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RLS Atlas

Themensynthese

The Dopamine System in RLS

Was die geprüfte Forschung zu diesem Thema sagt – jede Aussage ist mit einer Studiennotiz, einer PMID und einem Evidenzgrad verknüpft.

Diese Seite fasst die veröffentlichte Evidenz zu The Dopamine System in RLS zusammen: 35 unabhängig geprüfte, evidenzgraduierte Studien, jeweils mit PMID zitiert und von A bis E bewertet.

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This synthesis covers the A11 diencephalospinal pathway, striatal/spinal D1-D3 receptor biology, presynaptic "hyperdopaminergic" signaling, tyrosine hydroxylase and DAT changes, the circadian dopamine rhythm, iron-dopamine interactions, BTBD9/genetic animal models, and dopaminergic drug response as evidence. Every claim below cites a study note filename or PMID. This is a research synthesis, not medical advice; see the standing disclaimer in docs/00_MASTER_PLAN.md (Section 2). Dopamine-agonist withdrawal (DAWS) and augmentation are dangerous when mishandled — any dose change must be physician-supervised and never abrupt.

What is established (grade A/B)

  • Dopaminergic drugs (levodopa and D2/D3 agonists) produce large, statistically robust, and repeatedly replicated reductions in RLS symptom severity and periodic limb movements. This is shown across independent RCTs: pramipexole vs placebo crossover (n=10, PLMS index normalized, p=0.005; 1999-montplaisir-pramipexole-crossover-rct.md), a 344-patient fixed-dose placebo-controlled trial (IRLS change -14.0 to -12.8 vs -9.3 placebo, all p<0.01; 2006-winkelman-pramipexole-fixed-dose-rct.md), a 26-week RCT (IRLS -13.7 vs -11.1, p=0.0077; 2011-hogl-pramipexole-6-month-augmentation-rct.md), cabergoline vs levodopa (n=361; 2007-trenkwalder-cabergoline-levodopa-augmentation.md), and a Cochrane systematic review of 9 levodopa RCTs (n=521), which itself meets grade-A criteria (2011-scholz-cochrane-levodopa-review.md). This drug-response evidence remains the single most robust demonstration that the dopamine system is centrally involved in RLS.
  • Long-term dopamine agonist/levodopa therapy carries a real, quantifiable, dose- and duration-dependent risk of augmentation (paradoxical symptom worsening with earlier onset and spread to other body parts). This is confirmed prospectively in RCTs — 9.2% vs 6.0% at 6 months, rising with duration on pramipexole but not placebo (2011-hogl-pramipexole-6-month-augmentation-rct.md); 9.8% (levodopa) vs 4.0% (cabergoline) at 30 weeks (2007-trenkwalder-cabergoline-levodopa-augmentation.md) — and in a large community cohort (~8%/year for at least 8 years, 20% meeting augmentation criteria; 2011-allen-community-survey-augmentation-incidence.md), matching the master-plan anchor figure of 7-10%/year and the AASM 2024/2025 guideline's conditional recommendation against standard-dose pramipexole/ropinirole/rotigotine (2025-winkelman-aasm-guideline-rls.md).
  • RCT-level "established" efficacy of dopamine agonists is concentrated in the short-to-medium term: the IRLSSG long-term evidence review rates dopamine agonists Level A only up to 6 months, with weaker Level B evidence for 1-5 years (2013-garcia-borreguero-irlssg-long-term-guidelines.md), and the Cochrane review explicitly found that augmentation — "the clinically most relevant adverse event" — was not adequately assessed in the trials it reviewed (2011-scholz-cochrane-levodopa-review.md).

