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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06351176
Other study ID # 2024-6819
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date July 4, 2023
Est. completion date August 29, 2025

Study information

Verified date April 2024
Source CHU de Quebec-Universite Laval
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Background : Type 1 diabetes (T1D) is associated with an increased risk of fractures. The mechanisms accounting for this bone fragility are not yet fully understood. As T1D is often diagnosed in childhood or early adulthood, the lower bone mineral density (BMD) and deteriorated bone microarchitecture observed in T1D may reflect changes in the bone that occurred before or at the time of peak bone mass achievement. There is a lack of high-quality prospective studies to determine whether adults with T1D continue to lose BMD or deteriorate bone quality compared with controls. Moreover, while chronic hyperglycemia is a risk factor for fracture in T1D, it is unknown if better glycemic control affects bone outcomes. This prospective multicenter cohort study aims: (1) To compare the changes in the following outcomes over 4 years in adults with T1D and controls without diabetes of similar age, sex and body-mass index distribution: BMD by dual-energy X-ray absorptiometry (DXA) at the femoral neck, hip, spine, and radius, trabecular bone score (TBS) by DXA, and serum biochemical markers of bone turnover (BTMs); (2) To evaluate whether long-term glycemic control or the presence of a microvascular complication are independent predictors of the changes in BMD and TBS in people with T1D.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 163
Est. completion date August 29, 2025
Est. primary completion date December 22, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years and older
Eligibility Individuals with type 1 diabetes who have participated in the DenSiFy (Diabetes Spine Fractures) study (NCT04064437) Inclusion Criteria: - Diagnosis of type 1 diabetes for at least 5 years; - Age 20 years and older. Exclusion Criteria: - Pregnancy, delivery or breastfeeding in the past 6 months; - Conditions associated with bone disease (significant liver disease, intestinal malabsorption other than celiac disease, organ transplant, active cancer, rheumatoid arthritis, hyperthyroidism, hypothyroidism with abnormal TSH, hyperparathyroidism, hypoparathyroidism, hypogonadism, acromegaly, Cushing syndrome, adrenal insufficiency); - Any of these medications since the first DenSiFy study visit : biphosphonates, teriparatide, denosumab, calcitonin, glucocorticoids = 7,5 mg prednisone/day or equivalency = 3 months, aromatase inhibitors, antiandrogens, antiepileptic drugs, anticoagulants, thiazolidinediones; - Inability to consent. Healthy controls who have participated in the DenSiFy (Diabetes Spine Fractures) study (NCT04064437) Inclusion Criteria: - Age 20 years and older. Exclusion Criteria : - As above (as individuals with diabetes), and : - Diagnosis of diabetes or prediabetes; - Celiac disease; - Chronic kidney disease (CrCl < 60 mL/min).

Study Design


Intervention

Diagnostic Test:
Clinical tests
The investigators perform the following clinical tests: vibration threshold test, monofilament test, and height, weight and waist circumference measurement in every participant.
Biochemical tests
The investigators perform blood and urine tests in every participant.
DXA scan with TBS and VFA
The investigators perform a dual energy x-ray absorptiometry (DXA scan or osteodensitometry) including trabecular bone score (TBS) and Vertebral Fracture Assessment (VFA) in every participant.
AGEReader
The investigators perform a skin advanced glycation end products (AGEs) measurement with the AGE Reader machine in every participant.

Locations

Country Name City State
Canada Institut de recherches cliniques de Montréal (IRCM) Montréal Quebec
Canada Centre de recherche du CHU de Québec-Université Laval Quebec City Quebec

Sponsors (2)

