新生儿的性饮食:影响,陷,以及由酸盐脱酶缺乏症影响的早产新生儿的范例
Sokratis Katsoudas1, Luis A Umana2, Rebekah Clarke3
1Department of Pediatrics, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
概括
性饮食 (KD) 很少在新生儿中使用,主要用于代谢和性疾病. 这次审查考察了KD.
科学领域:
- 新生儿医学 新生儿医学
- 营养科学 营养科学
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 在新生儿中性饮食 (KD) 的应用是不常见的,通常是针对特定的代谢和症状.
- 关于早产婴儿的KD影响的数据有限,大多数信息来自病例报告.
研究的目的:
- 审查最近的进展,指示,机制和切性饮食在新生儿中使用的实际方面.
- 介绍一个早产婴儿的病例研究,该婴儿患有酸盐脱酶缺乏症,并与KD进行治疗.
主要方法:
- 关于KD在新生儿中的最新进展和应用的文献综述.
- 病例报告详细介绍了在KD.上治疗和结果的早产婴儿与pyruvate脱酶缺乏.
主要成果:
- 该综述综合了新生儿护理中关于KD的当前知识.
- 案例报告说明了管理KD新生儿代谢障碍的复杂性和挑战.
结论:
- 性饮食在新生儿代谢障碍管理中提出了独特的挑战和考虑.
- 需要进一步的研究,以建立最佳的KD协议,为早产婴儿与特定的代谢条件.
相关概念视频
Inborn Errors of Metabolism
697
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
697
Pharmacokinetics in Pediatric Patients: Drug Metabolism
195
In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
195
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
246
Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
246
Fates of Pyruvate
10.5K
Pyruvate is the end product of glycolysis, where glucose is oxidized to pyruvate, simultaneously reducing NAD+ to NADH. Two molecules of ATP are also produced by substrate-level phosphorylation.
In aerobic organisms, pyruvate is metabolized via the citric acid cycle to produce reduced coenzymes NADH and FADH2. These coenzymes are then oxidized in the electron transport chain to produce ATP and, in the process, regenerate the NAD+ and FAD. As seen in some cell types and organisms, fermentation...
In aerobic organisms, pyruvate is metabolized via the citric acid cycle to produce reduced coenzymes NADH and FADH2. These coenzymes are then oxidized in the electron transport chain to produce ATP and, in the process, regenerate the NAD+ and FAD. As seen in some cell types and organisms, fermentation...
10.5K
Pharmacokinetics in Pediatric Patients: Drug Distribution
254
Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight,...
254
Pyruvate Oxidation
168.3K
After glycolysis, the charged pyruvate molecules enter the mitochondria via active transport and undergo three enzymatic reactions. These reactions ensure that pyruvate can enter the next metabolic pathway so that energy stored in the pyruvate molecules can be harnessed by the cells.
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...
168.3K