Emerging C

  • In vivo imaging shows real, but inconsistent and sometimes contradictory, dopaminergic abnormalities: reduced striatal D2 binding by PET in drug-naive patients (1999-turjanski-pet-dopamine-d2-binding.md); reduced mesolimbic (nucleus accumbens/caudate) D2/3 binding that predicts treatment response (2012-oboshi-pet-d2d3-treatment-response.md); yet increased striatal DAT density in a separate elderly, drug-naive cohort (2012-kim-dat-spect-elderly-rls.md). Each rests on a single small (n=8-25) case-control study.
  • Circadian neuroendocrine and behavioral testing (small controlled studies, n=7-24) shows dopaminergic reactivity itself varies by time of day: exaggerated nighttime prolactin/growth-hormone response to L-dopa (2004-garcia-borreguero-neuroendocrine-ldopa-circadian.md); rising evening melatonin preceding symptom worsening (2004-michaud-circadian-rhythm-melatonin.md); and immobility-induced discomfort escalating specifically between ~21:20 and 08:00 (2005-michaud-circadian-immobility-symptoms.md).
  • Postmortem tissue shows decreased D2 receptor density (correlating with severity) alongside increased tyrosine hydroxylase in substantia nigra/putamen (2009-connor-dopaminergic-profile-autopsy.md) — the most direct human-tissue evidence for a "presynaptic hyperdopaminergic, postsynaptic hyporesponsive" model, but from a small, comorbidity-laden sample.

Contested or negative findings

  • The direction of striatal DAT change is inconsistent: increased in one elderly cohort (2012-kim-dat-spect-elderly-rls.md) but not significantly different from controls at autopsy (2009-connor-dopaminergic-profile-autopsy.md) — the field has not converged on whether RLS involves DAT up- or down-regulation.
  • Whether RLS is fundamentally "hypodopaminergic" or "hyperdopaminergic" is actively contested: early PET/SPECT work suggested reduced D2 binding (1999-turjanski-pet-dopamine-d2-binding.md), whereas autopsy and adenosine-pathway work argue for a presynaptic hyperdopaminergic state with secondary postsynaptic downregulation (2009-connor-dopaminergic-profile-autopsy.md; 2018-ferre-pivotal-adenosine-neurotransmission.md); a connectome review states outright that "RLS is not simply a hypodopaminergic state" (2016-earley-connectome-dopamine-augmentation-mechanism.md).
  • D3-receptor-centric explanations of augmentation remain hypothesis-level (grade D/E), built on animal models and a single non-powered, 10-subject human pilot trial of the D1 antagonist ecopipam that only "numerically" favored drug over placebo (2025-clemens-d1-d3-receptor-augmentation-model.md; 2017-dinkins-d3-d1-receptor-animal-model.md; 2019-casoni-d3-receptor-agonist-efficacy-review.md) — not yet tested against human augmented-RLS tissue.
  • No animal model reproduces the full subjective human RLS phenotype (2007-ondo-animal-models-rls.md; 2016-allen-animal-models-rls-phenotypes.md), so causal claims built on A11-lesion, D3-knockout, or Btbd9 mice remain inferential for humans.

