儿童营养健康评估_上海迈浦生物科技有限公司

儿童营养健康评估
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相关文献

简介

营养是儿童生长发育的重要基础。幼儿时期是人一生中生长发育最为迅速的。无论是身高、体重、大脑和神经系统都迅速发育。新陈代谢旺盛，活动量随着年龄增长也不断增加。因此，孩子的营养科学性、合理性地安排是极其重要的。不但让孩子吃好，更重要的是吃得科学，吃得合理，吃得健康。所以每天的平衡合理营养尤为重要。也许现在家长们多数认为自己最重视孩子的营养问题。事实上，在这个问题上还存在一些误区。许多家长往往跟着电视广告盲目地追求高营养，却不注重营养的合理性。因此造成幼儿营养缺乏或过剩，影响幼儿的健康成长。那么如何使幼儿的营养合理呢？

儿童营养健康评估是通过采集口腔上皮黏膜细胞，采用SNP分型技术，对儿童DNA中与健康相关的基因位点进行检测分析，主要用于疾病风险的预测和先天体质/特质潜能分析。对儿童健康管理、营养吸收、安全用药有着重要的指导意义。

检测项目

检测项目	基因	临床表现
维生素A代谢能力	BCMO1	抗干眼病因子
维生素B12代谢能力	CLYBL	防止恶性贫血
维生素B6	NBPF3	动脉硬化、秃头、胆固醇过高等
钙吸收能力	GC	出现烦躁、好哭、睡眠不安、易醒、易惊跳、多汗等
硒吸收能力	GPX4	大骨节病、引起中毒
乳糖代谢能力	MCM6	腹泻、严重者可发生脱水、酸中毒、生长迟缓
锌吸收	SLC30A8	味觉嗅觉差、厌食、生长缓慢与智力发育低
维生素C	SLC23A2	坏血病
Ω-3脂肪酸	ALOX5	心脏病、心脑血管疾病、某些癌症、肥胖症、糖尿病、沮丧情绪、心智健康
多动障碍	CLOCK	注意缺陷、活动过多、行为冲动、学习困难、神经系统发育异常、品行障碍、成人ADHD
肥胖症	FTO	食欲极好，喜食油腻、甜食，懒于活动、皮下脂肪丰厚
近视	SLC23A2	视力下降、近视发展速度快、眼球突出、暗适应功能差、眼前黑影
身高	HMGA2	身体成长
音乐潜力	PCDH7	在音乐方面的感知力
记忆能力	WWC1	在短期记忆方面的天赋
肌肉爆发力	ACTN3	肌肉爆发力情况
语言表达能力	Foxp2	语言表达能力
耳垢干湿	ABCC11	耳垢的干湿

