• Sign Up

Pramipexole


Pramipexole

Article Author:
Raman Singh
Article Editor:
Mayur Parmar
Updated:
5/30/2020 8:47:55 PM
For CME on this topic:
Pramipexole CME
PubMed Link:
Pramipexole

Indications

Dopaminergic agonists have been used for the treatment of Parkinsonism. They can categorize into ergot derived and non-ergot derived. The focus of this review is pramipexole; a non-ergot derived dopaminergic agonist used broadly in the treatment of Parkinson’s disease (PD) and restless leg syndrome (RLS). The FDA approved pramipexole for treatment of PD in 1997 as monotherapy or add-on drug to other first-line agents.[1] Younger patients are more prone to the motor fluctuations seen in patients treated with levodopa-carbidopa, the most effective agent in treating PD. Hence, treatment with pramipexole should initiate as monotherapy in young patients with PD. On the other hand, elderly patients are more susceptible to the adverse effects of pramipexole-it should only be used when there are motor fluctuations with levodopa-carbidopa therapy. Using pramipexole can permit levodopa-carbidopa dose reduction, thus help overcome the “off” periods seen.[2]

Two years later, the first randomized control trial was conducted on pramipexole to explore its efficacy in treating RLS. After several studies in this regard, the FDA approved pramipexole for the treatment of RLS in 2006, shortly after it approved ropinirole in 2005, another drug of the same group. [3]Apart from the FDA approved indications, studies have shown that pramipexole has been effective in the treatment of bipolar depression and treatment-resistant depression.[4] Besides, a study yielded promising results regarding the efficacy of pramipexole in essential tremors.[5] However, all the studies, though promising, suggested that further trials are necessary to prove the efficacy of pramipexole in the above conditions.

Pramipexole’s role has also been discovered in patients chronically treated with morphine. A very recent study suggested that it has been effective in reducing tolerance to morphine and shortening the duration of its withdrawal symptoms. This result led to the conclusion that pramipexole could restore the analgesic effects of morphine in a patient once they weaned off it.[6]

Mechanism of Action

Pramipexole is a selective dopaminergic agonist with a minor agonistic activity at other receptors. According to the dissociation constant (Km in nmol/L), the lower the value, the higher affinity of a drug to a receptor. Pramipexole recorded the lowest Km value with the D3 dopaminergic receptor and a slightly higher value for the D2 receptor. Therefore, pramipexole is highly specific to D3 and D2 receptors with affinity to D3 being about eight times higher than that to D2. Affinity to D1 receptors is insignificant, being around 200000 times lower than that to D3. Apart from dopaminergic activity, pramipexole exhibits a small affinity to some serotonergic and adrenergic receptors.[3]

Pramipexole’s efficacy in PD is attributed to its D3 selectivity. It binds to presynaptic dopamine autoreceptors exerting negative feedback on endogenous dopamine synthesis. This process leads to a decrease in oxidative stress, which mitigates the damage on the nigrostriatal pathways.[7]

Although the exact pathophysiology of RLS has remained undiscovered, studies strongly suggest a dopaminergic involvement. Unlike in PD, where the nigrostriatal pathways are affected, a set of neurons in the midbrain appears to be the target in RLS. These neurons project into the dorsal horn of the spinal cord modulating nociception. Pramipexole, given to RLS patients, restores optimal neurotransmission in these pathways.[8]

Pramipexole exerts an anti-depressant effect in PD and cases of major depressive disorder. Studies show that such patients have downregulation of dopaminergic receptors, increasing their suicidal propensity. Pramipexole plays a role in the upregulation of such receptors and their potentiation in the mesolimbic system, an area of the brain responsible for mood regulation.[9][10]

Administration

Pramipexole is administered orally and is available in the form of tablets. As soon as it got approved for the treatment of PD, the immediate release (IR) tablet form became available in doses of 0.125, 0.25, 0.5, 1, and 1.5 mg. In 2010, pramipexole became available in the form of extended-release (ER) in larger doses of 0.375, 0.75, 1.5, 2.25, 3, 3.75, and 4.5 mg,  permitting a simplified single daily dosing. Both IR and ER have an identical mechanism of action and efficacy.[11] For instance, 4.5 mg ER administered once daily is clinically equivalent to 1.5 mg IR administered three times daily.[12]

In PD, pramipexole is initiated at a dose of 0.125 mg thrice daily and gradually increased every week to a maximum dose of 1.5 mg thrice daily, depending on the clinical response. This slow titration is to minimize the adverse effects of the drug.[3] In patients with renal insufficiency, pramipexole has to be titrated according to the degree of the insufficiency, as it is almost entirely excreted unchanged through the kidneys. In patients with creatinine clearance (CrCL) of 35-59 ml/min, the initial dose administered should be 0.125 mg twice daily and increased gradually over a longer period of two weeks as compared to a week in patients with normal renal function. For severe renal impairment (CrCL of 15-34 ml/min), the initial dose should be 0.125 once daily.[8][12]