Mechanistic picture in 5 bullet points

  1. Brain iron insufficiency is the most upstream driver. Iron is a cofactor for tyrosine hydroxylase; deficiency raises TH activity (2009-connor-dopaminergic-profile-autopsy.md), reduces DAT and D2 signaling capacity (2008-bianco-iron-deficiency-dat-levodopa.md), and downregulates adenosine A1 receptors, disinhibiting dopamine/glutamate release (2010-quiroz-adenosine-a2a-iron-deficient-rats.md; 2016-quiroz-adenosine-a1-receptor-downregulation.md; 2018-ferre-pivotal-adenosine-neurotransmission.md).
  2. The A11 diencephalospinal pathway is the near-exclusive source of spinal dopamine, signaling mainly via D2/D3 receptors (2010-barraud-a11-primate-neuroanatomy.md; 2017-ozawa-a11-neuron-subtypes-spinal.md); lesioning it, especially combined with iron deficiency, produces an agonist-reversible RLS-like locomotor phenotype in rodents (2007-zhao-a11-lesion-iron-deprivation-mice.md; 2007-qu-a11-lesion-iron-deprivation-mouse.md).
  3. Symptoms reflect a D1/D3 (excitatory/inhibitory) balance, not simply "too much" or "too little" dopamine. D3-knockout mice show facilitation instead of the normal depression of spinal reflexes and a reversed circadian TH rhythm (2004-clemens-d3-knockout-spinal-reflex.md; 2005-clemens-tyrosine-hydroxylase-circadian-d3ko.md), and GWAS-linked genes (MEIS1, BTBD9, MAP2K5, PTPRD) converge on upregulating D1 receptor expression (2025-clemens-d1-d3-receptor-augmentation-model.md; 2012-deandrade-btbd9-mutant-mice.md; 2009-jellen-systems-genetics-brain-iron.md).
  4. Chronic D3-agonist exposure appears to progressively shift this balance toward D1 dominance via receptor desensitization and D1 upregulation, offering a specific, testable mechanism for augmentation (2023-zeng-augmentation-mechanisms-review.md; 2017-dinkins-d3-d1-receptor-animal-model.md; 2016-earley-connectome-dopamine-augmentation-mechanism.md).
  5. A circadian clock gates dopamine-system symptom expression (evening/night peak), itself linked to melatonin and disrupted in D3-knockout and iron-deficient models and in human neuroendocrine/behavioral testing (2004-michaud-circadian-rhythm-melatonin.md; 2005-michaud-circadian-immobility-symptoms.md; 2004-garcia-borreguero-neuroendocrine-ldopa-circadian.md; 2011-dowling-d3-receptor-iron-deficient-mice.md).

Implications for a non-drug long-term plan for people currently on dopamine agonists or alpha-2-delta ligands

Medical disclaimer: none of this is medical advice. Augmentation and dopamine agonist withdrawal syndrome (DAWS) are dangerous when mishandled — DAWS includes anxiety, panic, dysphoria, depression, agitation, suicidal ideation, and orthostatic hypotension, is refractory to more dopaminergic drug, and currently has no proven effective treatment (2013-nirenberg-dopamine-agonist-withdrawal-review.md). Any change to an existing dopamine agonist or alpha-2-delta ligand regimen must be gradual and physician-supervised, never abrupt or self-directed.

  • Iron correction is the most evidence-supported upstream lever. Because iron deficiency raises TH, lowers DAT/D2 capacity, and downregulates adenosine A1 receptors (mechanistic picture, points 1 and 3), correcting ferritin/transferrin saturation per AASM 2024/2025 thresholds (2025-winkelman-aasm-guideline-rls.md) before or during any dose change is explicitly recommended by the IRLSSG task force to both prevent and treat augmentation (2016-garcia-borreguero-augmentation-prevention-treatment-guidelines.md) and is validated mechanistically in brain-iron-deficiency rodent models (2022-earley-bid-rodent-model-review.md; 2014-earley-iron-dopamine-metabolic-theory-review.md).
  • Time evening/night countermeasures to the circadian vulnerability window. Since dopaminergic/melatonin sensitivity peaks at night (mechanistic picture, point 5), non-drug measures (scheduled evening activity, compression, avoiding exogenous melatonin, consistent sleep-wake timing) are mechanistically best concentrated in the evening-to-early-morning window rather than applied uniformly.
  • Guideline-directed transition toward alpha-2-delta ligands addresses the augmentation mechanism directly. Because augmentation stems from a chronic-agonist-driven D3-to-D1 receptor shift (mechanistic picture, point 4) rather than a fixed, drug-independent process, moving toward alpha-2-delta-ligand-based control (now AASM first-line) removes the specific receptor-level driver; this is the standard guideline "exit ramp" from dopamine agonists (2016-garcia-borreguero-augmentation-prevention-treatment-guidelines.md; 2026-winkelman-rls-jama-clinical-review.md), always via slow, supervised tapering (never abrupt).
  • Watch for and remove aggravating co-medications (serotonergic antidepressants, dopamine antagonists, antihistamines) as part of any tapering plan, per the JAMA review and IRLSSG guidance (2026-winkelman-rls-jama-clinical-review.md; 2016-garcia-borreguero-augmentation-prevention-treatment-guidelines.md).
  • Adenosine-pathway modulation is a promising but still experimental adjunct, not a validated non-drug substitute today (2018-ferre-pivotal-adenosine-neurotransmission.md; 2025-mogavero-adenosine-hypothesis-critical-review.md).
  • Withdrawal itself is not symptom-free, and acute discontinuation of pramipexole, gabapentin, or oxycodone each produce distinct rebound symptom patterns that must be anticipated and managed by a physician during any transition (2018-wang-acute-drug-withdrawal-rls-symptoms.md).

