OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

Similar documents
The Director General Maisons-Alfort, 30 July 2018 OPINION. of the French Agency for Food, Environmental and Occupational Health & Safety

The EFSA scientific opinion on lead in food

Proposed Toxicological Reference Values for Lead (Pb)

OPINION of the French Agency for Environmental and Occupational Health Safety

LOW-LEVEL ENVIRONMENTAL LEAD EXPOSURE AND INTELLECTUAL IMPAIRMENT IN CHILDREN THE CURRENT CONCEPTS OF RISK ASSESSMENT

COMMISSION REGULATION (EU) / of XXX

COMMISSION REGULATION (EU) / of XXX

COLLECTIVE EXPERT APPRAISAL: SUMMARY AND CONCLUSIONS

Public Health Association of Australia: Policy-at-a-glance Environmental Lead Exposure Policy

Experiences with Exposure Models for Estimating the Bioavailability of Lead (Pb) in Children in the EU

COMMISSION DELEGATED REGULATION (EU) /... of XXX

OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

STUDIES TO EVALUATE THE SAFETY OF RESIDUES OF VETERINARY DRUGS IN HUMAN FOOD: GENERAL APPROACH TO ESTABLISH AN ACUTE REFERENCE DOSE

Pesticide risk assessment: changes and perspectives for mammalian toxicology in the new EC regulation 1107/2009

COMMISSION REGULATION (EU) / of XXX. establishing mitigation measures and benchmark levels for the reduction of the presence of acrylamide in food

COMMISSION REGULATION (EU) / of XXX. establishing mitigation measures and benchmark levels for the reduction of the presence of acrylamide in food

Use of modelisation tools to assess risks related to cadmium exposure for workers and consumers

Determination of new lead exposure risk management objectives

Statement on the ANSES reports on bisphenol A 1

COMMISSION REGULATION (EU)

Lead Poisoning: CDC s New Target for Prevention

INTERNATIONAL CONCIL FOR HARMONISATION OF TECHNICAL REQUIREMENTS FOR PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED GUIDELINE Q3D(R1)

HEALTH CONSULTATION. Tom Lea Park EL PASO COUNTY METAL SURVEY EL PASO, EL PASO COUNTY, TEXAS EPA FACILITY ID: TX

COMMISSION DELEGATED REGULATION (EU) /... of XXX

EU policy on acrylamide in food reducing human exposure to ensure a high level of human health protection

Delegations will find attached document D048379/05.

OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

Maisons-Alfort, 3 July 2009 OPINION

All member States were represented, except Bulgaria and Czech Republic

COLLECTIVE EXPERT APPRAISAL: SUMMARY AND CONCLUSIONS

Parma, 21/09/2015 SCIENTIFIC EVALUATION OF REGULATED PRODUCTS DEPARTMENT

Emanuela Turla Scientific Officer Nutrition Unit - EFSA

Integrated Exposure Uptake Biokinetic (IEUBK) Model for Lead in Children

Ongoing review of legislation on cadmium in food in the EU: Background and current state of play

COMMISSION DELEGATED REGULATION (EU).../... of XXX

The terms used in these Directives are consistent with those defined by the Committee.

Food Safety Risk Assessment and Risk Management at a European Level

WORKING DOCUMENT DOES NOT NECESSARILY REPRESENT THE VIEWS OF THE EUROPEAN COMMISSION SERVICES

of the French Agency for Food, Environmental and Occupational Health & Safety

OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

DRAFT COMMISSION DELEGATED REGULATION (EU) /... of XXX

Minutes of EFSA-ANSES Expert Meeting on Bisphenol A (BPA) Art. 30 Regulation (EC) No 178/2002 Held on 3 December 2014, Paris (France)

FAQs on bisphenol A in consumer products

Welcome and introduction to EFSA

European public MRL assessment report (EPMAR)

Findings and Recommendations of the Fluoride Expert Panel (January 2007)

Using science to establish effective food safety control for the European Union Dr David Jukes

Opinion on Voluntary Risk Assessment Report on lead and lead compounds. Human Health Part

Regarding Establishment of a Uniform Limit in a Positive List System concerning Agricultural Chemicals Residues in Food etc.

