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Trial Title: Single-Cell Sequence Technology Used to Reveal Heterogeneity of Secondary Hyperparathyroidism

NCT ID: NCT06130683

Condition: Secondary Hyperparathyroidism

Conditions: Official terms:
Neoplasm Metastasis
Hyperparathyroidism
Hyperparathyroidism, Secondary

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Other
Intervention name: Single-cell sequencing
Description: Single-cell sequencing technology can reveal the gene structure and gene expression status of individual cells, reflecting the heterogeneity between cells.
Arm group label: Normal group
Arm group label: Primary Hyperparathyroidism
Arm group label: Secondary Hyperparathyroidism

Summary: This project intends to select cases that meet the research requirements, take secondary hyperparathyroidism, primary hyperparathyroidism and normal human parathyroid tissue, a total of three groups, 4 cases in each group, through the method of single-cell transcription and sequencing, construct a map of human parathyroid function types, reveal the gene structure and gene expression status of cells, and visualize the expression characteristics, intercellular heterogeneity, and heterogeneity of cell subsets of secondary hyperparathyroid cells in a hierarchical manner, draw a single-cell map, and compare the differences between groups. To explore the pathogenesis of secondary hyperparathyroidism. Secondary hyperparathyroidism, parathyroid tissue of primary hyperparathyroidism and normal parathyroid tissue obtained by accident were collected, frozen and preserved, frozen tissue thawed, single-cell suspension was prepared and each cell was specifically labeled by the Mozhuo Genomics system, after oil breaking, polymerase chain reaction amplification, reverse transcription to obtain complementary DNA, and a library of complementary DNA that passed quality inspection was constructed to obtain high-quality data of parathyroid cells. Cell Ranger, R Seurat package, and t-SNE dimensionality reduction diagram were used to reduce the dimensionality, cluster, and visualize the data. In order to construct a single-cell atlas of parathyroid glands, investigators performed cluster analysis of similar cells according to the gene expression profile, and then visualized the data by t-SNE. According to the results of cell clustering, the specific and highly expressed genes in each cell cluster were identified. Cell populations were identified according to the expression of landmark genes, and the differences in cell types and proportions between groups were compared.

Criteria for eligibility:

Study pop:
People who undertake surgery for secondary hyperparathyroidism or primary hyperparathyroidism and other neck surgeries in our China-Japan Friendship Hospital

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Study participants with a diagnosis of secondary hyperparathyroidism who underwent surgical treatment - Study participants with a diagnosis of primary hyperparathyroidism who underwent surgical treatment - Study participants who have obtained informed consent Exclusion Criteria: - Other non-secondary hyperparathyroidism conditions such as primary hyperparathyroidism were excluded at the time of inclusion of study participants with essential hyperparathyroidism. - Other non-primary hyperparathyroid conditions such as secondary hyperparathyroidism were excluded at the time of inclusion of study participants with essential hyperparathyroidism. - Refusal of informed consent.

Gender: All

Minimum age: 18 Years

Maximum age: 80 Years

Healthy volunteers: No

Locations:

Facility:
Name: China and Japan Friendship Hospital

Address:
City: Beijing
Country: China

Status: Recruiting

Contact:
Last name: Meng Yang

Phone: 13651107012
Email: mengyang7012@163.com

Start date: November 8, 2023

Completion date: July 31, 2025

Lead sponsor:
Agency: China-Japan Friendship Hospital
Agency class: Other

Source: China-Japan Friendship Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06130683

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