Open questions

  • Whether striatal dopaminergic change in living RLS patients is net hypo-, hyper-, or simply dysregulated is unresolved by imaging (1999-turjanski-pet-dopamine-d2-binding.md vs 2012-kim-dat-spect-elderly-rls.md vs 2012-oboshi-pet-d2d3-treatment-response.md).
  • The D1-receptor-upregulation model of augmentation is untested in humans beyond a 10-subject non-powered pilot; a larger multicenter ecopipam trial is in development (2025-clemens-d1-d3-receptor-augmentation-model.md).
  • The relative weight of the dopamine-centric model versus the adenosine/"hypoadenosine" model as the true unifying mechanism is not settled (2026-baker-emerging-mechanisms-rls.md; 2025-mogavero-adenosine-hypothesis-critical-review.md).
  • Why some RLS patients have normal peripheral iron but low brain iron is unresolved; genetic variation in brain iron handling is one candidate but not proven causal in humans (2009-jellen-systems-genetics-brain-iron.md).
  • Long-term (multi-year), controlled data on de-prescribing dopamine agonists in already-augmented patients (versus preventing augmentation in treatment-naive patients) is sparse.

Notes in this topic

New notes written for this topic sweep:

  • 1999-turjanski-pet-dopamine-d2-binding.md — First PET evidence of reduced striatal D2 binding in RLS.
  • 2012-oboshi-pet-d2d3-treatment-response.md — Lower mesolimbic D2/3 PET binding predicts pramipexole response.
  • 2012-kim-dat-spect-elderly-rls.md — Increased striatal DAT density in elderly, drug-naive RLS patients.
  • 2010-barraud-a11-primate-neuroanatomy.md — A11 is the primate spinal cord's near-exclusive dopamine source, via D2/D3 receptors.
  • 2017-ozawa-a11-neuron-subtypes-spinal.md — A11 spinally-projecting neurons are molecularly heterogeneous (TH/calbindin subtypes).
  • 2007-zhao-a11-lesion-iron-deprivation-mice.md — Combined A11 lesion + iron deficiency synergistically alters D1/D2/D3 receptors and locomotion.
  • 2006-clemens-dopamine-hypothesis-spinal-cord.md — Hypothesis paper reframing RLS as a spinal dopaminergic (A11/D3) disorder.
  • 2004-clemens-d3-knockout-spinal-reflex.md — D3-receptor knockout reverses dopamine's normal inhibitory action on spinal reflexes.
  • 2005-clemens-tyrosine-hydroxylase-circadian-d3ko.md — D3 knockout inverts the circadian rhythm of spinal tyrosine hydroxylase.
  • 2011-dowling-d3-receptor-iron-deficient-mice.md — Iron deficiency and D3 knockout interact on sensory/circadian motor symptoms in mice.
  • 2012-deandrade-btbd9-mutant-mice.md — Btbd9 mutant mice show ropinirole-responsive RLS-like motor/sensory/iron phenotype.
  • 2016-allen-animal-models-rls-phenotypes.md — Review: BTBD9/MEIS1 genetics converge on iron regulation across species.
  • 2009-jellen-systems-genetics-brain-iron.md — QTL mapping links Btbd9, midbrain iron, and dopamine receptor expression in mice.
  • 2008-bianco-iron-deficiency-dat-levodopa.md — Iron deficiency reduces DAT and blunts/delays dopamine response to L-DOPA in rats.
  • 2010-quiroz-adenosine-a2a-iron-deficient-rats.md — Iron deficiency upregulates striatal adenosine A2A receptors in rats.
  • 2004-michaud-circadian-rhythm-melatonin.md — Rising evening melatonin precedes RLS symptom worsening.
  • 2005-michaud-circadian-immobility-symptoms.md — Immobility only worsens RLS discomfort during the ~21:20-08:00 window.
  • 2004-garcia-borreguero-neuroendocrine-ldopa-circadian.md — Nighttime-specific exaggerated neuroendocrine response to L-dopa in RLS.
  • 1999-montplaisir-pramipexole-crossover-rct.md — Early RCT: pramipexole normalizes PLMS index.
  • 2007-trenkwalder-cabergoline-levodopa-augmentation.md — RCT: cabergoline causes less augmentation than levodopa over 30 weeks.
  • 2023-zeng-augmentation-mechanisms-review.md — Review: augmentation rates by duration (10% short-term to 42-68% at ~10 years) and D1/D3 desensitization mechanism.
  • 2026-winkelman-rls-jama-clinical-review.md — 2026 JAMA review: gabapentinoids first-line, augmentation 7-10%/year, iron thresholds.
  • 2025-clemens-d1-d3-receptor-augmentation-model.md — Integrative D1/D3 receptor-balance model of RLS and augmentation, with ecopipam pilot data.