COMMISSION REGULATION (EU) / of XXX

The legal basis of this draft Regulation is Art. 11 (4) of Regulation (EC) No. 882/2204.

COMMISSION REGULATION (EU) No /.. of XXX. amending Regulation (EC) No 1881/2006 as regards maximum levels of lead in certain foodstuffs

EFSA PRE-SUBMISSION GUIDANCE FOR APPLICANTS INTENDING TO SUBMIT APPLICATIONS FOR AUTHORISATION OF HEALTH CLAIMS MADE ON FOODS

Trilateral meeting on perchlorate risk assessment Trilateral meeting report of the meeting on , Parma. (Agreed on )

Official Journal of the European Union. (Non-legislative acts) REGULATIONS

PART I : List of documents

OPINION of the French Agency for Food, Environmental and Occupational Health & Safety

French cooperation with EFSA

*-efsa. Parma, 1 3 APR 2012 Ref. CGL/PB/AF/AFC/emf(2012) - out

Health Risks Analysis of Lead due to the Consumption of Shellfish (Anadara. Sp) among the Coastal Communities in Makassar City

MEDICAL SCIENCES - Vol.II -The Need For an International Approach The Role of FAO and WHO - Jorgen Schlundt and Kazuaki Miyagishima

L 32/44 Official Journal of the European Union

Perfluoroalkylated substances in food - EFSA Assessments

Gestion du plomb dans l eau potable l approche québécoise de santé publique

COMMISSION STAFF WORKING DOCUMENT 1. Review report for the active substance Copper compounds

Questions and Answers on Candidates for Substitution

Scientific Panel on Plant Protection Products and their Residues

Lead Paint Alliance Toolkit for Establishing Laws to Control the Use of Lead in Paint. Patrick Huber US Environmental Protection Agency

EFSA Statement regarding the EU assessment of glyphosate and the socalled

REASONED OPINION. European Food Safety Authority 2, 3. European Food Safety Authority (EFSA), Parma, Italy

Practical guidance for applicants on the submission of applications on food additives, food enzymes and food flavourings

1 OJ L 354, , p OJ L 80, , p. 19.

Evaluation of proposed new HBV for lead in drinking water Ian Douglas July, 2016

Poly-fluoroalkyl substances (PFASs), also called perfluoroalkyl substances (PFASs)

Genotoxicity Testing Strategies: application of the EFSA SC opinion to different legal frameworks in the food and feed area

TDS Exposure Assessment Tool MCRA

The role of the national & European reference laboratories

EUROPEAN COMMISSION SUMMARY REPORT OF THE STANDING COMMITTEE ON PLANTS, ANIMALS, FOOD AND FEED HELD IN BRUSSELS ON 09 JUNE 2015

Aflatoxins (sum of B1, B2, G1, G2) in cereals and cereal-derived food products 1

Maisons-Alfort, 10 January 2007 OPINION

Prevention of exposure to lead, international aspects

REGULATION concerning Marketing Authorisations for Natural Medicinal Products and Registration of Traditional Herbal Medicinal Products, No. 142/2011.

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

From risk assessment to risk management focus on contaminants. Frans Verstraete European Commission DG Health and Consumer Protection

DIRECTIVE 2004/24/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL. of 31 March 2004

EMEA WORKING PARTY ON HERBAL MEDICINAL PRODUCTS

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

Comments from PlasticsEurope

EUROPEAN COMMISSION SUMMARY REPORT OF THE STANDING COMMITTEE ON PLANTS, ANIMALS, FOOD AND FEED HELD IN BRUSSELS ON 23 SEPTEMBER 2015

Provisional Translation Original: Japanese

SANCO/10616/2009 rev. 7 ( )

Guidance on the review, revision and development of EFSA s cross-cutting guidance documents

PREPERATION OF TURKEY TO EFSA ACTIVITIES

Recent Developments and Future Plans in the EFSA Assessments of Pesticides. Hermine Reich Pesticides Unit

Evaluation of active substances in plant protection products Residues Anja Friel European Food Safetey Authority, Parma/ Italy

COMMISSION REGULATION (EU) No /.. of XXX

Lead Toxicity. How does it get from those forms inside humans?

