full-text:
Acute Kidney Injury Associated with Synthetic Cannabinoid Use — Multiple States, 2012

	MMWR Weekly Volume 62, No. 6 February 15, 2013

Acute Kidney Injury Associated with Synthetic Cannabinoid Use — Multiple States, 2012

Weekly

February 15, 2013 / 62(06);93-98

In March 2012, the Wyoming Department of Health was notified by Natrona County public health officials regarding three patients hospitalized for unexplained acute kidney injury (AKI), all of whom reported recent use of synthetic cannabinoids (SCs), sometimes referred to as "synthetic marijuana." SCs are designer drugs of abuse typically dissolved in a solvent, applied to dried plant material, and smoked as an alternative to marijuana. AKI has not been reported previously in users of SCs and might be associated with 1) a previously unrecognized toxicity, 2) a contaminant or a known nephrotoxin present in a single batch of drug, or 3) a new SC compound entering the market. After the Wyoming Department of Health launched an investigation and issued an alert, a total of 16 cases of AKI after SC use were reported in six states. Review of medical records, follow-up interviews with several patients, and laboratory analysis of product samples and clinical specimens were performed. The results of the investigation determined that no single SC brand or compound explained all 16 cases. Toxicologic analysis of product samples and clinical specimens (available from seven cases) identified a fluorinated SC previously unreported in synthetic marijuana products: (1-(5-fluoropentyl)-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl) methanone, also known as XLR-11, in four of five product samples and four of six patients' clinical specimens. Public health practitioners, poison center staff members, and clinicians should be aware of the potential for renal or other unusual toxicities in users of SC products and should ask about SC use in cases of unexplained AKI.
Epidemiologic Findings
The first three patients (Table 1, cases 1–3) reported smoking SCs in the days or hours before symptom onset. Public health staff members interviewed the three and reviewed their medical records. The patients were young, previously healthy males who reported smoking either a blueberry-flavored SC product (one patient) or an unspecified SC product (two patients). They experienced severe nausea, vomiting, and flank or abdominal pain and went to emergency departments during February 26–29. Local law enforcement officials were notified and released a media advisory warning of illness associated with SC use.
The Wyoming Department of Health launched an investigation to identify other cases and determine the cause of illness. A case initially was defined as nausea, vomiting, abdominal or back pain, and AKI (i.e., serum creatinine concentration above the facility's reference range) in a patient reporting SC use and illness onset during February 1–March 1. Hospital staff members from two regional medical facilities conducted retrospective reviews of emergency department and hospital admission records. The Wyoming Department of Health issued a health alert on March 1 to all licensed health-care providers, hospitals, emergency departments, and urgent-care centers in Wyoming, describing the possible association between AKI and SC use and requesting that potential cases be reported. On March 21, the Wyoming state epidemiologist contacted CDC regarding the first three cases. On March 24, a fourth Wyoming patient became ill after smoking either a blueberry-flavored or bubblegum-flavored SC product and was found to meet the case definition (Table 1, case 4).
A collaboration among several state public health officials, poison center toxicologists, forensic laboratory scientists, individual clinicians, and the Arkansas K2 Research Consortium, identified an additional 12 cases of SC-associated AKI in Oregon (six cases), New York (two), Oklahoma (two), Rhode Island (one), and Kansas (one) in hospitalized patients who had serum creatinine concentration above the facility's reference range after smoking an SC product during March 16–December 3. CDC medical toxicologists reviewed clinical and laboratory data from all 16 cases (Table 1).
All 16 patients initially visited emergency departments and subsequently were hospitalized. The 16 patients included 15 males aged 15–33 years (median: 18.5 years) and one female aged 15 years; all but one had nausea and vomiting. Twelve patients reported abdominal, flank, and/or back pain. None reported preexisting renal dysfunction or use of medication that might have caused renal problems. The highest serum creatinine concentrations (creatinine peak) among the 16 patients ranged from 3.3 to 21.0 mg/dL (median: 6.7 mg/dL; normal 0.6–1.3 mg/dL) and occurred 1–6 days after symptom onset (median: 3 days). Urinalysis for 15 patients showed variable results: proteinuria (eight patients), casts (five), white blood cells (nine), and red blood cells (eight). Twelve patients underwent renal ultrasonograpy, nine of whom had a nonspecific increase in renal cortical echogenicity; none had hydronephrosis.
Six of eight patients with a renal biopsy demonstrated acute tubular injury, and three of eight patients demonstrated features of acute interstitial nephritis. Kidney function recovery was apparent within 3 days of creatinine peak in most patients. However, five of the 16 patients required hemodialysis, and four patients received corticosteroids; none died. Other infectious, autoimmune, pharmacologic, or other toxic causes of AKI were not found.
Toxicologic Analysis
Of the 16 cases, toxicologic analysis of implicated SC products and clinical specimens was possible in seven (Table 2). No single SC product explained all of the cases. Two SC products recovered by law enforcement officials in Wyoming and epidemiologically linked to cases 1–3 were tested by the Arkansas K2 Research Consortium laboratory (Arkansas K2) and the University of California–San Francisco Clinical and Environmental Toxicology Laboratory (UCSF). Gas chromatography/mass spectrometry (Arkansas K2) and liquid chromatography/time-of-flight mass spectrometry (UCSF) analysis revealed that both products contained 3-(1-naphthoyl) indole, a precursor to several aminoalkylindole synthetic cannabinoids. One of the two product samples also contained the potent synthetic cannabinoid AM2201, which has been linked to human disease and death, but not to AKI.
Standardized liquid chromatography–time of flight mass spectrometry methods validated for trace level analysis of synthetic cannabinoid parent compounds and metabolites were used for all clinical assays (UCSF). A sample of the product smoked by the patient in case 4 contained 3-(1-naphthoyl) indole and XLR-11, a previously undescribed fluorinated-derivative of the SC compound UR-144 currently in circulation. A urine specimen collected from the same patient was positive for the XLR-11 N-pentanoic acid metabolite. A blood specimen from the patient in case 6, who smoked "Phantom Wicked Dreams," contained the N-pentanoic acid metabolite of XLR-11. In case 11, analysis of the SC product "Mr. Happy" and a serum specimen revealed the SCs XLR-11 and UR-144; a urine specimen contained the N-pentanoic acid metabolite of XLR-11. In case 12, samples of "Clown Loyal" were found to contain XLR-11. In cases 13 and 14, analysis of "Lava" and associated clinical specimens identified XLR-11 and the N-pentanoic acid metabolite of XLR-11. In case 15, analysis of "Flame 2.0" was negative for XLR-11. For nine of the 16 cases, neither product samples nor clinical specimens were available for analysis.