Pre-existing notes (found via duplicate check / cross-topic search, written by other topic sweeps):

  • 2009-connor-dopaminergic-profile-autopsy.md — Autopsy: decreased putamen D2R (correlated with severity), increased nigral/putamen TH.
  • 2007-ondo-animal-models-rls.md — Review of A11-lesion, iron-deprivation, and D3-knockout rodent models.
  • 2018-ferre-pivotal-adenosine-neurotransmission.md — Adenosine A1 downregulation model linking iron deficiency to presynaptic hyperdopaminergic and hyperglutamatergic states.
  • 2006-winkelman-pramipexole-fixed-dose-rct.md — 344-patient RCT establishing pramipexole efficacy across doses.
  • 2026-baker-emerging-mechanisms-rls.md — 2015-2025 decade review; dopamine/iron mechanisms hold, hypo-adenosine hypothesis emerging.
  • 2011-allen-community-survey-augmentation-incidence.md — Community survey: ~8%/year augmentation incidence, 20% prevalence.
  • 2011-hogl-pramipexole-6-month-augmentation-rct.md — RCT: pramipexole efficacy with 9.2% vs 6.0% augmentation at 6 months.
  • 2016-earley-connectome-dopamine-augmentation-mechanism.md — Review arguing RLS is not simply hypodopaminergic; PTPRD as candidate augmentation mediator.
  • 2014-earley-iron-dopamine-metabolic-theory-review.md — Review of CSF/autopsy/imaging evidence for iron-driven striatal dopamine dysfunction.
  • 2016-garcia-borreguero-augmentation-prevention-treatment-guidelines.md — IRLSSG/EURLSSG consensus on preventing/treating augmentation.
  • 2025-winkelman-aasm-guideline-rls.md — AASM 2024/2025 guideline: iron thresholds, gabapentinoids strong-recommended, dopamine agonists conditionally against.
  • 2022-earley-bid-rodent-model-review.md — Review validating brain-iron-deficiency rodent models against human RLS autopsy findings.
  • 2017-dinkins-d3-d1-receptor-animal-model.md — Chronic D3-agonist treatment induces a D1-reversible behavioral switch modeling augmentation.
  • 2007-qu-a11-lesion-iron-deprivation-mouse.md — Combined A11 lesion + iron deprivation model, reversed by ropinirole, worsened by D1 agonist.
  • 2016-quiroz-adenosine-a1-receptor-downregulation.md — Brain iron deficiency downregulates adenosine A1 receptors alongside D2 receptors.
  • 2025-mogavero-adenosine-hypothesis-critical-review.md — Critical review unifying dopamine, glutamate, and iron-deficiency threads via the adenosine hypothesis.
  • 2011-scholz-cochrane-levodopa-review.md — Cochrane review (9 RCTs, n=521): levodopa effective, but augmentation under-investigated.
  • 2013-garcia-borreguero-irlssg-long-term-guidelines.md — IRLSSG long-term efficacy grading: dopamine agonists Level A only to 6 months.
  • 2019-casoni-d3-receptor-agonist-efficacy-review.md — Pharmacology review: D3-preferring agonist action and a receptor-selectivity account of augmentation.
  • 2018-wang-acute-drug-withdrawal-rls-symptoms.md — PSG/EMG characterization of acute withdrawal from pramipexole, gabapentin, and oxycodone.
  • 2013-nirenberg-dopamine-agonist-withdrawal-review.md — Defines dopamine agonist withdrawal syndrome (DAWS); no proven effective treatment exists.

