Safety evaluation of genetically modified foods

Authors
Citation
Ma. Martens, Safety evaluation of genetically modified foods, INT A OCCUP, 73, 2000, pp. S14-S18
Citations number
12
Categorie Soggetti
Envirnomentale Medicine & Public Health","Pharmacology & Toxicology
Journal title
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH
ISSN journal
03400131 → ACNP
Volume
73
Year of publication
2000
Supplement
1
Pages
S14 - S18
Database
ISI
SICI code
0340-0131(200006)73:<S14:SEOGMF>2.0.ZU;2-S
Abstract
The concept of substantial equivalence has been accepted as the cornerstone of the health hazard assessment of genetically modified (GM foods (OECD 19 93). Substantial equivalence is the most practical approach to address the safely of foods or food components derived from GM crops and is based on co mparison of the phenotypic and compositional characteristics of the parent crop and the GM crop. Basically, three categories of GM crops can be consid ered (FAO/WHO 1996; EU 1997). (a) GM crops which have the same composition as the parent crop, (b) CM crops which have the same composition as the par ent crop with the exception of a well-defined trait, and (c) GM crops which are different from the parent crop. For the safety assessment of the first category of GM foods only a molecular characterisation of the genetic inse rt is sufficient, whereas for the second category a safety assessment of th e expressed protein(s) is also required. For the last category an extensive evaluation including bioavailability and wholesomeness studies are require d, beside the molecular characterisation and safety assessment of the expre ssed protein(s) and their products. By molecular characterisation is meant the position, nature, stability and number of copies of the inserted DNA. S ubstantial equivalence is established by the determination of the phenotypi c characteristics (e.g. resistance against diseases, agronomic properties) and the complete chemical composition of the plant including nutrients, tox icants. antinutrients, and allergens. The toxicity of the expressed protein (s) is assessed by their homology with known protein toxins, degradation in the gastro-intestinal tract, stability to food processing and acute toxici ty in rodents. The possible allergenicity of the expressed proteins is eval uated by comparison of their amino acid sequence with that of known allerge ns and determination of their stability to digestion and food processing. i f the source of the genetic insert is allergenic then the use of solid-stat e immunoassays, skin prick tests and even food challenge tests can be consi dered.