Lead Sponsor Collaborator
CHU de Quebec-Universite Laval Diabetes Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Areal bone mineral density at the femoral neck, g/cm2 Measured by DXA scan 4-year visit
Other Areal bone mineral density at the femoral neck, T-Score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the femoral neck, Z-Score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the total hip, g/cm2 Measured by DXA scan 4-year visit
Other Areal bone mineral density at the total hip, T-score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the total hip, Z-score Measured by DXA scan 4 year visit
Other Areal bone mineral density at the spine, g/cm2 Measured by DXA scan 4-year visit
Other Areal bone mineral density at the spine, T-Score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the spine, Z-score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the distal third of radius, g/cm2 Measured by DXA scan 4-year visit
Other Areal bone mineral density at the distal third of radius, T-score Measured by DXA scan 4-year visit
Other Areal bone mineral density at the distal third of radius, Z-score Measured by DXA scan 4-year visit
Other Trabecular bone score (TBS) at the lumbar spine (L1-L4) (unitless) TBS calculated with the software TBSinSight 4-year visit
Other Vertebral Fracture Assessment (VFA) from the T4 to L5 vertebrae to detect the presence of vertebral fracture Image acquired by DXA 4-year visit
Other Lean mass (arm, leg, trunk, android, gynoid and total) (g) Body composition measured by DXA scan 4-year visit
Other Fat mass (arm, leg, trunk, android, gynoid and total) (g) Body composition measured by DXA scan 4-year visit
Other C-terminal cross-linking telopeptide of type I collagen (C-telopeptide, CTX) (ng/mL) Bone turnover marker, bone resorption (serum) 4-year visit
Other Procollagen type 1 N-terminal propeptide (P1NP) (ng/mL) Bone turnover marker, bone formation (serum) 4-year visit
Other Osteocalcin (ng/mL) Bone turnover marker, bone formation (serum) 4-year visit
Other Sclerostin (pmol/mL) Inhibitor of bone formation (serum) 4-year visit
Other Change in C-terminal cross-linking telopeptide of type I collagen (C-telopeptide, CTX) (ng/mL) Bone turnover marker, bone resorption (serum) Between the baseline and the 4-year visit
Other Change in osteocalcin (ng/mL) Bone turnover marker, bone formation (serum) Between the baseline and the 4-year visit
Other Change in procollagen type 1 N-terminal propeptide (P1NP) (ng/mL) Bone turnover marker, bone formation (serum) Between the baseline and the 4-year visit
Other Change in sclerostin (pmol/mL) Inhibitor of bone formation (serum) Between the baseline and the 4-year visit
Other Skin advanced glycation end-products (AGEs) (arbitrary units) Measured with AGEReader (autofluorescence) 4-year visit
Other Glycated hemoglobin (HbA1c, %) Diabetes control marker 4-year visit
Other Fasting glucose (mmol/L) Blood level measurement 4-year visit
Other Complete blood count Blood level measurement 4-year visit
Other Thyroid-stimulating hormone (TSH) (mU/L) Blood level measurement 4-year visit
Other Lipid panel (total cholesterol, LDL-cholesterol, HDL-cholesterol, non-HDL-cholesterol, total cholesterol/HDL-cholesterol ratio, triglycerides, in mmol/L) Blood level measurement 4-year visit
Other Creatinine (umol/L) Blood level measurement 4-year visit
Other Microalbuminuria (mg/mmol) Urine microalbuminuria/ urine creatinine ratio measurement 4-year visit
Other Liver enzymes (AST, ALT) (U/L) Blood level measurement 4-year visit
Other Calcium (mmol/L) Blood level measurement 4-year visit
Other Albumine (g/L) Blood level measurement 4-year visit
Other Phosphate (mmol/L) Blood level measurement 4-year visit
Other 25-hydroxyvitamin D3 (nmol/L) Blood level measurement 4-year visit
Other Parathormone (PTH) (ng/L) Blood level measurement 4-year visit
Other Antitransglutaminase antibodies (U/mL) Blood level measurement 4-year visit
Other Immunoglobulin A (IgA) (g/L) Blood level measurement 4-year visit
Other Insulin like growth factor-1 (IGF-1) (ng/mL) Blood level measurement 4-year visit
Other Follicle stimulating hormone (FSH, women) (U/L) Blood level measurement 4-year visit
Other Total testosterone (men) (nmol/L) Blood level measurement 4-year visit
Other Sex hormone-binding globulin (SHBG, men) (nmol/L) Blood level measurement 4-year visit
Primary Change in areal bone mineral density (aBMD) at the femoral neck in g/cm2 aBMD measured by DXA scan Between the baseline and the 4-year visit
Secondary Change in areal bone mineral density (aBMD) at the spine in g/cm2 aBMD measured by DXA scan Between the baseline and the 4-year visit
Secondary Change in areal bone mineral density (aBMD) at the total hip in g/cm2 aBMD measured by DXA scan Between the baseline and the 4-year visit
Secondary Change in areal bone mineral density (aBMD) at the distal third of radius in g/cm2 aBMD measured by DXA scan Between the baseline and the 4-year visit
Secondary Change in Trabecular bone score (TBS) (unitless) TBS with the software TBSinSight Between the baseline and the 4-year visit
Secondary Glycemic control, assessed with mean glycated hemoglobin (HbA1c) of the past 7 years Mean HbA1c of the past 7 years from all the available HbA1c in the medical record 4-year visit
Secondary Glycemic control, assessed with skin advanced glycation end products (AGEs) Skin AGEs measured with AGEReader (autofluorescence) 4-year visit
Secondary Presence of a microvascular complication (neuropathy, nephropathy, retinopathy) From the information available in the medical record and from monofilament and vibration testing (for neuropathy) and from microalbuminuria (nephropathy) 4-year visit
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