In humans increase in intrapancreatic adipose tissue predicts beta-cell dedifferentiation score before diabetes onset: A pilot study.

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Tác giả: Sergio Alfieri, Adriana Avolio, Michela Brunetti, Umberto Capece, Gea Ciccarelli, Francesca Cinti, Saverio Cinti, Antonio Gasbarrini, Andrea Giaccari, Gianfranco Di Giuseppe, Shawn Gugliandolo, Teresa Mezza, Simona Moffa, Cassandra Morciano, Rossana Moroni, Enrico Celestino Nista, Alfredo Pontecorvi, Giuseppe Quero, Martina Senzacqua, Ilenia Severi, Laura Soldovieri, Vincenzo Tondolo

Ngôn ngữ: eng

Ký hiệu phân loại: 636.0885 Animal husbandry

Thông tin xuất bản: Ireland : Diabetes research and clinical practice , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 68372

 BACKGROUND: The role of intrapancreatic fat (WAT) in the development of T2D remains debated. In T2D, β-cell dedifferentiation is one of the mechanisms responsible for β-cell failure but its role in prediabetes is unknown. We aimed to investigate the relation between WAT and β-cell dedifferentiation prior to diabetes onset. METHODS: We evaluated pancreatic samples from patients without history of diabetes, who had previously undergone an oral glucose tolerance test and hyperglycemic clamp. Subjects were divided into 3 glucose tolerance groups: normal (NGT), altered (IGT) or newly diagnosed diabetes (nDM). Dedifferentiation and WAT% were morphologically assessed. RESULTS: WAT was higher in nDM patients compared to NGT and IGT (WAT nDM 43.79 ± 20.83 %, IGT 10.67 ± 8.5 %, NGT 4.43 ± 4.37 %). We observed a progressive increase in dedifferentiation score, in parallel with worsening glucose tolerance (from NGT to IGT to nDM
  4.8 ± 3.8
  32.37 ± 7.4
  40.38 ± 19 respectively). A strong linear regression established that WAT could statistically significantly predict dedifferentiated β-cells (R = 0.86, p = 0.005), and that the predicted increase in dedifferentiated β-cells was 1.25 points for every extra one-point change in WAT. Interestingly, the WAT and dedifferentiation score variable pair were significantly related to 1-hour post-load glycemia. CONCLUSIONS: The accumulation of WAT might be responsible for dedifferentiation, making it a potential new target to curb diabetes onset.
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