Catabolic to anabolic transition during nutritional rehabilitation of female adolescents with anorexia nervosa.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yael Levy-Shraga, Idit Ron, Adi Enoch-Levy, Rina Hemi, Hannah Kanety, Ido Wolf, Daniel Stein, Amir Tirosh, Tami Rubinek, Dalit Modan-Moses
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引用次数: 0

Abstract

Anorexia nervosa (AN) is associated with profound changes in glucose homeostasis, activity of the GH-IGF-1 axis, and adipose tissue, bone, and protein metabolism. We aimed to characterize the transition from a catabolic to anabolic state during the nutritional rehabilitation of female adolescent inpatients with AN. The study comprised 41 patients (aged 15.6 ± 1.6 yr). Blood samples were obtained at the time of admission and upon attainment of target weight. A subgroup of 18 patients also had blood samples obtained during the early refeeding period. Changes in body mass index (BMI) and BMI-SDS during hospitalization (5.1 ± 2.0 mo) were positively correlated with changes in markers of anabolism including IGF-1 (r = 0.424, P = 0.006), procollagen type I N-terminal propeptide (P1NP) (r = 0.375, P = 0.016), klotho (r = 0.468, P = 0.002), and alkaline phosphatase (ALP) (r = 0.051, P = 0.001) and were negatively correlated with the change in cortisol levels (r = -0.331, P = 0.035). Furthermore, changes in markers of anabolism were intercorrelated. IGF-1 increased consistently throughout the study period (P < 0.001); however, other variables showed a biphasic pattern. During the early refeeding period, there was a decrease in C-terminal telopeptides of type I collagen (CTX-1) (P < 0.001), uric acid (P < 0.001), cortisol (P = 0.056), fatty acid-binding protein 4 (FABP4) (P = 0.04), and klotho (P = 0.038) levels, whereas urea/creatinine ratio (UCR) (P = 0.045) increased. During the later phase, there was an increase in ALP (P = 0.039), insulin (P = 0.04), homeostatic model assessment for insulin resistance (HOMA-IR) (P = 0.06), and klotho levels (P = 0.02). In conclusion, the early refeeding period was characterized by a decrease in markers of catabolism, whereas the later phase was characterized by an increase in anabolic markers. We suggest that IGF-1, UCR, and klotho may be used as markers of reversal of catabolism and shift toward anabolism in patients with severe malnutrition.NEW & NOTEWORTHY We provide a comprehensive temporal characterization of changes in biochemical markers of glucose homeostasis, GH-IGF-1 axis activity, and adipose tissue, bone, and protein metabolism during refeeding of adolescents with anorexia nervosa. Although IGF-I levels increased continuously, other markers showed a biphasic pattern: an early decrease in catabolic markers, followed by an increase in anabolic markers later during hospitalization. IGF-1, urea/creatinine ratio, and klotho emerged as potential clinical biomarkers of catabolic to anabolic transition in patients with severe malnutrition.

神经性厌食症女性青少年营养康复过程中分解代谢向合成代谢的转变。
神经性厌食症(AN)与葡萄糖稳态、GH-IGF-1轴活性、脂肪组织、骨骼和蛋白质代谢的深刻变化有关。我们的目的是描述女性青少年AN住院患者营养康复期间从分解代谢状态到合成代谢状态的转变。41例患者(年龄15.6±1.6岁)。在入院时和达到目标体重时采集血样。亚组18例患者也在早期再喂养期间获得血液样本。住院期间(5.1±2.0个月)BMI和BMI- sds的变化与IGF-1 (r=0.424, p=0.006)、P1NP (r=0.375, p=0.016)、klotho (r=0.468, p=0.002)、碱性磷酸酶(r=0.051, p=0.001)等合成代谢指标的变化呈正相关,与皮质醇水平的变化呈负相关(r=-0.331, p=0.035)。此外,合成代谢标志物的变化是相互关联的。IGF-1在整个研究期间持续增加(p
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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