. DMS IMAGING is therefore financing the MONIKA study, with the CHU de Nîmes as sponsor.

As part of this study, some 425 healthy female volunteers aged between 20 and 89 will be recruited from three centers (Nîmes, Montpellier, Lyon). A DXA examination at various bone sites (femur, rachis, radius and whole body) will provide up-to-date normalcy curves for BMD, but also for body composition (fat and lean mass), which are currently lacking. Access to this population could also enable us to better understand bone physiology and the links that may exist between bone tissue and muscle and fat tissue.For example, the serum concentration of leptin, a hormone secreted by adipose tissue, is associated with bone mass in non-obese women.More recent data show that skeletal muscle also has a secretory activity, characterized by the production of myokines.In humans, there are various arguments in favour of myostatin's action on bone tissue.However, clinical studies in humans are very limited.Through two clinical studies, myokine levels were assessed in two populations with very different BMIs. Female patients suffering from anorexia nervosa, for example, showed decreased myostatin levels, increased follistatin levels and comparable irisin levels, in parallel with very low BMD, compared with a population of young, non-malignant women.

In obese women with high BMD, it was also shown that myostatin and follistatin levels were high, whereas irisin levels were lower than in a control population. Furthermore, the effect of lean body mass on BMD was partially mediated by irisin. These results are still preliminary, having been obtained on a small group of subjects, and merit further investigation on a representative population scale. However, there are apparently no age-dependent reference values for these myokines.

In addition to the involvement of these myokines in the muscle-bone complex, these factors could also be involved in the muscle-fat complex, since new functions are now being attributed to them, such as lipolysis, which could affect the concentrations of certain adipokines, such as leptin, which in turn could have an impact on bone formation and resorption. The main hypothesis is that muscle acts on bone tissue via the secretion of myokines (myostatin, follistatin, irisin). This is based on previous results showing that muscle mass in different patient populations with very different BMIs (anorexic or obese patients) is significantly and independently associated with BMD.

Вмешательства

• Диагностический тест Blood sample
  36 ml of blood in 3 x 7 ml dry tubes, 1 x 5 ml EDTA tube, 1 x 5 ml heparinized tube, 1 x 5 ml anti-protease tube)
• Диагностический тест Saliva sample
  5 ml of saliva will be taken.
• Диагностический тест Grip test
  The grip strength of the dominant arm will be measured with the participant in a standing position, with the arm close to the body and the elbow at 90◦ flexion, while the non-dominant arm will be positioned alongside the body. Three measurements will be taken for the dominant hand, and the mean value will be calculated and used for analysis. One minute is allowed between each repetition, to avoid muscle fatigue. Dynamometer quality control is ensured by regularly checking known resistance values
• Другое MicroFET2® maximum isometric force test
  The microFET2 device is used to test isometric force. The microFET2 dynamometer is battery-powered and ergonomically designed to fit in the palm of the hand. The system is microprocessor-controlled to provide accurate, repeatable muscle force readings. The microFET Clinical software automatically performs calculations and validity tests, and allows graphs to be generated from the data, enabling reports of different patient tests to be compared
• Другое Maximum isometric knee extension bench test.
  The maximal isometric knee extension strength test on a specially-adapted strength bench consists in performing 3 maximal contractions with 1 minute's rest between each test.
• Другое The SPPB (Short Physical Performance Battery)
  Battery of tests comprising a balance test, a walking speed test and a chair-lift test
• Другое The 6-minute walking test.
  Muscular function will be determined by the 6-minute walk test to assess aerobic endurance. Participants will be asked to walk for 6 min as fast as possible on a shuttle track. The distance (m) covered in 6 min will be measured. Walking speed (m/s) will be calculated as the distance (m) covered in 6 min. A walking speed \<0.8 m/s has been defined as a low value.
• Другое Segmental impedancemetry examination.
  Segmental impedancemetry involves measuring body composition using the body's resistance to the passage of a low-intensity electric current. This test is harmless to the body.
• Другое Indirect calorimetry test.
  An Indirect calorimetry is the standard method for measuring energy expenditure at rest. It is based on the principle that the human body burns nutrients using O2 and producing CO2.
• Другое Fardellone's questionnaire
  Completion of a questionnaires on calcium intake (Fardellone)

Первичные конечные точки

• Myostatin [Срок оценки: Baseline]
• Follistatin [Срок оценки: Baseline]
• Irisin [Срок оценки: Baseline]
• Bone Mineral Density [Срок оценки: Baseline]
• Lean body mass [Срок оценки: Baseline]