Reported by

Tracy D. Murphy, MD, Kelly N. Weidenbach, MPH, Clay Van Houten, MS, Wyoming Dept of Health. Roy R. Gerona, PhD, Dept of Laboratory Medicine, Univ of California–San Francisco. Jeffery H. Moran, PhD, Arkansas Public Health Laboratory, Arkansas Dept of Health. Ronald I. Kirschner, MD, Nebraska Regional Poison Center. Jeanna M. Marraffa, PharmD, Christine M. Stork, PharmD, Upstate Medical Univ, Upstate New York Poison Center; Guthrie S. Birkhead, MD, Andie Newman, DVM, New York State Dept of Health. Robert G. Hendrickson, MD, B. Zane Horowitz, MD, Oregon Poison Center; Karen Vian, Douglas County Public Health; Richard F. Leman, MD, Oregon Public Health Div. Stephen L. Thornton, MD, Univ of Kansas Hospital Poison Control Center; Clayton Wood, DO, Dept of Emergency Medicine, Univ of Kansas Hospital. David A. Myers, MD, Oklahoma Univ Health Sciences Center. Erik Orr, MS, Geospatial Research, Analysis, and Services Program, John J. Devlin, MD, Michael D. Schwartz, MD, Office of Environmental Health Emergencies, National Center for Environmental Health; Genevieve L. Buser, MD, EIS Officer, CDC. Corresponding contributor: Michael D. Schwartz, mschwartz@cdc.gov, 770-488-7282.

