Literature DB >> 23978222

A double-blind placebo-controlled cross-over study of the vascular effects of midodrine in neuropathic compared with hyperadrenergic postural tachycardia syndrome.

Amanda J Ross1, Anthony J Ocon, Marvin S Medow, Julian M Stewart.   

Abstract

POTS (postural tachycardia syndrome) is a chronic form of OI (orthostatic intolerance). Neuropathic POTS is characterized by decreased adrenergic vasoconstriction, whereas hyperadrenergic POTS exhibits increased adrenergic vasoconstriction. We hypothesized that midodrine, an α1-adrenergic receptor agonist, would increase CVR (calf vascular resistance), decrease C(v) (calf venous capacitance) and decrease orthostatic tachycardia in neuropathic POTS, but not alter haemodynamics in hyperadrenergic POTS. A total of 20 POTS patients (12 neuropathic and eight hyperadrenergic), ages 12-20 years, participated in this randomized placebo-controlled double-blind cross-over study. Of these subjects, 15 were female. POTS subjects received 2 weeks of treatment with midodrine or placebo, with increased dosing from 2.5 to 10 mg three times daily. Following a 7-day drug-washout period, subjects received the cross-over treatment. HR (heart rate), MAP (mean arterial pressure), Q(calf) (calf blood flow) and CVR were measured supine and during 35° HUT (head-up tilt). C(v) was measured supine. In neuropathic POTS, midodrine decreased supine HR, Q(calf) and C(v), while increasing MAP and CVR compared with placebo. During HUT, in neuropathic POTS, midodrine decreased HR, Q(calf) and C(v), while increasing MAP and CVR. In hyperadrenergic POTS, placebo and midodrine both decreased upright HR and increased supine CVR. Placebo also increased supine C(v), compared with midodrine in hyperadrenergic POTS. Therefore midodrine improved postural tachycardia in neuropathic POTS by increasing CVR and decreasing Q(calf) and C(v), whereas these effects were not seen in hyperadrenergic POTS patients who experienced a placebo effect. This suggests that midodrine is probably an effective treatment for neuropathic POTS, but not for hyperadrenergic POTS.

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Year:  2014        PMID: 23978222      PMCID: PMC3896075          DOI: 10.1042/CS20130222

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  22 in total

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2.  The placebo effect. A neglected asset in the care of patients.

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5.  Hemodynamic and symptomatic effects of acute interventions on tilt in patients with postural tachycardia syndrome.

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  17 in total

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Review 3.  Pediatric Disorders of Orthostatic Intolerance.

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5.  Blunted cerebral blood flow velocity in response to a nitric oxide donor in postural tachycardia syndrome.

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6.  Impaired Endothelial Function in Patients With Postural Tachycardia Syndrome.

Authors:  Abby H Chopoorian; Amr Wahba; Jorge Celedonio; Victor Nwazue; Emily C Smith; Emily M Garland; Sachin Paranjape; Luis E Okamoto; Bonnie K Black; Italo Biaggioni; Satish R Raj; Alfredo Gamboa
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Review 7.  Neuronal and hormonal perturbations in postural tachycardia syndrome.

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8.  Decreasing cerebral oxygen consumption during upright tilt in vasovagal syncope.

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