EFSA Info Session Pesticides 26/27 September Anja Friel EFSA Pesticides Unit (Residues team)

Application of human epidemiological studies to pesticide risk assessment

Transcription:

The Director General Maisons-Alfort, 23 January 2013 OPINION of the French Agency for Food, Environmental and Occupational Health & Safety on the health effects of blood lead levels below 100 µg/l ANSES undertakes independent and pluralistic scientific expert assessments. ANSES primarily ensures environmental, occupational and food safety as well as assessing the potential health risks they may entail. It also contributes to the protection of the health and welfare of animals, the protection of plant health and the evaluation of the nutritional characteristics of food. It provides the competent authorities with all necessary information concerning these risks as well as the requisite expertise and scientific and technical support for drafting legislative and statutory provisions and implementing risk management strategies (Article L.1313-1 of the French Public Health Code). Its opinions are made public. This opinion is a translation of the original French version. In the event of any discrepancy or ambiguity the French language text dated 23 January 2013 shall prevail. On 26 July 2011, ANSES received a request by the Directorate General of Health and the Directorate General for Risk Prevention (Ministry of the Environment) to investigate exposure to lead. 1. BACKGROUND AND PURPOSE OF THE REQUEST The report entitled Lead in Food, published in April 2010 by the European Food Safety Authority (EFSA), mentions developmental neurotoxic effects in children as well as cardiovascular and kidney effects, associated with blood lead levels below 100 µg/l. These data raise questions about the scientific basis for the threshold currently applied to treat children (blood lead levels above 100 µg/l) and about the public health measures that need to be taken to limit exposure of the general population to lead. The Request concerned the following three questions: 1 Do the studies suggesting that blood lead levels below 100 µg/l can have harmful effects provide a sufficiently robust scientific basis to justify taking specific riskmanagement measures? 2 Have these questions been raised in other EU countries? If so, what measures and technical actions have been taken to bring blood lead levels below 100 µg/l? French Agency for Food, Environmental and Occupational Health & Safety, 27-31 av. du Général Leclerc, 94701 Maisons-Alfort Cedex - Telephone: + 33 (0)1 49 77 13 50 - Fax: + 33 (0)1 49 77 26 26 - www.anses.fr 1 / 6

3 Is it possible to establish one or more critical doses on which to base the management of moderate blood lead levels 1, and if so, for which population group and concerning which effects? The study will exclude the population of workers exposed to lead. 2. ORGANISATION OF THE EXPERT APPRAISAL The expert appraisal was carried out in accordance with French standard NF X 50-110 Quality in Expert Appraisals General Requirements of Competence for Expert Appraisals (May 2003). The Agency entrusted examination of Request for an Opinion on exposure to lead to the Expert Committee (CES) on Assessment of the risks related to chemical substances. The CES mandated the Working Group on Toxicity reference values 1 (VTR 1) to carry out the assessment. An initial collective expert report on the first phase of the work (Questions 1 and 2) was validated by the CES on 19 January 2012. Membership of the VTR Working Group was then renewed and the new WG (VTR 2) was formed on 25 October 2011. The VTR 2 Working Group was then mandated to address the third question. The experts examined the plausibility of the effects of moderate blood lead levels taking especially into account the effects on the central nervous system, the kidneys, the cardiovascular system, the reproductive system and the immune system. For this purpose, it mainly leant on EFSA s Lead in Food report (2010), on the Human Health State of the Science Report on Lead report by Health Canada (2011), and also the report of the US National Toxicology Program (NTP, 2012). The work of the VTR 2 Working Group was submitted at regular intervals to the CES. This report completes and replaces the interim report on the health effects associated with blood lead levels below 100 µg/l. The work for the report gave rise to a collective expert appraisal memorandum that was adopted by the CES on Assessment of the risks related to chemical substances on 25 October 2012. It should be noted that two experts in the VTR WG expressed divergent opinions on the expert report. Their positions are laid out in the Divergent Positions section of the report. 3. ANALYSIS AND CONCLUSIONS OF THE CES The answers to the questions asked by the Directorate General for Health and the Directorate general for Risk Prevention expressed in the official Request are given below: 1 Do the studies suggesting that blood lead levels below 100 µg/l can have harmful effects provide a sufficiently robust scientific basis to justify taking specific risk-management measures? An analysis of the epidemiological data describing associations between blood lead levels and various health effects was carried out, on the basis of the source studies, meta- 1 Moderate lead levels: blood levels of lead below the regulatory threshold of 100 μg/l. 2 / 6

