Dopamine beta hydroxylase deficiency
| Dopamine beta hydroxylase deficiency | |
|---|---|
| Other names | DβH deficiency |
 | |
| Dopamine beta hydroxylase is the enzyme responsible for converting dopamine (pictured) to norepinephrine. | |
Dopamine beta (β)-hydroxylase deficiency is a human medical condition involving inadequate dopamine beta-hydroxylase. It is characterized by increased amounts of serum dopamine and the absence of norepinephrine (NE) and epinephrine.
Dopamine is released, as a false neurotransmitter, in place of norepinephrine (aka noradrenaline and noradrenalin). This condition is sometimes referred to as "norepinephrine deficiency". Researchers of disorders such as schizophrenia are interested in studying this disorder, as patients with these specific diseases can have an increase in the amount of dopamine in their system and yet do not show other symptoms of DβH deficiency.
Dopamine beta-hydroxylase deficiency is a rare form of dysautonomia. It belongs to the class of rare diseases, with "a prevalence of fewer than 20 affected individuals, all of Western European descent". It is an autosomal recessive disorder caused by a mutation in the DβH gene, which results in the production of a nonfunctional dopamine β-hydroxylase enzyme.[1] Without this enzyme, patients with DβH deficiency develop many clinical manifestations that affect their daily lives.
Signs and symptoms
[edit]Dopamine beta (β)-hydroxylase deficiency affects the autonomic nervous system (ANS). The ANS works via two opposing branches, the sympathetic and parasympathetic, both of which antagonistically control involuntary processes that regulate body homeostasis. Problems related to DβH deficiency often appear as complications shortly after birth. Postnatal symptoms may include vomiting, dehydration, hypotension, muscle hypotonia, hypothermia, and hypoglycemia.[2]
Due to the deficiency of norepinephrine and epinephrine, those affected may present with droopy eyelids (ptosis), nasal congestion, and hypotension. The most common complaint is orthostatic hypotension. The symptoms associated with orthostatic hypotension are dizziness, blurred vision, and fainting upon standing. Patients may have difficulty with prolonged standing. This phenomenon is especially pronounced when going from horizontal to upright, such as getting out of bed. It is worsened by hot climates due to loss of fluid through sweating. Difficulty maintaining normal blood pressure makes it difficult to exercise (exercise intolerance). Males may experience retrograde ejaculation, a discharge of semen backward into the bladder due to dysmotility of their smooth muscle, which is innervated by the ANS. A subset of patients present with hypermobility.[1] Postural orthostatic tachycardia syndrome, another form of dysautonomia, also displays this comorbidity with hypermobility in the form of a rare connective tissue disorder called Ehlers Danlos syndrome.[citation needed]
Another commonly experienced symptom is hypoglycemia, which is thought to be caused by adrenomedullary failure. Loss of noradrenergic control is seen as T-wave abnormalities on electrocardiogram. Prolactin is frequently suppressed by excessive dopamine found in the central nervous system. Excess dopamine can also affect digestion, producing vomiting and inhibiting motor signaling to the GI tract.[3]
Cause
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Diagnosis
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Treatment
[edit]Lifestyle
[edit]Untreated individuals should avoid hot environments, strenuous exercise, prolonged standing and dehydration. Care should be taken when moving from horizontal to upright.[3]
Medications
[edit]L-threo-DOPS is a synthetic precursor of noradrenaline. The conversion of dihydroxyphenylserine (Droxidopa; trade name: Northera; also known as L-DOPS, L-threo-dihydroxyphenylserine, L-threo-DOPS and SM-5688), to norepinephrine bypasses the dopamine beta-hydroxylation step of catecholamine synthesis, L-Threo-DOPS is the preferred therapeutic agent.[4][5][6][7] In humans, L-Threo-DOPS administration has proven effective in managing blood pressure and postural symptoms.[8]