Additional linked notes (2026-09 quality pass)

These notes carry this topic tag but are not yet woven into the prose synthesis above; listed here so they are discoverable and counted in catalog.json rather than orphaned.

  • 2022-park-functional-connectivity-rls-review.md (2022) - Alterations of Functional Connectivity in Patients With Restless Legs Syndrome: This Korean-authored narrative review synthesizes functional-MRI connectivity studies in RLS, concluding that RLS patients show significant alterations relative to healthy controls in several brain networks - includin...

Geprüfte Studien zu diesem Thema (35)

Sortiert nach Evidenzgrad, dann nach Aktualität. Jeder Titel führt zum PubMed-Eintrag.

  • B

    Cabergoline compared to levodopa in the treatment of patients with severe restless legs syndrome: results from a multi-center, randomized, active controlled trial

    Trenkwalder C, Benes H, Grote L, Happe S, Hogl B, Mathis J, Saletu-Zyhlarz GM, Kohnen R · Movement Disorders · 2007

    RCTPMID 17274039

  • B

    Restless legs syndrome improved by pramipexole: a double-blind randomized trial

    Montplaisir J, Nicolas A, Denesle R, Gomez-Mancilla B · Neurology · 1999

    RCTPMID 10102409

  • C

    Increased striatal dopamine transporter density in moderately severe old restless legs syndrome patients

    Kim KW, Jhoo JH, Lee SB, Lee SD, Kim TH, Kim SE, Kim YK, Yoon IY · European Journal of Neurology · 2012

    Case ControlPMID 22435397

  • C

    In vivo mesolimbic D2/3 receptor binding predicts posttherapeutic clinical responses in restless legs syndrome: a positron emission tomography study

    Oboshi Y, Ouchi Y, Yagi S, Kono S, Nakai N, Yoshikawa E, Futatsubashi M, Terada T, Kim K, Harada K · Journal of Cerebral Blood Flow and Metabolism · 2012

    CohortPMID 22234337

  • C

    The dopamine transporter is decreased in the striatum of subjects with restless legs syndrome

    Earley CJ, Kuwabara H, Wong DF, Gamaldo C, Salas R, Brasic J, Ravert HT, Dannals RF, Allen RP · Sleep · 2011

    Case ControlPMID 21358851

  • C

    Elevated estradiol plasma levels in women with restless legs during pregnancy

    Dzaja A, Wehrle R, Lancel M, Pollmacher T · Sleep · 2009

    CohortPMID 19238803

  • C

    Circadian variation of the effects of immobility on symptoms of restless legs syndrome