analyses, analysis of pooled published data and recent expert assessments from international (EFSA) and national organisations (Health Canada and the NTP). The expert collective concluded that the studies showing the effects of lead on blood pressure and kidney functions in adults and those showing an adverse effect on the central nervous system (measured by a decrease in IQ) in children, provide a sufficiently robust scientific basis for concluding that lead can have adverse effects at blood levels below 100 µg/l. These conclusions concur with those expressed by the other international and national organisations mentioned above that have recently assessed the effects of lead. 2 Have these questions been raised in other EU countries? If so, what measures and technical actions have been taken to bring blood lead levels below 100 µg/l? In January 2012, ANSES consulted the Member States of the European Union (EU), the Accession Candidate Countries and the countries belonging to the European Free Trade Association (EFTA) on the measures and technical actions taken to bring blood lead levels below 100 µg/l. Ten countries responded, none of which reported having taken any specific measures. 3 Is it possible to establish one or more critical doses on which to base the management of moderate blood lead levels, and if so, for which population group and concerning which effects? The expert collective considered that the most sensitive and conclusive effects related to chronic exposure to lead are chronic kidney disease 2 in adults, and neurotoxicity in young children. Based on the study by Lanphear et al. (2005), EFSA established a critical blood lead level for children of 12 µg/l, this level being associated with a drop of one point of Intellectual Quotient (IQ) in a population. On the basis of the available information and the additional hearings held by the Working Group on the significance that may be attributed to a reduction of one point of IQ, the experts considered that: - IQ tests were not developed for the purpose of assessing the neurotoxicity of chemicals, - the determination of IQ is subject to wide intra- and inter-individual variations as well as variations in test conditions, - a drop of one point of IQ may be statistically significant across an entire population but is not significant at individual level, - due to the lack of data and to analytical limitations, it is difficult to correlate IQ with blood lead levels below 10 µg/l. The expert group considered that a reduction of one point of IQ cannot be used for a quantitative assessment of the health risk. The expert group also considered that a blood lead level established with kidney effects in adults as the critical effect would protect the entire population, including children, against all the adverse effects of lead identified to date. The study by Navas-Acien et al. (2009) of the NHANES 1999 2006 survey was chosen as the key study for defining kidney toxicity of lead and for establishing critical blood lead levels (BMD 10% and BMD 10% L 95% ). This study, on 14,778 subjects over the age of 20, 2 Chronic kidney disease is defined as a glomerular filtration rate of less than 60 ml/1.73 m 2 of body surface area/min for more than 3 months. Evaluation de la fonction rénale et de la protéinurie pour le diagnostic de la maladie rénale chronique chez l adulte [Evaluation of glomerular filtration rate and proteinuria for the diagnosis of chronic kidney disease]. Nephrol Ther 2009; 5:302-305. 3 / 6

showed associations between blood levels of lead and reduction in glomerular filtration rate. On the basis of this study, EFSA modelled the relationship between lead levels and the prevalence of chronic kidney disease (defined by the persistence for longer than 3 months of a glomerular filtration rate of less than 60 ml/min/1.73 m 2 of body surface area). A critical blood lead level of 15 µg/l was determined (the value associated with an increase of 10% in the prevalence of chronic kidney disease). This value can be considered as protecting against effects on the central nervous system in children. No kidney effect was observed in children (under the age of 12) for blood lead levels below 50 µg/l (NTP, 2012). Kidney effects observed in adults may be consecutive to lifetime exposure (since childhood). Consequently, nephrotoxicity was selected as the critical effect for the entire population irrespective of age. Levels of atmospheric and oral exposure to lead can be estimated in children up to the age of 7, using the Integrated Exposure Uptake Biokinetic 3 (IEUBK) model developed by the US EPA (US EPA, 1994), and in adults using the equation of Carlisle and Wade 4. In children, for example, daily exposure by the oral route (assuming negligible exposure by contact with soil) of 0.63 µg of lead per kilo of body weight per day would result in a blood lead level of 15 µg/l. 3 http://www.epa.gov/superfund/lead/products.htm#ieubk. Integrated Exposure Uptake Biokinetic Model for Lead in Children, Windows version (IEUBKwin v1.1 build 11) (February, 2010) 32-bit version 4 Lead level (μg/l) = [dietary exposure (μg/kg/day) x weight x 0.4] + [concentration in soil and dust (mg/kg) x 0.025 x 0.18] + [atmospheric concentration (µg/m 3 ) x 16.4]. 4 / 6

