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Perchlorate The State of the Science Human Studies Offie Porat Soldin, Ph.D. Consultants in Epidemiology and Occupational Health, Inc. Washington, D.C. 12-12- 2001 Outline • Thyroid • Occupational • NIS • Environmental – Neonatal – Pediatric – Adult – Cancer – Clinical studies • Perchlorate • Exposure ranges Perchlorate (ClO4-) ion Characteristics • A halogen Oxyanion: ClO4-1 Perchlorate One “extra” oxygen atom Tetrahydron ClO3 –1 Chlorate Most common form ClO2-1 Chlorite One less oxygen atom ClO-1 Hypochlorite Two fewer oxygen atoms Perchlorate (ClO4-) ion properties •High chemical stability. The reduction of Cl from a +7 oxidation state to –1 as a chloride requires energy or a catalyst and does not occur spontaneously •Hygroscopic. Highly water soluble (AP is 20g/100g solution @ 25oC) • Exceedingly mobile in aqueous systems • Density nearly twice that of water • Can persist for decades due to kinetic barriers to its reactivity with other constituents The Sodium-Iodide Symporter (NIS) • Controls the uptake of iodine by the thyroid • An intramembrane protein of 65kD • Co-transports iodide (I-) with two sodium (Na+) ions against an electrochemical gradient • Iodine thyroid/plasma gradient equals 25: 1 to 500: 1 The Sodium-Iodide Symporter Iodine Age Group Recommended I2 intake (μg/day) Adults Pregnant women Lactating women Adolescents Children Fetus in uteri, Neonates and 150 175 200 150 90-120 90 Effects of Iodine Deficiency Disorders Adult Goiter with its Complications Thyroid Deficiency Impaired Mental Function Child Goiter Thyroid Deficiency Impaired School Performance Retarded Physical Development Neonate Neonatal Goiter Brain Damage Neurobehavioral Fetus Abortion Stillbirths Brain Damage - Cretinism Pregnancy and Thyroid Function – The Mother • Iodine clearance by the kidney increases increased glomerular filtration • Iodine and iodothyronines transferred to fetus • Women living in low iodine intake areas may develop iodine deficiency and enlarged thyroid • The hypothalamic-pituitary-thyroid axis functions normally in pregnant women with adequate iodine Thyroid Adequacy Maternal Fetal Outcome + + Good + - - + Good if treated early May not be good - - Bad Pregnancy and Thyroid Function – Fetus / Neonate I • Maternal hypothyroidism can be associated with neonatal defects (mental deficiency/ neurological defects/ low or normal IQs) • If infants have low T3 and T4 levels and elevated TSH levels, early appropriate treatment results in a normal intellect Pregnancy and Thyroid Function – Fetus / Neonate II • NIS presence in mammary glands leads to secretion of iodine in milk, which is probably important for thyroid function in neonates • Prolactin stimulates NIS production which is inhibited by most anti-thyroidal agents, but not by perchlorate ClO4- in water - Detection • 1997 – Ion chromatography, assay sensitivity improved from 400ppb to 4 μg/L (4 ppb) • Public water supplies found to contain perchlorate ions: S California - 5-8 ppb; S Nevada - 5-24 ppb • Method modified for ClO4- detection in urine (LOD 500 ppb) and serum (LOD 50 ppb) • Electrospray ionization (ESI/MS/MS) (LOD 0.5 ppb) Less signal suppression by nitrate, bicarbonate and sulfate Perchlorate Potential Exposure Potential Risk • • • • • Pathologic Therapeutic Pharmacology Occupational Environmental • • • • Neonatal Pediatric Adult Cancer Reported Deaths from Bone Marrow Toxicity among Perchlorate-treated Thyrotoxicosis Patients Daily Dosage (mg/day) Body Weight Adjusted Daily Dosage (mg/kg/day) Length