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Study on pathogenesis mechanisms of osteoporosis using multi-omics high-throughput sequencing

Study on pathogenesis mechanisms of osteoporosis using multi-omics high-throughput sequencing

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-BON-17011196
Enrollment
Unknown
Registered
2017-04-20
Start date
2017-04-13
Completion date
Unknown
Last updated
2017-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporosis

Interventions

Osteoporosis group:Collect patient samples
Control group:Collect healthy participant samples

Sponsors

People's Hospital of Deyang City
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: According to WHO standards, femoral neck or lumbar vertebrae bone density T =-2.5, the diagnosis of osteoporosis, T =-1 normal bone mass. Individuals included in the study had no history of drugs that might affect bone metabolism: glucocorticoids, estrogens, thyroid hormones, parathyroid hormone, fluoride, calcitonin, thiazide, barbiturate, Antiepileptic drugs, vitamin D and calcium preparations.

Exclusion criteria

Exclusion criteria: Previously suffering from bone metabolism diseases such as kidney disease, liver disease, thyroid disease, diabetes, hyperprolactinemia, ovariectomy, rheumatoid arthritis, ankylosing spondylitis, chronic abdominal bones and other adverse symptoms, Blood disease, and individuals who have undergone pathological fractures or traumatic fractures in the last year. Patients with hypertension, coronary atherosclerosis, myocardial infarction, cerebral infarction, and infectious disease were excluded from the study.

Design outcomes

Primary

MeasureTime frame
Methylation chip detection;mRNA sequencing;

Countries

China

Contacts

Public ContactYuehong Liu

People's Hospital of Deyang City

dyliuyh123@163.com+86 0838-2418112

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026