Landgraf Kathrin, Rockstroh Denise, Wagner Isabel V, Weise Sebastian, Tauscher Roy, Schwartze Julian T, Löffler Dennis, Bühligen Ulf, Wojan Magdalena, Till Holger, Kratzsch Jürgen, Kiess Wieland, Blüher Matthias, Körner Antje
Center for Pediatric Research Leipzig, Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany Integrated Research and Treatment Center IFB Adiposity Diseases, University of Leipzig, Leipzig, Germany.
Center for Pediatric Research Leipzig, Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany.
Diabetes. 2015 Apr;64(4):1249-61. doi: 10.2337/db14-0744. Epub 2014 Nov 12.
Accumulation of fat mass in obesity may result from hypertrophy and/or hyperplasia and is frequently associated with adipose tissue (AT) dysfunction in adults. Here we assessed early alterations in AT biology and function by comprehensive experimental and clinical characterization of 171 AT samples from lean and obese children aged 0 to 18 years. We show an increase in adipocyte size and number in obese compared with lean children beginning in early childhood. These alterations in AT composition in obese children were accompanied by decreased basal lipolytic activity and significantly enhanced stromal vascular cell proliferation in vitro, potentially underlying the hypertrophy and hyperplasia seen in obese children, respectively. Furthermore, macrophage infiltration, including the formation of crown-like structures, was increased in AT of obese children from 6 years on and was associated with higher hs-CRP serum levels. Clinically, adipocyte hypertrophy was not only associated with leptin serum levels but was highly and independently correlated with HOMA-IR as a marker of insulin resistance in children. In summary, we show that adipocyte hypertrophy is linked to increased inflammation in AT in obese children, thereby providing evidence that obesity-associated AT dysfunction develops in early childhood and is related to insulin resistance.
肥胖症中脂肪量的积累可能源于肥大和/或增生,并且在成年人中常与脂肪组织(AT)功能障碍相关。在此,我们通过对171份来自0至18岁瘦儿童和肥胖儿童的脂肪组织样本进行全面的实验和临床特征分析,评估了脂肪组织生物学和功能的早期变化。我们发现,与瘦儿童相比,肥胖儿童从幼儿期开始脂肪细胞大小和数量增加。肥胖儿童脂肪组织组成的这些变化伴随着基础脂解活性降低以及体外基质血管细胞增殖显著增强,这可能分别是肥胖儿童中所见肥大和增生的潜在原因。此外,从6岁起,肥胖儿童脂肪组织中的巨噬细胞浸润(包括冠状结构的形成)增加,并且与较高的血清hs-CRP水平相关。临床上,脂肪细胞肥大不仅与血清瘦素水平相关,而且与作为儿童胰岛素抵抗标志物的HOMA-IR高度且独立相关。总之,我们表明脂肪细胞肥大与肥胖儿童脂肪组织中炎症增加有关,从而提供了证据表明肥胖相关的脂肪组织功能障碍在幼儿期就已出现,并且与胰岛素抵抗有关。