Pramipexole is given as a single dose 2 to 3 hours before bedtime for the treatment of RLS. The dose can be increased every 4 to 7 days to attain maximum symptom relief. Usually, most of the patients are free of symptoms in the dose range of 0.125 and 0.75 mg. Hence, IR tablets are most suitable in RLS, given the small dose required for symptoms to abate.[8]

No dose adjustments should be made in cases of hepatic insufficiency since pramipexole undergoes minimal hepatic metabolism.[13]

Adverse Effects

The adverse effects of pramipexole are attributed to both peripheral and central dopaminergic stimulation. These include in decreasing order of frequency, dyskinesia, postural dizziness, nausea, orthostatic hypotension, and visual hallucinations. Other infrequent ones include fatigue, headache, and constipation.

A severe adverse effect is the sudden onset of sleep, which can lead to road traffic accidents. Consequently, manufacturers issued a warning concerning the use of pramipexole in patients involved in driving or activities demanding vigilance.[13]

Compulsive behaviors like punding and impulse control disorders like gambling, excessive shopping, and hypersexuality are known, serious adverse effects of treatment with pramipexole.[2]

Contraindications

Renal impairment is not a contraindication to pramipexole use. In geriatric patients with declining renal function and younger ones with renal insufficiency, the dose requires titration at a much slower rate. Hepatic insufficiency is not a contraindication as well.[2][13]

Pregnancy may be a contraindication to pramipexole use. Studies conducted on rats showed that pramipexole could affect fetal development at higher doses. The evidence of teratogenicity remains insufficient. Hence, the advice is to avoid pramipexole in pregnancy. Being a dopaminergic agonist, it is contraindicated in lactating mothers since it suppresses lactation. Moreover, it is around six times more concentrated in milk than in plasma - the risk of transmission to the nursing baby increases.[8]

As mentioned earlier, pramipexole causes sudden sleep attacks in individuals. Hence, drivers or people who have jobs requiring alertness are advised against the use of the drug.[13]

Monitoring

The therapeutic plasma concentration of pramipexole is around 0.2 to 7 ng/ml.[14] According to a study, most PD patients who were in remission had a plasma concentration of 2.47 +/- 3.27 ng/mL.[15] This concentration should be cautiously monitored in patients with renal impairment to prevent pramipexole toxicity. The elimination half-life of 8 to 12 hours in individuals with normal renal function increases to 36 hours in patients with moderate to severe renal function.[15]

Toxicity

There has been little evidence of pramipexole toxicity due to overdose. A case report has been published in the literature describing attempted suicide with a variety of medications. However, the overdose manifestations were more suggestive of pramipexole toxicity more than that of other drugs. A 59-year-old male was brought to the hospital 5 hours after ingesting 3 mg pramipexole, 2250 mg venlafaxine SR, and 360 mg mirtazapine.

His vitals were stable, and his neurological examination, including muscle tone and power, was normal. He was mildly agitated and had visual hallucinations. Nine hours later, he developed severe myoclonus to the extent he feared falling from bed. He consistently reported spiders crawling in the room and an alien man sitting on a chair next to him. He had some degree of urinary retention and was jittery and hypervigilant and could not move due to postural dizziness. His routine blood reports were normal, with mild elevation in lactate. The serum concentration of pramipexole was significantly elevated at 34.2 ng/ml, around five times the upper limit of the therapeutic range. It decreased progressively, and the patient was then discharged after his symptoms subsided.

The combination of the above symptoms was very suggestive of pramipexole toxicity. The patient did not meet the Hunter Serotonin Toxicity Criteria, which rules out venlafaxine toxicity. Moreover, mirtazapine overdose is known to cause hypersomnolence.

The patient received no specific antidote. Only 5 mg diazepam was given to control his agitation.[14]

Enhancing Healthcare Team Outcomes

To improve treatment outcomes in PD patients, the role of transdermal administration of dopamine agonists (DA) has been under investigation. In many patients, switching from oral DA such as pramipexole to transdermal DA such as rotigotine proved to be beneficial. These include ones with swallowing difficulties and gastrointestinal symptoms. Gastroparesis significantly reduces the absorption of oral PD, minimizing its therapeutic benefit. Transdermal rotigotine bypasses GI reducing the incidence of nausea and vomiting and obviating the problem of absorption due to gastroparesis. Transdermal patches are an effective alternative in patients on pramipexole undergoing surgery. Many patients have switched to rotigotine before surgery and restarted pramipexole post-operatively. Neurologists and anesthesiologists agree that the transdermal route can be as effective as oral DA in controlling PD symptoms preoperatively.

In patients with renal impairment, transdermal rotigotine can be used instead of pramipexole and other renally excreted oral DA.

