Increased risk of Parkinson's disease in individuals hospitalized with conditions related to the use of methamphetamine or other amphetamine-type drugs

Abstract Background Since methamphetamine and other amphetamine-type stimulants (meth/amphetamine) can damage dopaminergic neurons, researchers have long speculated that these drugs may predispose users to develop Parkinson's disease (PD), a dopamine deficiency neurological disorder. Methods We...

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Veröffentlicht in:Drug and alcohol dependence 2012-01, Vol.120 (1), p.35-40
Hauptverfasser: Callaghan, Russell C, Cunningham, James K, Sykes, Jenna, Kish, Stephen J
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container_title Drug and alcohol dependence
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creator Callaghan, Russell C
Cunningham, James K
Sykes, Jenna
Kish, Stephen J
description Abstract Background Since methamphetamine and other amphetamine-type stimulants (meth/amphetamine) can damage dopaminergic neurons, researchers have long speculated that these drugs may predispose users to develop Parkinson's disease (PD), a dopamine deficiency neurological disorder. Methods We employed a retrospective population-based cohort study using all linked statewide California inpatient hospital episodes and death records from January 1, 1990 through December 31, 2005. Patients at least 30 years of age were followed for up to 16 years. Competing risks analysis was used to determine whether the meth/amphetamine cohort had elevated risk of developing PD (ICD-9 332.0; ICD-10 G20) in comparison to a matched population-proxy appendicitis group and a matched cocaine drug control group. Individuals admitted to hospital with meth/amphetamine-related conditions ( n = 40,472; ICD-9 codes 304.4, 305.7, 969.7, E854.2) were matched on age, race, sex, date of index admission, and patterns of hospital admission with patients with appendicitis conditions ( n = 207,831; ICD-9 codes 540–542) and also individuals with cocaine-use disorders ( n = 35,335; ICD-9 codes 304.2, 305.6, 968.5). Results The meth/amphetamine cohort showed increased risk of PD compared to both that of the matched appendicitis group [hazard ratio (HR) = 1.76, 95% CI: 1.12–2.75, p = 0.017] and the matched cocaine group [HR = 2.44, 95% CI: 1.32–4.41, p = 0.004]. The cocaine group did not show elevated hazard of PD compared to the matched appendicitis group [HR = 1.04, 95% CI: 0.56–1.93, p = 0.80]. Conclusion These data provide evidence that meth/amphetamine users have above-normal risk for developing PD.
doi_str_mv 10.1016/j.drugalcdep.2011.06.013
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Methods We employed a retrospective population-based cohort study using all linked statewide California inpatient hospital episodes and death records from January 1, 1990 through December 31, 2005. Patients at least 30 years of age were followed for up to 16 years. Competing risks analysis was used to determine whether the meth/amphetamine cohort had elevated risk of developing PD (ICD-9 332.0; ICD-10 G20) in comparison to a matched population-proxy appendicitis group and a matched cocaine drug control group. Individuals admitted to hospital with meth/amphetamine-related conditions ( n = 40,472; ICD-9 codes 304.4, 305.7, 969.7, E854.2) were matched on age, race, sex, date of index admission, and patterns of hospital admission with patients with appendicitis conditions ( n = 207,831; ICD-9 codes 540–542) and also individuals with cocaine-use disorders ( n = 35,335; ICD-9 codes 304.2, 305.6, 968.5). Results The meth/amphetamine cohort showed increased risk of PD compared to both that of the matched appendicitis group [hazard ratio (HR) = 1.76, 95% CI: 1.12–2.75, p = 0.017] and the matched cocaine group [HR = 2.44, 95% CI: 1.32–4.41, p = 0.004]. The cocaine group did not show elevated hazard of PD compared to the matched appendicitis group [HR = 1.04, 95% CI: 0.56–1.93, p = 0.80]. Conclusion These data provide evidence that meth/amphetamine users have above-normal risk for developing PD.