Clinical Observation on Bone Metabolism Induced by Chronic Renal Insufficiency

Sponsor
Shanghai University of Traditional Chinese Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT02147782
Collaborator
Anhui Provincial Hospital (Other), Huadong Hospital (Other), Longhua Hospital (Other)
300
4
122
75
0.6

Study Details

Study Description

Brief Summary

Patients with chronic renal insufficiency usually develop secondary osteoporosis or bone loss, which is called renal osteodystrophy. Most of the previous studies focused on bone metabolism of patients in late stage of chronic renal insufficiency, especially those with chronic dialysis. In this study, bone metabolism of patients in different stages of chronic renal insufficiency will be observed to reveal the mechanism of development of renal osteodystrophy and provide clues for early intervention on renal osteodystrophy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    In this study, patients with chronic renal insufficiency (CKD1-5, defined by glomerular filtration rate,GFR) and healthy people as control will be recruited (50/group, total 300). Blood urea nitrogen, creatinine,lumbar and hip bone mineral density, bone turnover biochemical markers including serum total propeptide of type I procollagen(PINP), bone alkaline phosphatase(BALP), bone Gla-protein (BGP) and β-CrOSSlaps(β-CTX), serum calcium and phosphorus and related regulators including fibroblast growth factor 23 (FGF23), 25-hydroxyl-Vitamin D (25-OH-VitD), parathyroid hormone(PTH) will be detected. The relationship between kidney function and bone turnover, and the rules throughout the development process of renal osteodystrophy will be analysed.The micro ribonucleotide(miRNA)array will also be performed to screen the biomarkers of renal osteodystrophy in different stage.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Continuous Clinical Observation on Bone Metabolism Induced by Chronic Renal Insufficiency in Different Stages
    Actual Study Start Date :
    Oct 1, 2012
    Anticipated Primary Completion Date :
    Dec 1, 2022
    Anticipated Study Completion Date :
    Dec 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    control

    Healthy people from physical examination centers are recruited as controls.

    CKD1

    with clinical one or more symptoms and signs of kidney injury listed as below: Urinary albumin ( urinary albumin excretion rate≥30 mg/24 h.albumin-creatinine ratio≥3mg/mmol) urinary sediments abnormality renal tubular lesions renal histological abnormalities abnormal structure showed by imaging history of renal transplantation GFR≥90(ml/min/1.73m²)

    CKD2

    with clinical symptoms and signs of kidney injury, and 60<=GFR<=89(ml/min/1.73m²)

    CKD3

    with clinical symptoms and signs of kidney injury, and 30<=GFR<=59(ml/min/1.73m²)

    CKD4

    with clinical symptoms and signs of kidney injury, and 15<=GFR<=29(ml/min/1.73m²)

    CKD5

    with clinical symptoms and signs of kidney injury, and GFR<15(ml/min/1.73m²)

    Outcome Measures

    Primary Outcome Measures

    1. bone metabolism (bone mineral density and serum bone turnover biomarkers) [1 day after enrollment]

      lumbar (L1-4 as well as total) and hip (neck, troch, inter and word's) bone mineral density will be recorded by dual energy X-ray absorptiometry. Serum bone turnover biomarkers including total PINP, BGP, BALP and β-CTx will be detected.

    Secondary Outcome Measures

    1. Kidney function (blood creatinine and urea nitrogen,glomerular filtration rate) [1 day after enrollment]

      CKD1-5 will be graded by glomerular filtration rate,and blood creatinine and urea nitrogen will be detected.

    2. Calcium and phosphorus metabolism (serum calcium and phosphorus,calcium-phosphorus product, FGF23, PTH and 25-OH-VitD) [1 day after enrollment]

      Serum calcium and phosphorus will be detected and the calcium-phosphorus product will be calculated.Factors which are related with calcium and phosphorus including FGF23, PTH and 25-OH-VitD will be detected.

    3. MicroRNA array [1 day after enrollment]

      Blood plasma will be collected for microRNA array analysis to find specific biomarkers for each stage.We will also try to find biomarkers for better definitions of chronic renal insufficiency and renal osteodystrophy.

    Other Outcome Measures

    1. Baseline information (height, weight, sex) [1 day after enrollment]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    1. 20-50 years old

    2. chronic renal insufficiency (Control: normal kidney function; Case: CKD 1-5)

    3. be willing to and be able to join in the study and signed informed consent

    4. have not accepted systematical treatment on bone loss or osteoporosis

    Exclusion Criteria:
    1. allergies

    2. secondary osteoporosis caused by other diseases.

    3. postmenopausal women

    4. mental illness or psychosis

    5. patients with bone fracture and need surgery treatment

    6. taking any medicine that will affect bone metabolism for a long time and can not stop

    7. women during pregnant stage and breast-feed stage

    8. with deformity or disability

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Anhui Province Hospital of TCM Hefei Anhui China 230031
    2 Jiangsu Province Hospital of TCM Nanjing Jiangsu China
    3 Longhua hospital affiliated to Shanghai University of TCM Shanghai Shanghai China 200032
    4 Huadong Hospital Affiliated to Fudan University Shanghai Shanghai China 200040

    Sponsors and Collaborators

    • Shanghai University of Traditional Chinese Medicine
    • Anhui Provincial Hospital
    • Huadong Hospital
    • Longhua Hospital

    Investigators

    • Principal Investigator: Yongjun Wang, Doctor, Shanhgai University of TCM

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Bing Shu, Associate Professor, Shanghai University of Traditional Chinese Medicine
    ClinicalTrials.gov Identifier:
    NCT02147782
    Other Study ID Numbers:
    • Renal Osteodystrophy
    • 1RT1270,2010CB530400
    First Posted:
    May 28, 2014
    Last Update Posted:
    Sep 23, 2021
    Last Verified:
    Sep 1, 2021
    Keywords provided by Bing Shu, Associate Professor, Shanghai University of Traditional Chinese Medicine
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 23, 2021