<p>Assessment of beta-cell function in type 1 diabetes (T1D) has important implications in both clinical and research settings. Studies demonstrating the extent to which puberty influences C-peptide levels are scarce. The aim of this study was to evaluate the influence of pubertal stage, along with age and body mass index (BMI), on multiple C-peptide measures at T1D diagnosis. This study included 275 consecutive children aged between 1 and 18 years with newly diagnosed T1D. Fasting, prandial, and area under the curve (AUC) C-peptide, estimated using fasting and prandial C-peptide levels, were analyzed. Generalized linear regression models were utilized. Median age at diagnosis was 7.9 (1.1–17.3) years, and mean BMI standard deviation score (SDS) was − 0.4 ± 1.4. Of the patients, 66% were prepubertal. Median fasting and prandial C-peptide levels at diagnosis were 0.26 (0.05–1.8) ng/mL and 0.43 (0.05–3) ng/mL, respectively. Fasting C-peptide was almost perfectly correlated with prandial C-peptide (r<sub>s</sub> = 0.80, <i>P</i> &lt; 0.001). Fasting, prandial, and AUC C-peptide were positively related with BMI SDS, age, and pubertal stage at diagnosis (<i>P</i> &lt; 0.001 for all). All the associations persisted when the variables were included as independent variables in regression models. <i>Conclusions</i>: Pubertal stage significantly and independently impacts C-peptide levels at T1D diagnosis along with body mass index and age. The adjustments demonstrating the extent to which puberty influences C-peptide levels in new-onset T1D are presented. Our observations underline the existence of distinct endotypes of T1D characterized by differing immunopathological courses.<Table Float="No" ID="Taba"> <tgroup cols="2"> <colspec align="left" colname="c1" colnum="1" /> <colspec align="left" colname="c2" colnum="2" /> <tbody> <row> <entry align="left" nameend="c2" namest="c1"> <p><b>What is Known:</b></p> </entry> </row> <row> <entry align="left" nameend="c2" namest="c1"> <p>• <i>Throughout the evaluation of beta-cell function at T1D diagnosis, it is essential to consider the factors influencing C-peptide levels.</i></p> </entry> </row> <row> <entry align="left" nameend="c2" namest="c1"> <p><b>What is New:</b></p> </entry> </row> <row> <entry align="left" nameend="c2" namest="c1"> <p>• <i>While age and BMI at diagnosis are associated with beta-cell function, our findings set the stage for a greater understanding of the disease process with additional findings regarding puberty, supporting the existence of endotypes of T1D.</i></p> </entry> </row> </tbody> </tgroup> </Table></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Pubertal stage significantly and independently impacts C-peptide levels at type 1 diabetes diagnosis along with body mass index and age

  • Emine Ayça Cimbek,
  • Nazım Ercüment Beyhun,
  • Gülay Karagüzel

摘要

Assessment of beta-cell function in type 1 diabetes (T1D) has important implications in both clinical and research settings. Studies demonstrating the extent to which puberty influences C-peptide levels are scarce. The aim of this study was to evaluate the influence of pubertal stage, along with age and body mass index (BMI), on multiple C-peptide measures at T1D diagnosis. This study included 275 consecutive children aged between 1 and 18 years with newly diagnosed T1D. Fasting, prandial, and area under the curve (AUC) C-peptide, estimated using fasting and prandial C-peptide levels, were analyzed. Generalized linear regression models were utilized. Median age at diagnosis was 7.9 (1.1–17.3) years, and mean BMI standard deviation score (SDS) was − 0.4 ± 1.4. Of the patients, 66% were prepubertal. Median fasting and prandial C-peptide levels at diagnosis were 0.26 (0.05–1.8) ng/mL and 0.43 (0.05–3) ng/mL, respectively. Fasting C-peptide was almost perfectly correlated with prandial C-peptide (rs = 0.80, P < 0.001). Fasting, prandial, and AUC C-peptide were positively related with BMI SDS, age, and pubertal stage at diagnosis (P < 0.001 for all). All the associations persisted when the variables were included as independent variables in regression models. Conclusions: Pubertal stage significantly and independently impacts C-peptide levels at T1D diagnosis along with body mass index and age. The adjustments demonstrating the extent to which puberty influences C-peptide levels in new-onset T1D are presented. Our observations underline the existence of distinct endotypes of T1D characterized by differing immunopathological courses.

What is Known:

Throughout the evaluation of beta-cell function at T1D diagnosis, it is essential to consider the factors influencing C-peptide levels.

What is New:

While age and BMI at diagnosis are associated with beta-cell function, our findings set the stage for a greater understanding of the disease process with additional findings regarding puberty, supporting the existence of endotypes of T1D.