E Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

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Association of OPRM1 and COMT Single Nucleotide Polymorphisms with Hospital Length of Hospital Stay and Treatment of Neonatal Abstinence Syndrome” E Wachman, M Hayes, M Brown, J Paul, K Harvey- Wilkes, N Terrin, G Huggins, JV Aranda, and JM Davis JAMA Media Briefing April 30, 2013

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“ Association of OPRM1 and COMT Single Nucleotide Polymorphisms with Hospital Length of Hospital Stay and Treatment of Neonatal Abstinence Syndrome”. E Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes, N Terrin , G Huggins, JV Aranda , and JM Davis JAMA Media Briefing April 30, 2013. - PowerPoint PPT Presentation

Transcript of E Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Page 1: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

“Association of OPRM1 and COMT Single Nucleotide Polymorphisms with Hospital Length

of Hospital Stay and Treatment of Neonatal Abstinence Syndrome”

E Wachman, M Hayes, M Brown, J Paul, K Harvey-Wilkes, N Terrin, G Huggins, JV Aranda, and JM Davis

JAMA Media BriefingApril 30, 2013

Page 2: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Disclosures

No Conflicts of Interest

This study was supported in part by NIH funding: DA024806-01A2 to Dr. Marie Hayes

and R01DA032889-01A1 to Dr. Jonathan Davis

Page 3: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Neonatal Abstinence Syndrome

• Opioid exposure in pregnancy - 5.6 infants/1,000 births

• Incidence has tripled in the past decade• The mother may also be smoking or taking

other medications • Signs of withdrawal in 60-80% of infants

exposed to opioids• Dysfunction of the central nervous system,

gastrointestinal tract, and/or respiratory system

Page 4: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Neonatal Abstinence Syndrome

• Prolonged treatment in hospital, high healthcare costs

• Safety and efficacy of agents not well established

• Significant variability in the incidence and severity

• Factors influencing this variability are unknown

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Neonatal Abstinence Syndrome

• Genetic factors may be important

• Single nucleotide polymorphisms (SNPs): Single base pair changes that can alter protein’s function

• SNPs influence opioid dosing, metabolism, and addiction in adults

• No prior studies of genetic links to NAS

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Candidate Genes for NAS• SNPs present in 40-50% of the population have been

studied in adults• Mu Opioid Receptor (OPRM1) = Site of Action

• 118A>G SNP• Multi-Drug Resistance Gene (ABCB1) = Transporter

• 1236C>T SNP• 3435C>T SNP• 2677G/T/A SNP

• Catechol-O-methyltransferase (COMT) = Modulator• 158A>G SNP

Page 7: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Objective• Do SNPs in the OPRM1, ABCB1, and/or COMT

genes influence length of hospital stay (LOS) and need for treatment in infants exposed to opioids during pregnancy

• Outcome Measures: • Primary: Length of hospital stay• Secondary: Treatment for NAS, need for

multiple medications

Page 8: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Methods• 86 opioid exposed term infants• Mothers receiving methadone or buprenorphine• Infants treated with morphine or methadone• If severe - additional medications given• A sample of blood or saliva collected from

each infant • Incidence and severity correlated with changes

in genetic profiles

Page 9: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

ResultsDEMOGRAPHICSWhite 98%

Maternal Methadone 64%

Maternal Buprenorphine 36%

Maternal Smoking 78%

Maternal Benzodiazepines 12%

LOS All Infants Mean 22.3 days

LOS Treated Infants Mean 31.6 days

Treatment for NAS 65%

Treated with >2 medications 24%

Page 10: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

OPRM1 118A>G Results • AA vs AG/GG infants compared in models that

adjust for breastfeeding and study site• Those with the AG/GG genotype - treated less

frequently and had shorter LOS

OUTCOME UNADJUSTEDRESULTS

ADJUSTED RESULTS

P-VALUE

Infant Treated 72% vs 48% OR = 0.76 (CI 0.63, 0.96)

0.006

Mean LOS 24.1 vs 17.6 days - 8.5 days 0.009

Page 11: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

COMT 158A>G Results• AA infants vs AG/GG infants in models that

adjusted for breastfeeding and site• AG/GG infants were treated less frequently and

had shorter LOS than AA infants

OUTCOME UNADJUSTED RESULTS

ADJUSTED RESULTS

P-VALUE

Infant Treated 88% vs 60% OR = 0.79(CI 0.61, 0.99)

0.02

Mean LOS 31.1 vs 20.4 days - 10.8 days 0.005

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Conclusions• NAS is a complex disorder with many factors

contributing to the incidence and severity• SNPs in the OPRM1 and COMT genes - reduced

treatment and LOS• No associations found with ABCB1 SNPs• Combining clinical risk factors with genetic

profiling would permit personalized genetic medicine and targeted treatment regimens

Page 13: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Challenges in Neonatal Drug Development

• Most drugs used in newborn infants not FDA approved - safety and efficacy not established

• Small market, high liability, ethical concerns• Significant variability in NAS treatment protocols• Many NAS medications include alcohol or

propylene glycol • Concern for adverse long-term developmental

outcomes

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Future Directions

• NIH Grant – “Improving Outcomes in Neonatal Abstinence Syndrome”

• Randomize infants to receive morphine or methadone (determine best practice)

• Evaluate long-term neurodevelopmental outcomes of infants treated for NAS

• Establish other genetic factors - Addiction Array (1350 SNPs for addiction disorders)

Page 15: E  Wachman , M Hayes, M Brown, J Paul, K Harvey-Wilkes,

Acknowledgements• The Floating Hospital at Tufts Medical Center:

• Tufts Medical Center, Melrose Wakefield Hospital, Brockton Hospital, and Lowell General Hospital

• Ozlem Kasaroglu, Teresa Marino, Mario Cordova• CTRC Genomics Laboratory

• Eastern Maine Medical Center:• Staff at the EMMC • Hira Shrestha; Nicole Heller, Beth Logan, Deborah

Morrison

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That’s All Folks!