Вторичные конечные точки (12)

• Leptin [Срок оценки: Baseline]
• Adiponecotin [Срок оценки: Baseline]
• Fat mass [Срок оценки: Baseline]
• Bone mineral density: impedencemetry [Срок оценки: Baseline]
• Grip test [Срок оценки: Baseline]
• Isometric force [Срок оценки: Baseline]
• Walking test [Срок оценки: Baseline]
• Short Physical Performance Battery : Balance test [Срок оценки: Baseline]
• Short Physical Performance Battery : Walking speed test [Срок оценки: Baseline]
• Short Physical Performance Battery : Chair lift test [Срок оценки: Baseline]
• Plasma concentration of osteocalcin, a bone remodelling marker. [Срок оценки: Baseline]
• Plasma concentration of serum cross-linked C-telopeptide of type I collagen (CTX), a bone remodelling marker. [Срок оценки: Baseline]

Критерии участия

Критерии включения

• Self-reported Caucasian ethnicity (Europe, Middle East, North Africa) only as there is a difference in BMD by ethnicity.
• Person affiliated with or benefiting from a social security scheme.
• Free, informed consent signed by the participant and the investigator (at the latest on the day of inclusion and before any examination required by the research).

Критерии исключения

• Fragility fracture defined as a spontaneous or low-kinetic fracture (≤ one fall from height).
• Early menopause (< 40 years), hysterectomy (complete < 40 years), primary amenorrhea (absence of menstruation before 15 years), current amenorrhea of more than 3 months without contraceptive if the patient is less than 40 years old.
• Patients on treatments: prolonged corticosteroid therapy > 3 months or > 1 g (cumulative dose).
• Immobilization of more than 3 months, less than 12 months old.
• Hip fracture in a first-degree relative.

Patients with any of the following pathologies affecting bone, muscle or adipose tissue:

• Inflammatory bowel disease (IBD: Crohn's disease, ulcerative colitis) and untreated celiac disease.
• Renal insufficiency on dialysis or patients with nephrology follow-up.
• Known hypercalciuria.
• Osteomalacia, rickets, osteogenesis imperfecta.
• Osteopathy (Paget's disease, osteopetrosis, etc.).
• Chronic inflammatory rheumatism.
• Hemopathy, neoplasia.
• Hepatic insufficiency or chronic hepatitis.
• Endocrinopathy: diabetes, dysthyroidism, hypogonadism, hypercorticism, untreated acromegaly.
• Anorexia nervosa.
• Hyperparathyroidism (even controlled).
• History of digestive surgery (bariatric, gastrectomy, digestive resection other than appendectomy, etc.).
• History of organ transplantation.
• Chronic infectious disease (HIV, etc.).
• Weight loss of more than 10 kg within 6 months.
• Paresis, marked lameness or unloading of a limb, or prolonged immobilization of more than one month in the last 12 months.
• Patients on treatments that may affect bone mass or body composition:
• Biphosphonates (Alendronate (Fosamax® and generics), Risedronate (Actonel® and generics), Zoledronate (Aclasta® and generics).
• Teriparatide (Forsteo®).
• Denosumab (Prolia®)
• Selective estrogen receptor modulators (Clomifene, Tamoxifene, Toremifene, Raloxifene).
• Anabolic steroids.
• Strontium ranelate.
• Carbamazepine.
• Phenobarbital.
• Immunosuppressants.
• Patients on anti-epileptics.
• Patients with any of the following abnormalities in the measurement area:
• Major deformities of the wrist, hip or vertebrae.
• Compression of vertebral bodies, cementoplasty.
• Prosthesis, implant (breast, buttock, etc.), foreign body.
• Hip paraosteoarthropathy.
• Injection of radiological contrast medium, barium enema, nuclear medicine examination within 10 days.
• Intensive sport (more than 10 h/week).
• Extreme BMI (BMI < 18, BMI > 35 kg/m²).
• Loss of autonomy.
• People with neurodegenerative disorders affecting their ability to give consent.
• Pregnant, parturient or breast-feeding women.
• Participation in an interventional study involving a drug or medical device or a category 1 RIPH within 3 months prior to inclusion.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Фундаментальное исследование

Центры проведения

Франция · 2 центра

• C.H.R.U. Lapeyronie — Montpellier
• Chu Nimes — Nîmes

Идентификаторы

NCT: NCT06683222 · AO12022/2023/VB-01

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