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Article

Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis

  • Authors:
    • Min Yang
    • Changji Du
    • Yinping Wang
    • Jun Liu
  • View Affiliations / Copyright

    Affiliations: Department of Endocrinology, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200240, P.R. China, Department of Clinical Lab, The Daopei Hospital of Shanghai, Shanghai 200240, P.R. China
  • Pages: 4338-4345
    |
    Published online on: April 25, 2017
       https://doi.org/10.3892/mmr.2017.6507
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Abstract

Hashimoto's thyroiditis (HT) is characterized by dysregulated immune responses and is commonly associated with insulin resistance. However, the mechanism of insulin resistance in HT remains to be fully elucidated. The aim of the present study was to investigate the correlation between the percentage of B regulatory lymphocytes (Bregs) and insulin resistance in patients with HT but with normal thyroid function (type I). A total of 59 patients with type I HT and 38 healthy volunteers were enrolled in the study. An oral glucose tolerance test was performed to measure insulin secretion and assess β‑cell functions. Flow cytometry was performed to examine the percentages of lymphocyte populations. The patients with HT exhibited normal fasting and postprandial glucose and fasting insulin secretion, but increased secretion of early‑phase and total insulin. The patients with HT also had insufficient β‑cell compensation for insulin resistance, indicated by a reduced disposition index, in the fasting state. An elevation in the percentage of CD19+CD24+CD27+ Bregs was also observed, which correlated positively with insulin secretion and insulin resistance in the fasting state. The patients with type I HT had postprandial insulin resistance and insufficient β‑cell compensation for fasting insulin resistance. Therefore, the increase in CD19+CD24+CD27+ Bregs was closely associated with fasting insulin secretion. These results provide novel insight into the mechanism of insulin resistance in HT.
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Copy and paste a formatted citation
Spandidos Publications style
Yang M, Du C, Wang Y and Liu J: Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis. Mol Med Rep 15: 4338-4345, 2017.
APA
Yang, M., Du, C., Wang, Y., & Liu, J. (2017). Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis. Molecular Medicine Reports, 15, 4338-4345. https://doi.org/10.3892/mmr.2017.6507
MLA
Yang, M., Du, C., Wang, Y., Liu, J."Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis". Molecular Medicine Reports 15.6 (2017): 4338-4345.
Chicago
Yang, M., Du, C., Wang, Y., Liu, J."Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis". Molecular Medicine Reports 15, no. 6 (2017): 4338-4345. https://doi.org/10.3892/mmr.2017.6507
Copy and paste a formatted citation
x
Spandidos Publications style
Yang M, Du C, Wang Y and Liu J: Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis. Mol Med Rep 15: 4338-4345, 2017.
APA
Yang, M., Du, C., Wang, Y., & Liu, J. (2017). Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis. Molecular Medicine Reports, 15, 4338-4345. https://doi.org/10.3892/mmr.2017.6507
MLA
Yang, M., Du, C., Wang, Y., Liu, J."Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis". Molecular Medicine Reports 15.6 (2017): 4338-4345.
Chicago
Yang, M., Du, C., Wang, Y., Liu, J."Increased CD19+CD24+CD27+ B regulatory cells are associated with insulin resistance in patients with type I Hashimoto's thyroiditis". Molecular Medicine Reports 15, no. 6 (2017): 4338-4345. https://doi.org/10.3892/mmr.2017.6507
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