L-DOPS continues to be studied pharmacologically and pharmacokinetically and shows an ability to significantly increase the levels of central nervous system norepinephrine, even though L-DOPS has a relative difficulty crossing the blood-brain barrier when compared to medications such as L-DOPA. Concurrent use increases efficacy, as they are both involved and connected to the norepinephrine synthesis pathway.[citation needed]
L-DOPS may eventually to help other conditions or symptoms such as pain, chronic stroke symptoms, and progressive supranuclear palsy. Clinically, L-DOPS has been reported to be helpful in treating other conditions related to hypotension such as:[citation needed]
- Diabetes induced orthostatic hypotension
- Dialysis-induced hypotension
- Orthostatic intolerance
- Familial amyloidotic polyneuropathy
- Spinal Cord Injury related hypotension[9]
Empirical evidence of mild effectiveness has been reported using mineralocorticoids or adrenergic receptor agonists as therapies.[2]
Other medications that can bring relief to symptoms include:[10]
- phenylpropanolamine- due to pressor response to vascular α-adrenoceptors
- indomethacin
Vitamin C (ascorbic acid) is a required cofactor for the Dopamine beta hydroxylase enzyme. Vitamin C rapidly catalyzes the conversion of dopamine to norepinephrine through stimulation of dopamine beta hydroxylase.[10]
Prognosis
[edit]This is a form of dysautonomia distinct from familial dysautonomia because of its lack of familial dysautonomic symptoms such as loss of sense of pain and smell. L-threo-DOPS has been described as being "very effective for restoring noradrenergic tone and correcting postural hypotension, response to treatment is variable and the long-term and functional outcome is unknown."[11]
Research
[edit]Researchers have gathered retrospective data collections in order to better under the progression of this orphan disease. Most studies show a perinatal period marked by inadequacy of the ANS to control blood pressure, blood sugar, and body temperature. The experiences of orthostatic hypotension, exercise intolerance, and "traumatic morbidity related to falls and syncope" have been documented later in lives of people with this condition.[2] To provide a basis for improving the epidemiology, genotype/phenotype correlation, outcome of these diseases, their impact on the quality of life of patients, and for evaluating diagnostic and therapeutic strategies, a patient registry was established by the non-commercial International Working Group on Neurotransmitter Related Disorders (iNTD).[12]
Studies have explored the connection between DβH deficiency, Droxidopa treatment, and the effect on orthostatic tolerance and glucose homeostasis. It was reported that Droxidopa increased acute and late glucose-stimulated insulin secretion and improved patients' insulin sensitivity. However, the use of Droxidopa was found to produce only "modest changes in glucose homeostasis". This shows that treatment modalities other than Droxidopa should be pursued as possible adjuncts for the hyperinsulinemia seen in DβH deficiency.[13]
References
[edit]- ^ a b Reference, Genetics Home. "dopamine beta-hydroxylase deficiency". Genetics Home Reference. Retrieved 2016-12-15.
- ^ a b c Senard, Jean-Michel; Rouet, Philippe (2006-01-01). "Dopamine beta-hydroxylase deficiency". Orphanet Journal of Rare Diseases. 1: 7. doi:10.1186/1750-1172-1-7. ISSN 1750-1172. PMC 1459119. PMID 16722595.
- ^ a b "Dopamine receptor antagonists - Pharmacorama". www.pharmacorama.com. Archived from the original on 2016-12-13. Retrieved 2016-12-15.
- ^ Kaufmann, Horacio; Saadia, Daniela; Voustianiouk, Andrei; Goldstein, David S.; Holmes, Courtney; Yahr, Melvin D.; Nardin, Rachel; Freeman, Roy (2003-08-12). "Norepinephrine Precursor Therapy in Neurogenic Orthostatic Hypotension". Circulation. 108 (6): 724–728. doi:10.1161/01.CIR.0000083721.49847.D7. ISSN 0009-7322. PMID 12885750.
- ^ Mathias, C. J.; Senard, J. M.; Braune, S.; Watson, L.; Aragishi, A.; Keeling, J. E.; Taylor, M. D. (2001-08-01). "L-threo-dihydroxyphenylserine (L-threo-DOPS; droxidopa) in the management of neurogenic orthostatic hypotension: a multi-national, multi-center, dose-ranging study in multiple system atrophy and pure autonomic failure". Clinical Autonomic Research. 11 (4): 235–242. doi:10.1007/bf02298955. ISSN 0959-9851. PMID 11710796. S2CID 24567321.