    Michaud M, Dumont M, Paquet J, Desautels A, Fantini ML, Montplaisir J · Sleep · 2005

    Case ControlPMID 16124663

  • C

    Circadian variation in neuroendocrine response to L-dopa in patients with restless legs syndrome

    Garcia-Borreguero D, Larrosa O, Granizo JJ, de la Llave Y, Hening WA · Sleep · 2004

    RCTPMID 15283001

  • C

    Circadian rhythm of restless legs syndrome: relationship with biological markers

    Michaud M, Dumont M, Selmaoui B, Paquet J, Fantini ML, Montplaisir J · Annals of Neurology · 2004

    Case ControlPMID 14991815

  • C

    Striatal dopaminergic function in restless legs syndrome: 18F-dopa and 11C-raclopride PET studies

    Turjanski N, Lees AJ, Brooks DJ · Neurology · 1999

    Case ControlPMID 10102408

  • D

    Restless Legs Syndrome: A Review

    Winkelman JW, Wipper B · JAMA · 2026

    ReviewPMID 41563785

  • D

    Dopamine Receptors in Restless Legs Syndrome and Augmentation: A Novel Perspective Focused on D1 and D3 Receptor Dynamics

    Clemens S, Ondo WG, Paulus W · Movement Disorders · 2025

    ReviewPMID 40536089

  • D

    Exploring the causes of augmentation in restless legs syndrome

    Zeng P, Wang T, Zhang L, Guo F · Frontiers in Neurology · 2023

    ReviewPMID 37840917

  • D

    Alterations of Functional Connectivity in Patients With Restless Legs Syndrome

    Park KM, Kim KT, Kang KW, et al. · Journal of Clinical Neurology (Seoul, Korea) · 2022

    ReviewPMID 35589318

  • D

    Animal models of RLS phenotypes

    Allen RP, Donelson NC, Jones BC, Li Y, Manconi M, Rye DB, Sanyal S, Winkelmann J · Sleep Medicine · 2016

    ReviewPMID 27839945

  • D

    Restless legs syndrome: revisiting the dopamine hypothesis from the spinal cord perspective

    Clemens S, Rye D, Hochman S · Neurology · 2006

    ReviewPMID 16832090

  • E

    Comparative Peripheral Blood Transcriptomic Profiles in Parkinson's Disease and Restless Legs Syndrome: An Exploratory Between-Cohort Analysis

    Mogavero MP, Marchese G, Ventola GM, Lanza G, Clemens S, Salemi M, Bruni O, Ferri R · International Journal of Molecular Sciences · 2026

    CohortPMID 42589234

  • E

    BTBD9 and dopaminergic dysfunction in the pathogenesis of restless legs syndrome

    Lyu S, Doroodchi A, Xing H, Sheng Y, DeAndrade MP, Yang Y, Johnson TL, Clemens S, Yokoi F, Miller MA, Xiao R, Li Y · Brain Structure and Function · 2020

    AnimalPMID 32468214

  • E

    The role of BTBD9 in the cerebral cortex and the pathogenesis of restless legs syndrome

    Lyu S, Xing H, DeAndrade MP, Perez PD, Zhang K, Liu Y, Yokoi F, Febo M, Li Y · Experimental Neurology · 2019

    AnimalPMID 31715135

  • E

    The Role of BTBD9 in Striatum and Restless Legs Syndrome

    Lyu S, Xing H, DeAndrade MP, Liu Y, Perez PD, Yokoi F, Febo M, Walters AS, Li Y · eNeuro · 2019

    AnimalPMID 31444227

  • E

    Dopamine promotes cellular iron accumulation and oxidative stress responses in macrophages

    Dichtl S, Haschka D, Nairz M, Seifert M, Volani C, Lutz O, Weiss G · Biochemical Pharmacology · 2017

