MarElia Catherine B, Kuehl Melanie N, Shemwell Tiffany A, Alman Amy C, Burkhardt Brant R
Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, 4202 East Fowler Avenue, Tampa, FL 33620, United States.
Department of Epidemiology and Biostatistics, College of Public Health, University of South Florida, Tampa, FL 33612, United States.
J Clin Transl Endocrinol. 2018 Feb 23;11:26-30. doi: 10.1016/j.jcte.2018.02.003. eCollection 2018 Mar.
PANcreatic-DERived factor (PANDER, FAM3B) is a novel hormone that regulates glucose levels via interaction with both the endocrine pancreas and liver. Prior studies examining PANDER were primarily conducted in murine models or but little is known regarding the circulating concentration of PANDER in humans, especially with regard to the association of type 2 diabetes (T2D) or overall glycemic regulation. To address this limitation, we performed a cross-sectional analysis of circulating serum PANDER concentration in association with other hormones that serve as either markers of insulin resistance (insulin and adiponectin) or to metabolic parameters of glycemic control such as fasting HbA1c and blood glucose (FBG).
Fasting serum was obtained from a commercial biorepository from 300 de-identified adult subjects with 150 T2D and non-T2D adult subjects collected from a population within the United States, respectively, matched on gender, age group and race/ethnicity. Concentration of PANDER, insulin and adiponectin were measured for all samples as determined by commercial ELISA. Metadata was provided for each subject including demography, anthropometry, and cigarette and alcohol use. In addition, fasting blood glucose (FBG) and HbA1c were available on T2D subjects.
Multiple linear regression analyses were performed to examine the relationships between circulating log PANDER concentration on HbA1c, fasting glucose, log insulin, log HOMA-β and log HOMA-IR among T2D subjects and for insulin and adiponectin in non-T2D subjects. A significant linear association was identified between PANDER with fasting HbA1c (β 0.832 ± SE 0.22, p = 0.0003) and FBG (β 20.66 ± SE 7.43, p = 0.006) within T2D subjects. However, insulin, HOMA-β, HOMA-IR and adiponectin (p > 0.05) were not found to be linearly associated with PANDER concentration.
Within T2D subjects, PANDER is modestly linearly associated with increased HbA1c and FBG in a US population. In addition, highest circulating PANDER levels were measured in T2D subjects with HbA1c above 9.9. No association was identified with PANDER and insulin resistance or pancreatic β-cell function in T2D subjects.
胰腺衍生因子(PANDER,FAM3B)是一种新型激素,通过与内分泌胰腺和肝脏相互作用来调节血糖水平。先前关于PANDER的研究主要在小鼠模型中进行, 但对于PANDER在人类中的循环浓度知之甚少,尤其是关于2型糖尿病(T2D)或整体血糖调节的关联。为了解决这一局限性,我们对循环血清中PANDER浓度与其他激素进行了横断面分析,这些激素可作为胰岛素抵抗标志物(胰岛素和脂联素)或血糖控制的代谢参数,如空腹糖化血红蛋白(HbA1c)和血糖(FBG)。
从一个商业生物样本库中获取空腹血清,该样本库来自300名身份不明的成年受试者,其中150名T2D成年受试者和非T2D成年受试者分别从美国的人群中收集,在性别、年龄组和种族/民族方面进行了匹配。通过商业酶联免疫吸附测定(ELISA)法测定所有样本中PANDER、胰岛素和脂联素的浓度。为每个受试者提供了元数据,包括人口统计学、人体测量学以及吸烟和饮酒情况。此外,T2D受试者可获得空腹血糖(FBG)和HbA1c数据。
进行了多元线性回归分析,以检验T2D受试者中循环logPANDER浓度与HbA1c、空腹血糖、log胰岛素、logHOMA-β和logHOMA-IR之间的关系,以及非T2D受试者中胰岛素和脂联素之间的关系。在T2D受试者中,发现PANDER与空腹HbA1c(β 0.832±标准误0.22,p = 0.0003)和FBG(β 20.66±标准误7.43,p = 0.006)之间存在显著的线性关联。然而,未发现胰岛素、HOMA-β、HOMA-IR和脂联素(p>0.05)与PANDER浓度呈线性相关。
在T2D受试者中,在美国人群中PANDER与HbA1c升高和FBG呈适度线性相关。此外,在HbA1c高于9.9的T2D受试者中检测到最高的循环PANDER水平。在T2D受试者中未发现PANDER与胰岛素抵抗或胰腺β细胞功能有关联。