- ^ Isaacson, Stuart; Skettini, Julia (2014-04-03). "Neurogenic orthostatic hypotension in Parkinson's disease: evaluation, management, and emerging role of droxidopa". Vascular Health and Risk Management. 10: 169–76. doi:10.2147/vhrm.s53983. PMC 3979788. PMID 24729712.
- ^ Biaggioni, Italo; Freeman, Roy; Mathias, Christopher J.; Low, Phillip; Hewitt, L. Arthur; Kaufmann, Horacio (2015-01-01). "Randomized Withdrawal Study of Patients With Symptomatic Neurogenic Orthostatic Hypotension Responsive to DroxidopaNovelty and Significance". Hypertension. 65 (1): 101–107. doi:10.1161/HYPERTENSIONAHA.114.04035. ISSN 0194-911X. PMC 4354798. PMID 25350981.
- ^ Biaggioni, Italo; Robertson, David (1987). "Endogenous Restoration of Noradrenaline by Precursor Therapy in Dopamine-Beta-Hydroxylase Deficiency". The Lancet. 330 (8569): 1170–1172. doi:10.1016/s0140-6736(87)91317-1. PMID 2890806. S2CID 43845850.
- ^ Goldstein, David S. (2006-09-01). "L-Dihydroxyphenylserine (L-DOPS): A Norepinephrine Prodrug". Cardiovascular Drug Reviews. 24 (3–4): 189–203. doi:10.1111/j.1527-3466.2006.00189.x. ISSN 1527-3466. PMID 17214596.
- ^ a b Robertson, David; Garland, Emily M. (1993-01-01). "Dopamine Beta-Hydroxylase Deficiency". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora J.H.; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). GeneReviews. Seattle (WA): University of Washington, Seattle. PMID 20301647.
- ^ Robertson, David; Goldberg, Michael R.; Onrot, Jack; Hollister, Alan S.; Wiley, Ron; Thompson, John G. Jr.; Robertson, Rose Marie (1986-06-05). "Isolated Failure of Autonomic Noradrenergic Neurotransmission". New England Journal of Medicine. 314 (23): 1494–1497. doi:10.1056/NEJM198606053142307. ISSN 0028-4793. PMID 3010116.
- ^ "Patient Registry".
- ^ Arnold, Amy C.; Garland, Emily M.; Celedonio, Jorge E.; Raj, Satish R.; Abumrad, Naji N.; Biaggioni, Italo; Robertson, David; Luther, James M.; Shibao, Cyndya A. (2016-10-25). "Hyperinsulinemia and Insulin Resistance in Dopamine β-Hydroxylase Deficiency". The Journal of Clinical Endocrinology & Metabolism. 102 (1): jc.2016–3274. doi:10.1210/jc.2016-3274. ISSN 0021-972X. PMC 5413093. PMID 27778639.
Further reading
[edit]- GeneReviews/NCBI/NIH/UW entry on Dopamine Beta-Hydroxylase Deficiency
- Fu W, Shen J, Luo X, et al. (September 2007). "Dopamine D1 receptor agonist and D2 receptor antagonist effects of the natural product (-)-stepholidine: molecular modeling and dynamics simulations". Biophysical Journal. 93 (5): 1431–41. Bibcode:2007BpJ....93.1431F. doi:10.1529/biophysj.106.088500. PMC 1948031. PMID 17468175.
- Alaniz RC, Thomas SA, Perez-Melgosa M, et al. (March 1999). "Dopamine beta-hydroxylase deficiency impairs cellular immunity". Proceedings of the National Academy of Sciences of the United States of America. 96 (5): 2274–8. Bibcode:1999PNAS...96.2274A. doi:10.1073/pnas.96.5.2274. PMC 26773. PMID 10051631.