NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.
Institute of Medicine (US) Standing Committee on the Scientific Evaluation of Dietary Reference Intakes and its Panel on Folate, Other B Vitamins, and Choline. Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline. Washington (DC): National Academies Press (US); 1998.
Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline.
Show details- ACC
Acetyl-CoA carboxylase
- ADP
Adenosine diphosphate
- AI
Adequate Intake
- ALT
Alanine aminotransferase
- apABG
Acetamidobenzoylglutamate
- ATP
Adenosine triphosphate
- Bioavailability
The accessibility of a nutrient to participate in metabolic and/or physiological processes.
- BMI
Body mass index; weight/height2 (kg/m2)
- CHD
Coronary heart disease
- CI
Confidence interval
- CoA
Coenzyme A
- CSFII
Continuing Survey of Food Intakes by Individuals, a survey conducted by the Agricultural Research Service, USDA
- CV
Coefficient of variation
- DFE
Dietary folate equivalent
- DNA
Deoxyribonucleic acid
- Dose-response assessment
The step in a risk assessment in which the relationship between nutrient intake and adverse effect (in terms of incidence and/or severity of the effect) is determined.
- DRI
Dietary Reference Intake
- α-EALT
Erythrocyte alanine aminotransferase
- EAR
Estimated Average Requirement
- α-EAST
Erythrocyte aspartate aminotransferase
- EEG
Electroencephalogram
- EGR
Erythrocyte glutathione reductase
- EGRAC
Erythrocyte glutathione reductase activity coefficient
- ETK
Erythrocyte transketolase
- ETKAC
Erythrocyte transketolase activity coefficient
- FAD
Flavin-adenine dinucleotide
- FAO
Food and Agriculture Organization of the United Nations
- FIGLU
Formiminoglutamic acid
- FMN
Flavin mononucleotide
- FNB
Food and Nutrition Board
- Hazard identification
The step in a risk assessment, which is concerned with the collection, organization, and evaluation of all information pertaining to the toxic properties of a nutrient.
- HIV
Human immunodeficiency virus
- HPLC
High-performance liquid chromatography
- HPV
Human papilloma virus
- IM
Intramuscular
- IOM
Institute of Medicine
- LCAT
Lecithin-cholesterol acyltransferase
- LOAEL
Lowest-observed-adverse-effect level; the lowest intake (or experimental dose) of a nutrient at which an adverse effect has been identified.
- MCV
Mean cell volume
- MI
Myocardial infarction
- MMA
Methylmalonic acid
- MTHFR
Methylenetetrahydrofolate reductase
- NAD
Nicotinamide adenine dinucleotide
- NADP
Nicotinamide adenine dinucleotide phosphate
- NAS
National Academy of Sciences
- NE
Niacin equivalent
- NHANES
National Health and Nutrition Examination Survey, a survey conducted periodically by the National Center for Health Statistics, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services
- NHIS
National Health Interview Survey, a survey conducted periodically by the National Center for Health Statistics, Centers for Disease Control and Prevention, U.S. Department of Health and Human Services
- NOAEL
No-observed-adverse-effect level; the highest intake (or experimental dose) of a nutrient at which no adverse effect has been observed.
- NRC
National Research Council, the organizational arm of the National Academies
- NTD
Neural tube defect
- 4-PA
4-Pyridoxic acid
- pABG
p-Aminobenzoylglutamate
- PARP
Poly-ADP-ribose polymerase
- PGA
Pteroylglutamic acid
- PL
Pyridoxal
- PLP
Pyridoxal phosphate
- PM
Pyridoxamine
- PMP
Pyridoxamine phosphate
- PN
Pyridoxine
- PNP
Pyridoxine phosphate
- RDA
Recommended Dietary Allowance
- Risk
Within the context of nutrient toxicity, the probability or likelihood that some adverse effect will result from a specified excess intake of a nutrient.
- Risk assessment
An organized framework for evaluating scientific information that has as its objective a characterization of the nature and likelihood of harm resulting from excess human exposure to an environmental agent (in this case, a dietary nutrient). It includes the development of both qualitative and quantitative expressions of risk. The process of risk assessment can be divided into four major steps: hazard identification, dose-response assessment, exposure assessment, and risk characterization.
- Risk characterization
The final step in a risk assessment, which summarizes the conclusions from the other three steps of the risk assessment and evaluates the risk. This step also includes a characterization of the degree of scientific confidence that can be placed in the UL.
- Risk management
The process by which risk assessment results are integrated with other information to make decisions about the need for, method of, and extent of risk reduction. In addition to risk assessment results, risk management considers such issues as the public health significance of the risk, technical feasibility of achieving various degrees of risk control, and economic and social costs of this control.
- SD
Standard deviation
- SE
Standard error
- SEM
Standard error of the mean
- TCI, II, III
Transcobalamin I, II, and III
- TMA
Trimethylamine
- TPN
Total parenteral nutrition
- TPP
Thiamin pyrophosphate
- UL
Tolerable Upper Intake Level
- UF
Uncertainty factor; a number by which the NOAEL (or LOAEL) is divided to obtain the UL. UFs are used in risk assessments to deal with gaps in data (e.g., data uncertainties) and knowledge (e.g., model uncertainties). The size of the UF varies depending on the confidence in the data and the nature of the adverse effect.
- USDA
U.S. Department of Agriculture
- WHO
World Health Organization
- Glossary and Abbreviations - Dietary Reference Intakes for Thiamin, Riboflavin, ...Glossary and Abbreviations - Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline
Your browsing activity is empty.
Activity recording is turned off.
See more...