Dopamine transporter availability in alcohol and opioid dependent subjects – a 99mTc-TRODAT-1SPECT imaging and genetic association study

•Dopamine transporter regulates dopamine levels through epigenetic mechanisms.•SPECT/CT revealed significantly reduced DAT availability in AD compared to controls.•Significant increase in DAT promoter methylation in AD compared to controls and OD.•DAT1 promotermethylation in AD significantly associa...

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Published inPsychiatry research. Neuroimaging Vol. 305; p. 111187
Main Authors Grover, Tripti, Gupta, Ranjan, Arora, Geetanjali, Bal, Chandra Shekhar, Ambekar, Atul, Basu Ray, Subrata, Vaswani, Meera, Sharma, Arundhati
Format Journal Article
LanguageEnglish
Published Elsevier B.V 30.11.2020
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ISSN0925-4927
1872-7506
1872-7506
DOI10.1016/j.pscychresns.2020.111187

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Abstract •Dopamine transporter regulates dopamine levels through epigenetic mechanisms.•SPECT/CT revealed significantly reduced DAT availability in AD compared to controls.•Significant increase in DAT promoter methylation in AD compared to controls and OD.•DAT1 promotermethylation in AD significantly associated with lower TRODAT-1 uptake. Drug dependence associated with increased dopamine neurotransmission and neuroplastic changes is influenced by Dopamine transporters (DAT) which are modulated by genetic and epigenetic factors. This study assesses DAT availability in relation to the 40bp DAT1 VNTR (genetic) and DAT1 promoter methylation (epigenetic) changes in patients with alcohol dependence (AD) and opioid dependence (OD). A total of 60 subjects (n=20 each of AD, OD and controls) were recruited. SPECT/CT imaging using 99mTc-TRODAT-1 was performed for measuring striatal DAT availability and DNA screened to check DAT1promoter methylation and 40bp VNTR polymorphism. SPECT/CT imaging revealed significant decrease in DAT availability in the striatum and putamen and significant increase in DAT1 promoter methylation in AD compared to control and OD. The 40bp VNTR distribution was similar in all three groups with 10repeat and 9repeat alleles being the most common. The AD individuals with DAT1promoter methylation showed significantly lower TRODAT-1 uptake compared to the ones with no methylation. AD individuals homozygous for the 10repeat VNTR also showed reduced DAT availability. This is the first imaging study using 99mTc-TRODAT-1 from India documenting significantly reduced striatal DAT availability, increased DAT methylation and frequency of 10repeat individuals associated with decreased DAT availability in AD.
AbstractList •Dopamine transporter regulates dopamine levels through epigenetic mechanisms.•SPECT/CT revealed significantly reduced DAT availability in AD compared to controls.•Significant increase in DAT promoter methylation in AD compared to controls and OD.•DAT1 promotermethylation in AD significantly associated with lower TRODAT-1 uptake. Drug dependence associated with increased dopamine neurotransmission and neuroplastic changes is influenced by Dopamine transporters (DAT) which are modulated by genetic and epigenetic factors. This study assesses DAT availability in relation to the 40bp DAT1 VNTR (genetic) and DAT1 promoter methylation (epigenetic) changes in patients with alcohol dependence (AD) and opioid dependence (OD). A total of 60 subjects (n=20 each of AD, OD and controls) were recruited. SPECT/CT imaging using 99mTc-TRODAT-1 was performed for measuring striatal DAT availability and DNA screened to check DAT1promoter methylation and 40bp VNTR polymorphism. SPECT/CT imaging revealed significant decrease in DAT availability in the striatum and putamen and significant increase in DAT1 promoter methylation in AD compared to control and OD. The 40bp VNTR distribution was similar in all three groups with 10repeat and 9repeat alleles being the most common. The AD individuals with DAT1promoter methylation showed significantly lower TRODAT-1 uptake compared to the ones with no methylation. AD individuals homozygous for the 10repeat VNTR also showed reduced DAT availability. This is the first imaging study using 99mTc-TRODAT-1 from India documenting significantly reduced striatal DAT availability, increased DAT methylation and frequency of 10repeat individuals associated with decreased DAT availability in AD.
