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Cushing's Osteoporosis Specificities

Completed
Conditions
Osteoporosis in Cushing's Syndrome
Osteoporosis in Post-menopausal Women
Interventions
Other: Osteodensitometry and pQCT
Registration Number
NCT03162068
Lead Sponsor
University Hospital, Clermont-Ferrand
Brief Summary

Osteoporosis induced by glucocorticoids excess constitutes the main cause of secondary osteoporosis. Most of data available are provided from cohort studies of patients treated by corticosteroids, affecting among 1% of population. In contrast, very few data on osteoporosis are available in the Cushing syndrome (CS), a rare disease affecting 1 or 2 million of inhabitants, and characterized by an endogen glucocorticoid excess production. This affection is responsable of frequent fractures, occuring in 30-60% of patients (vertebral asymptomatic in 50% of case, hip, ribs). Fractures occurs often frequently above the threshold usually used for osteoporosis (T-score\<-2.5), most often in the range of osteopenia. These data suggest that surface bone density isn't sufficient to characterize bone fragility, architectural factors are probably involved, and should be evaluated. The specificity of osteoporosis induced by endogen glucocorticoids excess in comparison with osteoporosis induced by estrogenic deficiency in post-menopausal women is poorly known, especially in endogen glucocorticoid excess.

A recent microarchitecture studies showed alterations of cortical compartment in patients with Cushing's syndrome, confirming by our preliminary preclinical data from a transgenic murin model of Cushing's syndrome.

In these ten last years, new radiologic tools have been developped, and are able to evaluate bone architecture. The peripheral Quantitative Computed analyses the bone architecture with distinction between cortical and trabecular compartment.

Therefore, we aim to determine the specificity of osteoporosis induced by glucocorticoids excess in comparison to post menopausal osteoporosis thanks to pQCT analysis.

Detailed Description

This study are divided in two parts :

- Cross sectional cohort with both comparison between : Cushing syndrome versus control and cushing syndrome versus post-menopausal women

Outcomes :

Primary outcomes : Analysis thanks to pQCT will be carried out in order to compare radius and tibia bone mineral volume (total, trabecular and cortical)

Secondary outcomes :

Strength parameters, muscle area adipose tissue surface will be assessed. Analysis of body composition thanks to DXA (Dual Energy X ray Absorptiometry), and surface bone mineral density.

Evaluation of Vertebral Fracture Assesment

- Prospective cohort with a longitudinal follow up on 5 years to assess the evolution of osteoporosis after treatment of Cushing syndrome (surgery or medical treatment).

CS patients are recruited during hospitalisation in endocrinology service Post-menopausal women are recruited within rheumatology service. Cases are recruited thanks to advertisement within CHU.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
50
Inclusion Criteria
  1. Cases

    • Healthy Volunteers
    • Men and women> 18 years
    • No known chronic treatment or pathology
    • Absence of tobacco or alcohol
    • Normal bone mineral density for age (Z-score> -2 and T-score> -2.5) and markers of bone remodeling in normal values for age and menopausal status (osteocalcin, CTX)
    • Free 24-hour urinary cortisol (CLU / 24 h) normal Cushing matching by menopausal status, age group, BMI, sex
  2. Postmenopausal women

    • Menopause confirmed by hormonal assays
    • Amenorrhea for more than one year
    • Free 24-hour urinary cortisol (CLU / 24 h) normal
    • Osteoporosis confirmed at DXA (T score ≤ -2.5 DS) Post menopausal women matching according to BMI, T-DXA score (T score ≤ -2.5 DS)
  3. Cushing's syndrome

    • Endogenous hypercorticism, whatever the cause (dependent or independent ACTH)
    • Active or controlled for less than 5 years
Exclusion Criteria
  1. Diseases with bone resonance:

    • Disease that can affect phosphocalcium metabolism or promote bone loss: endocrine diseases (hyperparathyroidism, hyperthyroidism); Osteomalacia, malabsorptive intestinal or inflammatory or chronic liver diseases, chronic inflammatory rheumatism.
    • Heavy comorbidities: heart failure or chronic respiratory insufficiency, known severe renal insufficiency.
  2. Treatments:

    • Anti-osteoporotic treatments (bisphosphonates, raloxifene, denosumab)
    • Teriparatide; Lithium, thiazide diuretic, treatment with levothyrox suppressive dose, hormone replacement therapy of menopause, anticonvulsants, corticotherapy in progress or in the previous 5 years, anti-aromatases, anti-androgenic
  3. Other:

    • Minors, pregnant women
    • Patients unable to express their will (sub-tutelage, curators, dementia).
    • Lack of social security
    • Lack of follow-up
    • Excessive consumption of alcohol

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Cushing' syndrome groupOsteodensitometry and pQCTCushing' syndrome patients are recruited during hospitalisation in endocrinology service
Post menopausal womenOsteodensitometry and pQCTPost-menopausal women are recruited within rheumatology service.
Control groupOsteodensitometry and pQCTCases are recruited thanks to advertisement within CHU.
Primary Outcome Measures
NameTimeMethod
Comparison of volumetric bone mineral densityat day 1

thanks to pQCT with evaluation of total, trabecular and cortical compartment, between patients affecting by cushing'syndrome and post-menopausal women

Secondary Outcome Measures
NameTimeMethod
Assessment of trabecular and cortical compartmentat day 1

comparison Cushing syndrome versus both menopause women and controls : pQCT analysis

Assessment of strength bone of radius and tibia of the non-dominant limbat day 1

comparison Cushing syndrome versus both menopause women and controls : pQCT analysis

Comparison of muscle area and surface, adipose tissueat day 1

comparison Cushing syndrome versus both menopause women and controls : pQCT analysis

Trial Locations

Locations (1)

CHU Clermont-Ferrand

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Clermont-Ferrand, Auvergne, France

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