    In VitroPMID 29208364

  • E

    Three Types of A11 Neurons Project to the Rat Spinal Cord

    Ozawa H, Yamaguchi T, Hamaguchi S, Yamaguchi S, Ueda S · Neurochemical Research · 2017

    AnimalPMID 28303496

  • E

    Motor restlessness, sleep disturbances, thermal sensory alterations and elevated serum iron levels in Btbd9 mutant mice

    DeAndrade MP, Johnson RL, Unger EL, Zhang L, van Groen T, Gamble KL, Li Y · Human Molecular Genetics · 2012

    AnimalPMID 22678064

  • E

    Sleep fragmentation and motor restlessness in a Drosophila model of Restless Legs Syndrome

    Freeman A, Pranski E, Miller RD, Radmard S, Bernhard D, Jinnah HA, Betarbet R, Rye DB, Sanyal S · Current Biology · 2012

    AnimalPMID 22658601

  • E

    Dopamine D3 receptor specifically modulates motor and sensory symptoms in iron-deficient mice

    Dowling P, Klinker F, Stadelmann C, Hasan K, Paulus W, Liebetanz D · Journal of Neuroscience · 2011

    AnimalPMID 21209191

  • E

    Neuroanatomical study of the A11 diencephalospinal pathway in the non-human primate

    Barraud Q, Obeid I, Aubert I, Barriere G, Contamin H, McGuire S, Ravenscroft P, Porras G, Tison F, Bezard E, Ghorayeb I · PLoS ONE · 2010

    AnimalPMID 20967255

  • E

    The long-term effects of the dopamine agonist pramipexole in a proposed restless legs syndrome animal model

    Luo F, Li C, Ondo WG, Xu P, Xie W, Le W · Sleep Medicine · 2010

    AnimalPMID 21044864

  • E

    Up-regulation of striatal adenosine A(2A) receptors with iron deficiency in rats: effects on locomotion and cortico-striatal neurotransmission

    Quiroz C, Pearson V, Gulyani S, Allen R, Earley C, Ferre S · Experimental Neurology · 2010

    AnimalPMID 20385128

  • E

    Systems genetics analysis of iron regulation in the brain

    Jellen LC, Beard JL, Jones BC · Biochimie · 2009

    AnimalPMID 19393285

  • E

    Iron deficiency alters dopamine uptake and response to L-DOPA injection in Sprague-Dawley rats

    Bianco LE, Wiesinger J, Earley CJ, Jones BC, Beard JL · Journal of Neurochemistry · 2008

    AnimalPMID 18363828

  • E

    Lack of D2 receptor mediated regulation of dopamine synthesis in A11 diencephalospinal neurons in male and female mice

    Pappas SS, Behrouz B, Janis KL, Goudreau JL, Lookingland KJ · Brain Research · 2008

    AnimalPMID 18462709

  • E

    Spinal cord dopamine receptor expression and function in mice with 6-OHDA lesion of the A11 nucleus and dietary iron deprivation

    Zhao H, Zhu W, Pan T, Xie W, Zhang A, Ondo WG, Le W · Journal of Neuroscience Research · 2007

    AnimalPMID 17342757

  • E

    Reversal of the circadian expression of tyrosine-hydroxylase but not nitric oxide synthase levels in the spinal cord of dopamine D3 receptor knockout mice

    Clemens S, Sawchuk MA, Hochman S · Neuroscience · 2005

    AnimalPMID 15878801

  • E

    Conversion of the modulatory actions of dopamine on spinal reflexes from depression to facilitation in D3 receptor knock-out mice

    Clemens S, Hochman S · Journal of Neuroscience · 2004

    AnimalPMID 15601940

  • E

    Clinical correlates of 6-hydroxydopamine injections into A11 dopaminergic neurons in rats: a possible model for restless legs syndrome

    Ondo WG, He Y, Rajasekaran S, Le WD · Movement Disorders · 2000

    AnimalPMID 10634257

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