</description><identifier>ISSN: 0376-8716</identifier><identifier>EISSN: 1879-0046</identifier><identifier>DOI: 10.1016/j.drugalcdep.2011.06.013</identifier><identifier>PMID: 21794992</identifier><identifier>CODEN: DADEDV</identifier><language>eng</language><publisher>Shannon: Elsevier Ireland Ltd</publisher><subject>Addictive behaviors ; Adult ; Adult and adolescent clinical studies ; Amphetamine ; Amphetamine-Related Disorders - complications ; Amphetamines ; Amphetamines - adverse effects ; Appendicitis ; Appendicitis - complications ; Biological and medical sciences ; Case-Control Studies ; Cocaine ; Cocaine-Related Disorders - complications ; Cohort studies ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Dopamine ; Drug addiction ; Female ; Hospitalization ; Hospitals ; Humans ; Incidence ; Male ; Medical sciences ; Methamphetamine ; Methamphetamine - adverse effects ; Middle Aged ; Movement disorders ; Neurology ; Organic mental disorders. Neuropsychology ; Parkinson Disease, Secondary - chemically induced ; Parkinson's disease ; Propensity Score ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Retrospective Studies ; Risk Factors</subject><ispartof>Drug and alcohol dependence, 2012-01, Vol.120 (1), p.35-40</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2011 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ireland Ltd. 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Methods We employed a retrospective population-based cohort study using all linked statewide California inpatient hospital episodes and death records from January 1, 1990 through December 31, 2005. Patients at least 30 years of age were followed for up to 16 years. Competing risks analysis was used to determine whether the meth/amphetamine cohort had elevated risk of developing PD (ICD-9 332.0; ICD-10 G20) in comparison to a matched population-proxy appendicitis group and a matched cocaine drug control group. Individuals admitted to hospital with meth/amphetamine-related conditions ( n = 40,472; ICD-9 codes 304.4, 305.7, 969.7, E854.2) were matched on age, race, sex, date of index admission, and patterns of hospital admission with patients with appendicitis conditions ( n = 207,831; ICD-9 codes 540–542) and also individuals with cocaine-use disorders ( n = 35,335; ICD-9 codes 304.2, 305.6, 968.5). Results The meth/amphetamine cohort showed increased risk of PD compared to both that of the matched appendicitis group [hazard ratio (HR) = 1.76, 95% CI: 1.12–2.75, p = 0.017] and the matched cocaine group [HR = 2.44, 95% CI: 1.32–4.41, p = 0.004]. The cocaine group did not show elevated hazard of PD compared to the matched appendicitis group [HR = 1.04, 95% CI: 0.56–1.93, p = 0.80]. Conclusion These data provide evidence that meth/amphetamine users have above-normal risk for developing PD.</description><subject>Addictive behaviors</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Amphetamine</subject><subject>Amphetamine-Related Disorders - complications</subject><subject>Amphetamines</subject><subject>Amphetamines - adverse effects</subject><subject>Appendicitis</subject><subject>Appendicitis - complications</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Cocaine</subject><subject>Cocaine-Related Disorders - complications</subject><subject>Cohort studies</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Dopamine</subject><subject>Drug addiction</subject><subject>Female</subject><subject>Hospitalization</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methamphetamine</subject><subject>Methamphetamine - adverse effects</subject><subject>Middle Aged</subject><subject>Movement disorders</subject><subject>Neurology</subject><subject>Organic mental disorders. Neuropsychology</subject><subject>Parkinson Disease, Secondary - chemically induced</subject><subject>Parkinson's disease</subject><subject>Propensity Score</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><issn>0376-8716</issn><issn>1879-0046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkt-K1DAUxoso7rj6CpIbWW86npO0aXMj6OKfhQUF9TpkktTJTNvUJF0ZX8TXNWVGV7xQQyBwzu87J8l3ioIgrBGQP9utTZg_q14bO60pIK6BrwHZnWKFbSNKgIrfLVbAGl62DfKz4kGMO8iLC7hfnFFsRCUEXRXfr0YdrIrWkODinviOvFdh78box4tIjItLkrgxb-NunJlVH8nWx8kl1btvWffVpS3RPqeT82MkwfYq5XjyJG0tmbM8Vx1s2qph2tqkBjfmUCA-pwP5LVimw2TJ8rT4sLjX5U720ek8Lz69fvXx8m15_e7N1eWL61LXlKVSY9Viq6pWGQ3CAO0MMg4bwTa0MYphJRqjBdANR1ZZFNCh2LTYtVQjV4ydFxfHulPwX2Ybkxxc1Lbv1Wj9HKWgdVNBQ_HfJFLORAs0k0__SiKliBXUrM5oe0R18DEG28kpuEGFg0SQi9VyJ2-tlovVErjMVmfp41OXeTNY80v409sMPDkBKmrVd0GN2sVbrmaibhqRuZdHzuZ_vnE2yKidHbU1LlidpPHuf27z_I8iunejy3339mDjzs9hzD5KlJFKkB-W0VwmExGANpyzHxbp41Q</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Callaghan, Russell C</creator><creator>Cunningham, James K</creator><creator>Sykes, Jenna</creator><creator>Kish, Stephen J</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><scope>7QJ</scope></search><sort><creationdate>20120101</creationdate><title>Increased risk of Parkinson's disease in individuals hospitalized with conditions related to the use of methamphetamine or other amphetamine-type drugs</title><author>Callaghan, Russell C ; Cunningham, James K ; Sykes, Jenna ; Kish, Stephen J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-c14818a48adc09d02fd1360b93b27da31497dc902b6134e190f19b81f82c16a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Addictive