Thompson Debbie S, Bourdon Celine, Massara Paraskevi, Boyne Michael S, Forrester Terrence E, Gonzales Gerard Bryan, Bandsma Robert H J
Translational Medicine Program, Hospital for Sick Children, Toronto, Canada.
Centre for Global Child Health, Hospital for Sick Children, Toronto, Canada.
JCI Insight. 2020 Dec 17;5(24):141316. doi: 10.1172/jci.insight.141316.
BACKGROUNDSevere acute malnutrition (SAM) is a major contributor to global mortality in children under 5 years. Mortality has decreased; however, the long-term cardiometabolic consequences of SAM and its subtypes, severe wasting (SW) and edematous malnutrition (EM), are not well understood. We evaluated the metabolic profiles of adult SAM survivors using targeted metabolomic analyses.METHODSThis cohort study of 122 adult SAM survivors (SW = 69, EM = 53) and 90 age-, sex-, and BMI-matched community participants (CPs) quantified serum metabolites using direct flow injection mass spectrometry combined with reverse-phase liquid chromatography. Univariate and sparse partial least square discriminant analyses (sPLS-DAs) assessed differences in metabolic profiles and identified the most discriminative metabolites.RESULTSSeventy-seven metabolite variables were significant in distinguishing between SAM survivors (28.4 ± 8.8 years, 24.0 ± 6.1 kg/m2) and CPs (28.4 ± 8.9 years, 23.3 ± 4.4 kg/m2) (mean ± SDs) in univariate and sPLS-DA models. Compared with CPs, SAM survivors had less liver fat; higher branched-chain amino acids (BCAAs), urea cycle metabolites, and kynurenine/tryptophan (KT) ratio (P < 0.001); and lower β-hydroxybutyric acid and acylcarnitine/free carnitine ratio (P < 0.001), which were both associated with hepatic steatosis (P < 0.001). SW and EM survivors had similar metabolic profiles as did stunted and nonstunted SAM survivors.CONCLUSIONAdult SAM survivors have distinct metabolic profiles that suggest reduced β-oxidation and greater risk of type 2 diabetes (BCAAs, KT ratio, urea cycle metabolites) compared with CPs. This indicates that early childhood SAM exposure has long-term metabolic consequences that may worsen with age and require targeted clinical management.FUNDINGHealth Research Council of New Zealand, Caribbean Public Health Agency, Centre for Global Child Health at the Hospital for Sick Children. DST is an Academic Fellow and a Restracomp Fellow at the Centre for Global Child Health. GBG is a postdoctoral fellow of the Research Foundation Flanders.
背景
重度急性营养不良(SAM)是导致全球5岁以下儿童死亡的主要原因。死亡率虽已下降;然而,SAM及其亚型重度消瘦(SW)和水肿型营养不良(EM)的长期心脏代谢后果尚未得到充分了解。我们使用靶向代谢组学分析评估了成年SAM幸存者的代谢谱。
方法
这项队列研究纳入了122名成年SAM幸存者(SW = 69,EM = 53)和90名年龄、性别及体重指数相匹配的社区参与者(CPs),采用直接流动注射质谱联用反相液相色谱法定量血清代谢物。单变量分析和稀疏偏最小二乘判别分析(sPLS - DAs)评估代谢谱差异并确定最具判别力的代谢物。
结果
在单变量分析和sPLS - DA模型中,77种代谢物变量在区分SAM幸存者(28.4 ± 8.8岁,24.0 ± 6.1 kg/m²)和CPs(28.4 ± 8.9岁,23.3 ± 4.4 kg/m²)(均值 ± 标准差)方面具有显著意义。与CPs相比,SAM幸存者肝脏脂肪含量较低;支链氨基酸(BCAAs)、尿素循环代谢物以及犬尿氨酸/色氨酸(KT)比值较高(P < 0.001);β - 羟基丁酸和酰基肉碱/游离肉碱比值较低(P < 0.001),这两者均与肝脂肪变性相关(P < 0.001)。SW和EM幸存者的代谢谱与发育迟缓及未发育迟缓的SAM幸存者相似。
结论
成年SAM幸存者具有独特的代谢谱,表明与CPs相比,其β - 氧化减少,2型糖尿病风险更高(BCAAs、KT比值、尿素循环代谢物)。这表明儿童早期暴露于SAM具有长期的代谢后果,可能随年龄增长而恶化,需要针对性的临床管理。
资助
新西兰健康研究委员会、加勒比公共卫生机构、病童医院全球儿童健康中心。DST是全球儿童健康中心的学术研究员和Restracomp研究员。GBG是弗拉芒研究基金会的博士后研究员。