Editorial Note

Synthetic cannabinoid compounds originally were developed to facilitate study of cannabinoid receptor pharmacology, but in recent years have emerged as drugs of abuse. In 2005, SC products marketed as "Spice" first emerged in European countries, before appearing in the United States in 2009, where they were marketed initially as "K2." Today, SC products are distributed worldwide under countless trade names and packaged in colorful wrappers designed to appeal to teens, young adults, and first-time drug users (1). Products often are packaged with disingenuous labels such as "not for human consumption" or "incense," but health professionals and legal authorities are keenly aware that these products are smoked like marijuana. Despite federal and state regulations to prohibit SC sale and distribution, illicit use continues, and reports of illness are increasing (1–4).
The expectation of a more intense high than that induced by marijuana, easy access, affordability, and avoidance of detection by many commonly used urine drug tests all contribute to the growing abuse of SCs, especially among male adolescents (1,5). The increasing use of SCs by young persons, coupled with mounting evidence of adverse health effects, has led to state and federal legislation (3,6). However, full recognition of the potential dangers of SCs is not widespread among users or sellers, and SC products remain available on the Internet and at many convenience stores. Further, differences in state drug enforcement statutes have led to different laws and approaches to drug enforcement (7).
Although related to delta-9-tetrahydrocannabinol, the active ingredient in marijuana, SCs are two to three times more likely to be associated with sympathomimetic effects (i.e., tachycardia and hypertension), and approximately five times more likely to be associated with hallucinations (8). In addition, an increase in the occurrence of seizures has been reported with SC use (9). This report describes unanticipated AKI with SC abuse. Given the rapidity with which new SC compounds enter the marketplace and their increasing use in the past 3 years, outbreaks of unexpected toxicity associated with their use are likely to increase.
Management of suspected SC toxicity is symptomatic and supportive; no antidote exists. All of the patients in this report recovered creatinine clearance during their hospital stay, although the length of time was variable; one patient was discharged before his creatinine normalized. However, a risk for long-term kidney sequelae might exist. Recent studies suggest an increased risk for chronic and end-stage renal disease following AKI of various etiologies, despite initial recovery (10). Physicians caring for otherwise healthy adolescents and young adults with unexplained AKI should inquire about SC use, and cases of suspected SC poisoning should be reported to both the regional poison center and the appropriate state health department. Regional poison centers can be reached by telephone at 1-800-222-1222, from anywhere in the United States.
In this report, the product used by five of the 16 patients, including two patients (cases 13 and 14) who used the same product, contained a novel fluorinated SC (XLR-11). In addition, XLR-11 and/or XLR-11 metabolites were found in five of the seven cases for whom clinical specimens were available. XLR-11 emerged on the SC market in the first half of 2012; therefore, experience with this fluorinated compound has been limited. The consistent finding of XLR-11 in product samples and clinical specimens has alternative explanations. XLR-11, a metabolite, or a contaminant associated with it might be responsible for AKI in these patients, or its presence might simply reflect the widespread use of this particular compound in SC products during the study period rather than a causal association with AKI. Health-care providers should be aware of renal and other unexpected toxicities from use of SC products, especially with newer SC compounds.

Acknowledgments

Casper-Natrona County Health Dept, Casper Police Dept, Casper, Wyoming. Cindy Moran, Arkansas State Crime Laboratory, Little Rock, Arkansas. Saurabh Dasgupta, MD, Oklahoma Univ Health Sciences Center, Oklahoma City, Oklahoma. Colin Segovich, MD, Miriam Hospital, Providence, Rhode Island.

References

1. Fattore L, Fratta W. Beyond THC: the new generation of cannabinoid designer drugs. Front Behav Neurosci 2011;5:60.
2. Cohen J, Morrison S, Greenberg J, Saidinejad M. Clinical presentation of intoxication due to synthetic cannabinoids. Pediatrics 2012;129:e1064–7.
3. Lapoint J, James LP, Moran CL, Nelson LS, Hoffman RS, Moran JH. Severe toxicity following synthetic cannabinoid ingestion. Clin Toxicol (Phila) 2011;49:760–4.
4. Shanks KG, Dahn T, Terrell AR. Detection of JWH-018 and JWH-073 by UPLC-MS-MS in postmortem whole blood casework. J Anal Toxicol 2012;36:145–52.
5. Bebarta VS, Ramirez S, Varney SM. Spice: a new "legal" herbal mixture abused by young active duty military personnel. Subst Abus 2012;33:191–4.
6. Drug Enforcement Administration. Schedules of controlled substances: temporary placement of five synthetic cannabinoids into schedule I. Washington, DC: US Department of Justice, Drug Enforcement Administration; 2011. Available at http://www.deadiversion.usdoj.gov/fed_regs/rules/2011/fr0301.htm.
7. National Conference of State Legislatures. Synthetic cannabinoids (a.k.a. "K2"/"Spice") enactments. Washington, DC: National Conference of State Legislatures; 2012. Available at http://www.ncsl.org/issues-research/justice/synthetic-cannabinoids-enactments.aspx.
8. Forrester MB, Kleinschmidt K, Schwarz E, Young A. Synthetic cannabinoids and marijuana exposures reported to poison centers. Hum Exp Toxicol 2012;
   31:1006–11.
9. Hoyte CO, Jacob J, Monte AA, Al-Jumaan M, Bronstein AC, Heard K. A characterization of synthetic cannabinoids exposures reported to the National Poison Data System in 2010. Ann Emerg Med 2012;60:435–8.
10. Coca SG, Singanamala S, Parikh CR. Chronic kidney disease after kidney injury: a systemic review and meta-analysis. Kid Int 2012;81:442–8.