Evidence suggests that the route of administration and formulation of the DA influences the occurrence of impulse control disorder (ICD). Studies show that the incidence of ICD in patients treated with transdermal rotigotine is lower than that in patients treated with oral PD agents like pramipexole. ICDs are attributed to the D3 selectivity of oral DA. Rotigotine being less selective to D3 poses a smaller risk of ICD.[16]

Pramipexole is well known to improve depressive symptoms in patients with PD through direct dopaminergic stimulation. Its efficacy has recently had investigative activity in cases of bipolar depression and treatment-resistant depression (TRD). A case report from France suggested that a combination of selegiline and pramipexole was effective in the treatment of TRD. One study indicated that pramipexole could be effective in treating depression resistant to electroconvulsive therapy. More studies are necessary in this regard. However, such promising results can offer a few more options for healthcare professionals to treat depression resistant to first-line agents.[17][4]


References

[1] Pramipexole 2012;     [PubMed PMID: 31643301]
[2] Chen JJ,Swope DM, Pharmacotherapy for Parkinson's disease. Pharmacotherapy. 2007 Dec;     [PubMed PMID: 18041936]
[3] Varga LI,Ako-Agugua N,Colasante J,Hertweck L,Houser T,Smith J,Watty AA,Nagar S,Raffa RB, Critical review of ropinirole and pramipexole - putative dopamine D(3)-receptor selective agonists - for the treatment of RLS. Journal of clinical pharmacy and therapeutics. 2009 Oct;     [PubMed PMID: 19744006]
[4] Moirand R,Galvao F,Dondé C, Pramipexole and Selegiline Combination Therapy in a Case of Treatment-Resistant Depression. Journal of clinical psychopharmacology. 2019 Nov/Dec;     [PubMed PMID: 31688405]
[5] Herceg M,Nagy F,Pál E,Janszky J,Késmárky I,Komoly S,Kovács N, Pramipexole may be an effective treatment option in essential tremor. Clinical neuropharmacology. 2012 Mar-Apr;     [PubMed PMID: 22318193]
[6] Rodgers HM,Lim SA,Yow J,Dinkins ML,Patton R,Clemens S,Brewer KL, Dopamine D{sub}1{/sub} or D{sub}3{/sub} receptor modulators prevent morphine tolerance and reduce opioid withdrawal symptoms. Pharmacology, biochemistry, and behavior. 2020 Apr 23;     [PubMed PMID: 32335101]
[7] Li PC,Yeh CK,Wang SW, Time-intensity-based volumetric flow measurements: an in vitro study. Ultrasound in medicine     [PubMed PMID: 11978415]
[8] Merlino G,Serafini A,Robiony F,Valente M,Gigli GL, Clinical experience with pramipexole in the treatment of restless legs syndrome. Expert opinion on drug metabolism     [PubMed PMID: 18248314]
[9] Krystal AD, Sleep therapeutics and neuropsychiatric illness. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 2020 Jan;     [PubMed PMID: 31376815]
[10] Singh A,Althoff R,Martineau RJ,Jacobson J, Pramipexole, ropinirole, and mania in Parkinson's disease. The American journal of psychiatry. 2005 Apr;     [PubMed PMID: 15800169]
[11] Xiang W,Sun YQ,Teoh HC, Comparison of nocturnal symptoms in advanced Parkinson's disease patients with sleep disturbances: pramipexole sustained release versus immediate release formulations. Drug design, development and therapy. 2018;     [PubMed PMID: 30013321]
[12] Frampton JE, Pramipexole extended-release: a review of its use in patients with Parkinson's disease. Drugs. 2014 Dec;     [PubMed PMID: 25385556]
[13] Deleu D,Northway MG,Hanssens Y, Clinical pharmacokinetic and pharmacodynamic properties of drugs used in the treatment of Parkinson's disease. Clinical pharmacokinetics. 2002;     [PubMed PMID: 11978145]
[14] Cardon-Dunbar A,Robertson T,Roberts MS,Isbister GK, Pramipexole Overdose Associated with Visual Hallucinations, Agitation and Myoclonus. Journal of medical toxicology : official journal of the American College of Medical Toxicology. 2017 Dec;     [PubMed PMID: 28547577]
[15] Contin M,Lopane G,Mohamed S,Calandra-Buonaura G,Capellari S,De Massis P,Nassetti S,Perrone A,Riva R,Sambati L,Scaglione C,Cortelli P, Clinical pharmacokinetics of pramipexole, ropinirole and rotigotine in patients with Parkinson's disease. Parkinsonism     [PubMed PMID: 30446407]
[16] Chung SJ,Asgharnejad M,Bauer L,Benitez A,Boroojerdi B,Heidbrede T,Little A,Kim HJ, Switching from an oral dopamine receptor agonist to rotigotine transdermal patch: a review of clinical data with a focus on patient perspective. Expert review of neurotherapeutics. 2017 Jul;     [PubMed PMID: 28548894]
[17] Gauthier C,Souaiby L,Advenier-Iakovlev E,Gaillard R, Pramipexole and Electroconvulsive Therapy in Treatment-Resistant Depression. Clinical neuropharmacology. 2017 Nov/Dec;     [PubMed PMID: 29059135]