behaviors</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Amphetamine</topic><topic>Amphetamine-Related Disorders - complications</topic><topic>Amphetamines</topic><topic>Amphetamines - adverse effects</topic><topic>Appendicitis</topic><topic>Appendicitis - complications</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Cocaine</topic><topic>Cocaine-Related Disorders - complications</topic><topic>Cohort studies</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>Dopamine</topic><topic>Drug addiction</topic><topic>Female</topic><topic>Hospitalization</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methamphetamine</topic><topic>Methamphetamine - adverse effects</topic><topic>Middle Aged</topic><topic>Movement disorders</topic><topic>Neurology</topic><topic>Organic mental disorders. Neuropsychology</topic><topic>Parkinson Disease, Secondary - chemically induced</topic><topic>Parkinson's disease</topic><topic>Propensity Score</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Callaghan, Russell C</creatorcontrib><creatorcontrib>Cunningham, James K</creatorcontrib><creatorcontrib>Sykes, Jenna</creatorcontrib><creatorcontrib>Kish, Stephen J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Drug and alcohol dependence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Callaghan, Russell C</au><au>Cunningham, James K</au><au>Sykes, Jenna</au><au>Kish, Stephen J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased risk of Parkinson's disease in individuals hospitalized with conditions related to the use of methamphetamine or other amphetamine-type drugs</atitle><jtitle>Drug and alcohol dependence</jtitle><addtitle>Drug Alcohol Depend</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>120</volume><issue>1</issue><spage>35</spage><epage>40</epage><pages>35-40</pages><issn>0376-8716</issn><eissn>1879-0046</eissn><coden>DADEDV</coden><abstract>Abstract Background Since methamphetamine and other amphetamine-type stimulants (meth/amphetamine) can damage dopaminergic neurons, researchers have long speculated that these drugs may predispose users to develop Parkinson's disease (PD), a dopamine deficiency neurological disorder. Methods We employed a retrospective population-based cohort study using all linked statewide California inpatient hospital episodes and death records from January 1, 1990 through December 31, 2005. Patients at least 30 years of age were followed for up to 16 years. Competing risks analysis was used to determine whether the meth/amphetamine cohort had elevated risk of developing PD (ICD-9 332.0; ICD-10 G20) in comparison to a matched population-proxy appendicitis group and a matched cocaine drug control group. Individuals admitted to hospital with meth/amphetamine-related conditions ( n = 40,472; ICD-9 codes 304.4, 305.7, 969.7, E854.2) were matched on age, race, sex, date of index admission, and patterns of hospital admission with patients with appendicitis conditions ( n = 207,831; ICD-9 codes 540–542) and also individuals with cocaine-use disorders ( n = 35,335; ICD-9 codes 304.2, 305.6, 968.5). Results The meth/amphetamine cohort showed increased risk of PD compared to both that of the matched appendicitis group [hazard ratio (HR) = 1.76, 95% CI: 1.12–2.75, p = 0.017] and the matched cocaine group [HR = 2.44, 95% CI: 1.32–4.41, p = 0.004]. The cocaine group did not show elevated hazard of PD compared to the matched appendicitis group [HR = 1.04, 95% CI: 0.56–1.93, p = 0.80]. Conclusion These data provide evidence that meth/amphetamine users have above-normal risk for developing PD.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>21794992</pmid><doi>10.1016/j.drugalcdep.2011.06.013</doi><tpages>6</tpages></addata></record>
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subjects Addictive behaviors
Adult
Adult and adolescent clinical studies
Amphetamine
Amphetamine-Related Disorders - complications
Amphetamines
Amphetamines - adverse effects
Appendicitis
Appendicitis - complications
Biological and medical sciences
Case-Control Studies
Cocaine
Cocaine-Related Disorders - complications
Cohort studies
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Dopamine
Drug addiction
Female
Hospitalization
Hospitals
Humans
Incidence
Male
Medical sciences
Methamphetamine
Methamphetamine - adverse effects
Middle Aged
Movement disorders
Neurology
Organic mental disorders. Neuropsychology
Parkinson Disease, Secondary - chemically induced
Parkinson's disease
Propensity Score
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Retrospective Studies
Risk Factors
title Increased risk of Parkinson's disease in individuals hospitalized with conditions related to the use of methamphetamine or other amphetamine-type drugs
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