参考文献

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions
Genetically determined differences in learning from errors
Bupropion efficacy for smoking cessation is influenced by the DRD2 Taq1A polymorphism Analysis of pooled data from two clinical trials
Dopamine D2 Receptor Polymorphisms and Adenoma Recurrence in the Polyp Prevention Trial
Single Nucleotide Polymorphisms in ANKK1 and the Dopamine D2 Receptor Gene Affect Cognitive Outcome Shortly After Traumatic Brain Injury A Replication and Extension Study
DRD and GRIN2B polymorphisms and their association with the development of impulse control behaviour among Malaysian Parkinson’s disease patients
DRD2ANKK1 Taq1A polymorphism (rs1800497) has opposing effects on D23 receptor binding in healthy controls and patients with major depressive disorder
DRD2ANKK1 TaqIA and SLC6A3 VNTR polymorphisms in alcohol dependence association and gene-gene interaction study in a population of Central Italy
DRD2ANKK1 Taq1A (rs 1800497 CT) genotypes are associated with susceptibility to second generation antipsychotic-induced akathisia
Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1TaqIA on insulin sensitivity
Genetic underpinnings of tardive dyskinesia passing the baton to pharmacogenetics
Sex-specific_influence_of_DRD2_on_ADHD-type_temper
Association between FOXP2 gene and speech sound disorder in Chinese population
Common Kibra alleles are associated with human memory performance
ACTN3 Genotype Is Associated with Human Elite Athletic Performance
Actimetric evidence that CLOCK 3111 TC SNP influences sleep and activity patterns in patients affected by bipolar depression
The association of CLOCK gene T3111C polymorphism and hPER3 gene 54-nucleotide repeat polymorphism with Chinese Han people schizophrenics.
A polymorphism at the 3′-untranslated region of the CLOCK gene is associated with adult attention-deficit hyperactivity disorder
CLOCK gene is implicated in weight reduction in obese patients participating in a dietary programme based on the Mediterranean diet
Two common single nucleotide polymorphisms in the gene encoding β-carotene 15,15′-monoxygenase alter β-carotene metabolism in female volunteers
Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men
Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations.
Common genetic determinants of vitamin D insufficiency a genome-wide association study
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels
Genetic analysis of the vitamin D receptor gene in two epithelial cancers melanoma and breast cancer case-control studies
Vitamin D receptor rs2228570 polymorphism and invasive ovarian carcinoma risk pooled analysis in five studies within the Ovarian Cancer Association Consortium
The short vitamin D receptor is associated with increased risk for generalized aggressive periodontitis
Vitamin D Receptor Polymorphisms and Renal Cancer Risk in Central and Eastern Europe
Association of vitamin D receptor gene variants, adiposity and colon cancer
Circulating 25-Hydroxyvitamin D, VDR Polymorphisms, and Survival in Advanced Non–Small-Cell Lung Cancer
Association Between Single Gene Polymorphisms and Bone Biomarkers and Response to Calcium and Vitamin D Supplementation in Young Adults Undergoing Military Training
Serum selenium and single-nucleotide polymorphisms in genes for selenoproteins relationship to markers of oxidative stress in men from Auckland, New Zealand
Identification of a variant associated with adult-type hypolactasia
Zinc Transporter-8 Gene (SLC30A8) Is Associated with Type 2 Diabetes in Chinese
Effect of zinc supplementation on insulin secretion interaction between zinc and SLC30A8 genotype in Old Order Amish
Polymorphisms in sodium-dependent vitamin C transporter genes and plasma, aqueous humor and lens nucleus ascorbate concentrations in an ascorbate depleted setting
Vitamin C transporter gene (SLC23A1 and SLC23A2) polymorphisms, plasma vitamin C levels, and gastric cancer risk in the EPIC cohort
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease
Effects of 34 risk loci for type 2 diabetes or hyperglycemia on lipoprotein subclasses and their composition in 6,580 nondiabetic Finnish men
NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids
Hangover susceptibility in relation to aldehyde dehydrogenase-2 genotype, alcohol flushing, and mean corpuscular volume in Japanese workers
ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity
Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits
Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1TaqIA on insulin sensitivity
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals Does Heterogeneity of Estimates Relate to Study Design
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium
A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population
Genetic association of refractive error and axial length with 15q14 but not 15q25 in the Blue Mountains Eye Study cohort.
Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height
Common variants in the GDF5-BFZB region are associated with variation in human height
A SNP in the ABCC11 gene is the determinant of human earwax type
Common germline genetic variation in antioxidant defense genes and survival after diagnosis of breast cancer
Genetic variants in selenoprotein genes increase risk of colorectal cancer
Antioxidant-related gene polymorphisms associated with the cardio-ankle vascular index in young Russians
Genetic variation in sodium-dependent ascorbic acid transporters and risk of gastric cancer in Poland
GCK, GCKR, FADS1, DGKBTMEM195 and CDKAL1 Gene Polymorphisms in Women with Gestational Diabetes
Endothelial nitric oxide synthase gene variants and primary open-angle glaucoma interactions with sex and postmenopausal hormone use
Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk
Functional Variants in ADH1B and ALDH2 Coupled With Alcohol and Smoking Synergistically Enhance Esophageal Cancer Risk
A novel polymorphism rs1329149 of CYP2E1 and a known polymorphism rs671 of ALDH2 of alcohol metabolizing enzymes are associated with colorectal cancer in a southwestern Chinese population
Impact of smoking on lung cancer risk is stronger in those with the homozygous aldehyde dehydrogenase 2 null allele in a Japanese population
Candidate gene polymorphisms for diabetes mellitus, cardiovascular disease and cancer are associated with longevity in Koreans
Association of a functional single-nucleotide polymorphism in the ALDH2 gene with essential hypertension depends on drinking behavior in a Chinese Han population
The ALDH2 Glu504Lys polymorphism is associated with coronary artery disease in Han Chinese Relation with endothelial ADMA levels
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The single nucleotide polymorphism upstream of insulin-induced gene 2 ( INSIG2) is associated with the prevalence of hypercholesterolaemia, but not with obesity, in Japanese American women
Dependence of deodorant usage on ABCC11 genotype scope for personalized genetics in personal hygiene