Validation of Norepinephrine Transporter (NET) mRNA as a Measure of Functional NET Expression in Postural Tachycardia Syndrome (POTS)
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 200
- 试验地点
- 1
- 主要终点
- Supine Plasma DHPG:NE correlation
研究概览
简要总结
DNA Acetylation can be responsible for significant down-regulation of transcription of the Norepinephrine Transporter (NET). NET is an important clearance transporter that removes norepinephrine (NE) from sympathetic neuronal synapses. Very low levels of NET can "cause" Postural Tachycardia Syndrome (POTS) or make these patients more susceptible to certain medications. Quantified NET messenger RNA (mRNA) levels from a peripheral blood sample may be able to assess NET availability, which is simpler than older methods. This has not been validated against NET function. In this protocol, the investigators seek to assess whether these NET mRNA levels correlate with NET function. The investigators will assess the DHPG (NET dependent NE metabolite):NE ratio in POTS patients and control subjects from both plasma and urine samples.
详细描述
Work from The Baker Institute in Melbourne, Australia has shown that there can be significant epigenetic modification of the Norepinephrine Transporter (NET). DNA Acetylation can be responsible for significant down-regulation of transcription. NET is an important clearance transporter that removes norepinephrine (NE) from sympathetic neuronal synapses.Very low levels of NET can produce a hyperadrenergic phenotype and can "cause" Postural Tachycardia Syndrome (POTS). The Baker Institute researchers have started using quantified NET mRNA levels from a peripheral blood sample to assess NET availability. This is a huge advance due to its simplicity, in contrast to a prior method which involved a vein biopsy to look at the level of protein expression.
In this protocol, the investigators seek to assess whether these NET messenger RNA (mRNA) levels correlate with NET function. When NET transports NE back into presynaptic neurons, a high percentage gets converted to a metabolite (DHPG) and then released into the blood stream. Therefore, the ratio of DHPG:NE ratio is decreased with reduced NET activity. The investigators will assess this DHPG:NE ratio in POTS patients and control subjects from both plasma and urine samples.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 13 Years 至 80 Years(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •• Postural Tachycardia Syndrome
- •Previously diagnosed with POTS
- •Control Subjects
- •Not diagnosed with POTS
- •Age between 13-80 years
- •Male and female subjects are eligible.
- •Able and willing to provide informed consent (if ≥18 years) or assent with parental consent (if age 13-17 years)
排除标准
- •• Inability to give, or withdrawal of, informed consent
- •Use of serotonin-norepinephrine reuptake inhibitors (SNRI) or NET inhibitors within 1 month
- •o These drugs pharmacologically block NET activity
- •Use of Tricyclic antidepressants within 1 week
- •o Many tricyclic antidepressants pharmacologically block NET activity
- •Other factors which in the investigator's opinion would prevent the subject from completing the protocol.
结局指标
主要结局
Supine Plasma DHPG:NE correlation
时间窗: 1 day
NET mRNA above and below median supine plasma DHPG:NE
次要结局
- Standing Plasma DHPG:NE correlation(1 day)
- Urine DHPG:NE correlation(1 day)
研究者
Satish R. Raj
Adjunct Associate Professor of Medicine
Vanderbilt University Medical Center