4. AGENCY CONCLUSIONS AND RECOMMENDATIONS The French Agency for Food, Environmental and Occupational Health & Safety endorses the conclusions and recommendations of the CES on Assessment of the risks related to chemical substances, on the health effects of lead associated with blood lead levels below 100 µg/l. The Agency emphasises that: - in France, 50% of children in the 1 to 6 age range and 75% of adults in the 18 to 74 age range present blood lead levels in excess of 15 μg/l (see the survey Imprégnation des enfants par le plomb en France en 2008-2009, Etchevers et al. 2010, and the National Nutrition & Health Study discussed in Fréry et al., 2011); - dietary exposure (foodstuffs and drinking water) is the principal route of exposure to lead. According to the Total Diet Study 2 (TDS 2) (ANSES 2011), mean dietary exposure to lead of the French population is estimated at 0.20 μg/kg bw/day in adults and 0.27 μg/kg bw/day in children. At the 95 th percentile, exposure is estimated at 0.35 µg/kg bw/day in adults and at 0.57 µg/kg bw/day in children. Domestic dust and soil contaminated by lead are also an important source of exposure in children. The Agency also recommends: - in view of the new data available, reviewing all the reference values based on blood lead levels, including those applicable in occupational environments, - continuing with efforts to reduce the exposure of the population to lead, - continuing biomonitoring studies in order to monitor blood lead levels for the entire population. The Director General Marc Mortureux 5 / 6

KEY WORDS Lead, IQ, neurotoxicity, nephrotoxicity, cardiotoxicity, toxicity reference values, critical dose, uncertainty factors, health effects, general population, children References ANSES-French Total Diet Study 2 (TDS 2) Edition scientifique, June 2011, Volume 1 p.41. Etchevers A, Lecoffre C, Le Tertre A, Le Strat Y, Groupe Investigateurs Saturn-Inf, De Launay C, et al. Imprégnation des enfants par le plomb en France en 2008-2009 [Blood lead level in children in France, 2008-2009]. BEH 2010. European Food Safety Authority (EFSA), Parma, Italy, Scientific Opinion on Lead in Food, EFSA panel on contaminants in the Food Chain (CONTAM) EFSA Journal 2010; 8(4):1570. Fréry N, Saoudi A, Garnier R, Zeghnoun A, Falq G. Exposition de la population française aux substances chimiques de l'environnement. Saint-Maurice: Institut de veille sanitaire; 2011. 151 p. Health Canada. Draft Human Health State of the Science Report on Lead, 2011. Lanphear BP, Hornung R, Khoury J, Yolton K, Baghurst P, Bellinger DC, Canfield RL, Dietrich KN, Bornschein R, Greene T, Rothenberg SJ, Needleman HL, Schnaas L, Wasserman G, Graziano J, Roberts R. Low-level environmental lead exposure and children's intellectual function: an international pooled analysis. Environ Health Perspect. 2005 Jul; 113(7):894-9. National Toxicology Program; NTP Monograph on Health Effects of Low-Level Lead - October 14, 2012. Navas-Acien A, Tellez-Plaza M, Guallar E, Muntner P, Silbergeld E, Jaar B, Weaver V. Blood cadmium and lead and chronic kidney disease in US adults: a joint analysis. Am J Epidemiol. 2009 Nov 1;170(9):1156-64. 6 / 6