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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.

Cover of Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline

Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid, Biotin, and Choline.

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PGlossary and Abbreviations

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

Copyright © 1998, National Academy of Sciences.
Bookshelf ID: NBK114323

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