of Treatment for each case Hobson 1961 800 600 11 9 14 weeks 20 weeks Fatal aplastic anemia Johnson & Moore 1961 1000 600 14 9 3 months 1 month Fatal aplastic anemia Fawcett & Clark 1961 600 400 9 6 5 months 1-2 months Fatal aplastic anemia Krevans et al. 1962 800 600 450 11 9 6 2 weeks 2 months 2 months Gjemdal 1963 600 400 9 6 3 months 1 month Fatal aplastic anemia Barzilai and Sheinfeld 1966 1000 14 2 months Fatal aplastic anemia 1000 14 Few Months Fatal agranulocytosis Study Effects Fatal aplastic anemia Therapeutic use of ClO4Indication Dosage Hyperthyroidism 600-900 mg/day Hyperthyroidism in pregnancy 600-1000 mg/day Amiodarone induced (treatment for resistant tachyarryhthmias) 800-1000 mg/day then 16 months at lower doses Perchlorate Pharmacology I • Pharmacology – – – – – – rapidly absorbed excreted intact in the urine half-life: 5-8 hr (humans) 95% recovered in urine over 72 hr similar ionic size to iodide competitive inhibitor of NIS Perchlorate Pharmacology II – May not be translocated into the thyroid cell – Ki is estimated as 0.4-24 μM – May inhibit iodide accumulation → goiter1 and lead to hypothyroidism if iodine intake low < 50-150 μg/day – May inhibit organic binding of iodine by affecting thyroid peroxidase (not proven) 1 Toxic multinodular goiter (Plummer’s disease) refers to an enlarged multinodular goiter commonly found in areas of iodine deficiency in which patients with long-standing non-toxic goiter develop thyrotoxicosis Perchlorate Diagnostic Use • The perchlorate discharge test - detect iodide organification defects (1000 mg) • Pertechnetate (Tc 99m) radiological studies to image brain, blood pool, localize the placenta. Pretreatment: 200-400 mg ClO4- minimizes pertechnetate in thyroid, salivary glands and choroid plexus • Perchlorate is used to block the gastric uptake of Tc 99m in the investigation of GI bleeding Perchlorate Epidemiological Studies Occupational Exposure • To determine exposure levels and potential health effects need to estimate a safe working level of perchlorate • Much higher than environmental • Exposure: inhalation, ingestion, or dermal contact • Significant systemic absorption likely because of the high aqueous solubility at body temperature • USA: No occupational standard for perchlorate • OSHA regulates perchlorate as a nuisance dust (limit of 15 mg/m3 (time-weighted average) • Safety concerns – it has explosive potential Occupational Studies • Gibbs et al. (1998) Nevada • Cumulative exposure – Average lifetime dose: 38 mg/kg – No adverse effects on thyroid • Shift exposure – Inhaled dose: 0.2-436 g/kg (ave 36 g/kg) • Lamm et al. (1999) Utah • Cross sectional • Individual exposure – Pre- post-shift urine • Group exposure – 3 exposures & control group – Urine: 0.9 – 34 mg/shift (LOD=500 ppb) – Serum: 110 – 1600 ppb (LOD 50 ppb) • No adverse effects on thyroid function 0.01-34 mg/day Perchlorate Exposure • Environmental • • • • Neonatal Pediatric Adult Cancer • Clinical Studies Neonatal Studies Environmental exposure •Neonatal screening routine in most of the developed world •Congenital hypothyroidism (CH) treatable if caught early enough • 3. Neonatal TSH - Las Vegas • 1. CH data – no CH (+ ClO4-) neonates compared increase in exposed areas with Reno (-) Perchlorate exposure had no • 2. T4 - Las Vegas (+ ClO4effect 15ppb) neonates compared with Reno(-) • 4.Chile – neonatal TSH No ClO4- effect (n=9,784). (100-120 ppb compared to low exposures • Brechner -Arizona 5-7 and <4ppb) No differences found in TSH levels Pediatric Studies Environmental exposure • Children and adolescents at greatest risk for low I2 • Crump et al. studied school-age children (n = 162) • 100-120 ppb, 5-7ppb and < 4ppb ClO4- in their drinking water • No differences found in TSH, FT4 and goiter prevalence Adult Studies Environmental exposure • Nevada Medicaid database (1997-1998) • Prevalence of thyroid diseases in areas exposed to ClO4- vs. areas unexposed • The prevalence rates of thyroid diseases was no greater in areas exposed to ClO4- in drinking water Thyroid Cancer Studies Environmental exposure • Risk measures of thyroid cancer – Prevalence, Mortality, Incidence • All 3 measures showed no association with ClO4- exposure • ClO4- is non-mutagenic Prospective Volunteer Studies I • 900 mg/day ClO4- for 4 wks – FT4 decreased; thyroid gland not depleted of iodine (Brabant et al. 1992) • Iodine uptake inhibition studies (Lawrence et al. 2001) • Thyroid function studies and iodine-uptake studies (prior/ during 2 wk exposure (3 mg or 10 mg ClO4-)/ 2 wks postexposure • No effect on thyroid function studies (T4, T3, FTI, thyroid hormone binding ratio & TSH) •10 mg/day dosage •38 % inhibition of iodine uptake •Serum ClO4- levels: 0.6 μg/ml (6 μM) •3 mg/day dosage •Serum ClO4- levels: below detection limit •A linear-log regression predicted a no-effect level of 2 mg/day Prospective Volunteer Studies II • • • • Greer et al. (2000) 35 mg/day, 7 mg/day, 1.4 mg/day and 0.5 mg/day Found a significant inhibition of iodine uptake A linear-log regression predicted a no-effect level of 0.5 mg/day • 0.5 mg/day had no effect on iodine uptake • The data indicated a no-effect on iodine uptake level equivalent to an environmental ClO4drinking water level of 250 μg/L Perchlorate dose-response in humans exposed therapeutically, occupationally, in clinical studies or environmentally via drinking water Effect / endpoint Fatal hemotoxicity (aplastic anemia) Non-fatal hemotoxicity (blood-dyscrasias, including agranulocytosis) Therapeutic Effect Range for Amiodarone treatment Pharmacological Effect Range (normalization of thyroid function in hyperthyroid patients) Calculated Safe Occupational Average (BMDL) Demonstrated Safe Occupational Average ii No-effect level for TSH elevation in newborns iii (Environmental Level 5-25 ppb) i Daily Dose Body-Weight Adjusted Daily Dose i 1000 - 2000 mg 15-30 mg/kg 600–1000mg 400 mg agranulocytosis 8.5-14 mg/kg 5.7 mg/kg 1000 mg start followed by 100 mg 12.8 mg/kg then 1.4 mg/kg 200-1000 mg 2.8 – 14 mg/kg 50 mg 0.7 mg/kg Per shift average 2.5 mg 34 mg Amount in 2L drinking water 200 μg 20 μg Per shift average 0.036 mg/kg 0.48 mg/kg 2.9μg/kg 0.29μg/kg ii No-effect level for tests of thyroid function in occupationally exposed Based on a 70-kg adult Exposed in utero via maternal consumption of drinking water iii Model - Human Health and Perchlorate Exposure Ranges Summary I • Thyroid - the critical effect organ of perchlorate toxicity • Perchlorate blocks iodide uptake by NIS • Assuming intake of 2 liters of water per day, the highest known level of ClO4- in public drinking water (24 μg/L) would yield a daily exposure of less than 50 μg/day – 700 times lower than the no effect level Summary II • Absence of an observed effect on neonatal thyroid, thyroidal diseases, or thyroidal cancer in areas with ClO4- in drinking water is epidemiologically consistent with human toxicological and pharmacological observations Summary III • Methods for measurement of ClO4- in urine, serum, solid matrix, and soil will need to be standardized in order to allow a better analysis and interpretation of data