Drug dependence associated with increased dopamine neurotransmission and neuroplastic changes is influenced by Dopamine transporters (DAT) which are modulated by genetic and epigenetic factors. This study assesses DAT availability in relation to the 40bp DAT1 VNTR (genetic) and DAT1 promoter methylation (epigenetic) changes in patients with alcohol dependence (AD) and opioid dependence (OD). A total of 60 subjects (n=20 each of AD, OD and controls) were recruited. SPECT/CT imaging using 99mTc-TRODAT-1 was performed for measuring striatal DAT availability and DNA screened to check DAT1promoter methylation and 40bp VNTR polymorphism. SPECT/CT imaging revealed significant decrease in DAT availability in the striatum and putamen and significant increase in DAT1 promoter methylation in AD compared to control and OD. The 40bp VNTR distribution was similar in all three groups with 10repeat and 9repeat alleles being the most common. The AD individuals with DAT1promoter methylation showed significantly lower TRODAT-1 uptake compared to the ones with no methylation. AD individuals homozygous for the 10repeat VNTR also showed reduced DAT availability. This is the first imaging study using 99mTc-TRODAT-1 from India documenting significantly reduced striatal DAT availability, increased DAT methylation and frequency of 10repeat individuals associated with decreased DAT availability in AD.Drug dependence associated with increased dopamine neurotransmission and neuroplastic changes is influenced by Dopamine transporters (DAT) which are modulated by genetic and epigenetic factors. This study assesses DAT availability in relation to the 40bp DAT1 VNTR (genetic) and DAT1 promoter methylation (epigenetic) changes in patients with alcohol dependence (AD) and opioid dependence (OD). A total of 60 subjects (n=20 each of AD, OD and controls) were recruited. SPECT/CT imaging using 99mTc-TRODAT-1 was performed for measuring striatal DAT availability and DNA screened to check DAT1promoter methylation and 40bp VNTR polymorphism. SPECT/CT imaging revealed significant decrease in DAT availability in the striatum and putamen and significant increase in DAT1 promoter methylation in AD compared to control and OD. The 40bp VNTR distribution was similar in all three groups with 10repeat and 9repeat alleles being the most common. The AD individuals with DAT1promoter methylation showed significantly lower TRODAT-1 uptake compared to the ones with no methylation. AD individuals homozygous for the 10repeat VNTR also showed reduced DAT availability. This is the first imaging study using 99mTc-TRODAT-1 from India documenting significantly reduced striatal DAT availability, increased DAT methylation and frequency of 10repeat individuals associated with decreased DAT availability in AD.
ArticleNumber 111187
Author Arora, Geetanjali
Bal, Chandra Shekhar
Sharma, Arundhati
Ambekar, Atul
Gupta, Ranjan
Grover, Tripti
Basu Ray, Subrata
Vaswani, Meera
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  organization: Laboratory of Cyto-Molecular Genetics, Department of Anatomy, AIIMS, New Delhi 110029, India
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Keywords Opioid
Epigenetics
Alcohol
Dopamine transporter
DAT1, VNTR
SPECT
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SSID ssj0023863
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Snippet •Dopamine transporter regulates dopamine levels through epigenetic mechanisms.•SPECT/CT revealed significantly reduced DAT availability in AD compared to...
Drug dependence associated with increased dopamine neurotransmission and neuroplastic changes is influenced by Dopamine transporters (DAT) which are modulated...
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elsevier
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 111187
SubjectTerms Alcohol
DAT1, VNTR
Dopamine transporter
Epigenetics
Opioid
SPECT
Title Dopamine transporter availability in alcohol and opioid dependent subjects – a 99mTc-TRODAT-1SPECT imaging and genetic association study
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0925492720301591
https://dx.doi.org/10.1016/j.pscychresns.2020.111187
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Volume 305
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