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 in | Psychiatry research. Neuroimaging Vol. 305; p. 111187 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
30.11.2020
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ISSN | 0925-4927 1872-7506 1872-7506 |
DOI | 10.1016/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. |
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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 |
Author_xml | – sequence: 1 givenname: Tripti surname: Grover fullname: Grover, Tripti organization: Laboratory of Cyto-Molecular Genetics, Department of Anatomy, AIIMS, New Delhi 110029, India – sequence: 2 givenname: Ranjan surname: Gupta fullname: Gupta, Ranjan organization: Laboratory of Cyto-Molecular Genetics, Department of Anatomy, AIIMS, New Delhi 110029, India – sequence: 3 givenname: Geetanjali surname: Arora fullname: Arora, Geetanjali organization: Department of Nuclear Medicine, AIIMS, New Delhi 110029, India – sequence: 4 givenname: Chandra Shekhar surname: Bal fullname: Bal, Chandra Shekhar organization: Department of Nuclear Medicine, AIIMS, New Delhi 110029, India – sequence: 5 givenname: Atul surname: Ambekar fullname: Ambekar, Atul organization: National Drug Dependence Treatment Center, Department of Psychiatry, AIIMS, New Delhi 110029, India – sequence: 6 givenname: Subrata surname: Basu Ray fullname: Basu Ray, Subrata organization: Laboratory of Cyto-Molecular Genetics, Department of Anatomy, AIIMS, New Delhi 110029, India – sequence: 7 givenname: Meera surname: Vaswani fullname: Vaswani, Meera organization: National Drug Dependence Treatment Center, Department of Psychiatry, AIIMS, New Delhi 110029, India – sequence: 8 givenname: Arundhati surname: Sharma fullname: Sharma, Arundhati email: arundhatisharma1@gmail.com 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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