Neopterin, a Marker of Interferon-Gamma-Inducible Inflammation, Correlates with Pyridoxal-5'-Phosphate, Waist Circumference, HDL-Cholesterol, Insulin Resistance and Mortality Risk in Adult Boston Community Dwellers of Puerto Rican Origin.

G Oxenkrug, K L Tucker, P Requintina, P Summergrad
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引用次数: 43

Abstract

Interferon-gamma (IFNG), a pro-inflammatory cytokine, increases concentrations of neopterin, a stable pteridine derivative, due to IFNG-induced transcriptional activation of the rate-limiting enzyme of pteridines biosynthesis. Neopterin concentrations were reported to correlate with metabolic syndrome (MetS), the cause of increased mortality risk, in subjects of European ancestry. We were interested to assessed neopterin correlations with clinical markers of MetS and mortality risk in population with a different genetic background, i.e., Puerto Ricans residents of Boston. Since inflammation is associated with pyridoxal-5'-phosphate (PLP) deficiency, we assessed correlations of neopterin with PLP. Plasma neopterin concentrations were evaluated in 592 adult (45-75 years of age) participants of Boston Puerto Rican Health Study. Neopterin concentrations correlated with abdominal obesity (waist circumference, r = 0.085, p < 0.038), HDL cholesterol (r = -0.15, p < 0.0001), insulin resistance (HOMA-IR, r = 0.08, P < 0.03), and plasma pyridoxal-5'-phosphate (PLP (r = -0.13, P = 0.002). Neopterin concentrations of >16 nmol/L at baseline were associated with the increased risk of mortality in 113 subjects followed for 6 years. The present results together with previously reported data in European subjects suggest a similar pattern of neopterin correlations with MetS and mortality risk in population with different genetic backgrounds. PLP is a cofactor of IFNG-induced key enzymes of tryptophan-kynurenine metabolism. Since PLP deficiency is associated with the increased production of diabetogenic kynurenine derivative, xanthurenic acid, our results suggest that up-regulated IFNG production might contribute to the development of insulin resistance. Assessment of neopterin concentrations might help to monitor the activity of IFNG-inducible inflammation associated with aging-associated medical and psychiatric disorders.

在波多黎各裔波士顿社区居民中,干扰素- γ诱导炎症的标记物Neopterin与吡多醛-5'-磷酸、腰围、高密度脂蛋白胆固醇、胰岛素抵抗和死亡风险相关。
干扰素- γ (IFNG)是一种促炎细胞因子,由于IFNG诱导了蝶啶生物合成限速酶的转录激活,从而增加了新蝶呤(一种稳定的蝶啶衍生物)的浓度。据报道,在欧洲血统的受试者中,新蝶呤浓度与代谢综合征(MetS)相关,这是导致死亡风险增加的原因。我们有兴趣评估新蝶呤与具有不同遗传背景的人群(即波士顿的波多黎各居民)中met临床标志物和死亡风险的相关性。由于炎症与吡哆醛-5'-磷酸(PLP)缺乏有关,我们评估了新蝶呤与PLP的相关性。对592名波士顿波多黎各健康研究参与者(45-75岁)的血浆新蝶呤浓度进行了评估。新蝶呤浓度与腹部肥胖(腰围,r = 0.085, p < 0.038)、高密度脂蛋白胆固醇(r = -0.15, p < 0.0001)、胰岛素抵抗(HOMA-IR, r = 0.08, p < 0.03)、血浆吡多醛-5′-磷酸(PLP) (r = -0.13, p = 0.002)相关。113名受试者随访6年,基线时新蝶呤浓度>16 nmol/L与死亡风险增加相关。目前的结果与先前报道的欧洲受试者数据表明,在不同遗传背景的人群中,新蝶呤与MetS和死亡风险的相关性模式相似。PLP是ifng诱导的色氨酸-犬尿氨酸代谢关键酶的辅助因子。由于PLP缺乏与致糖尿病犬尿氨酸衍生物黄嘌呤酸的产生增加有关,我们的研究结果表明,IFNG产生的上调可能有助于胰岛素抵抗的发展。评估新蝶呤浓度可能有助于监测与衰老相关的医学和精神疾病相关的ifng诱导炎症的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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