Long-term clinical use of mirabegron in patients with overactive bladder syndrome

2020 ◽  
Vol 13 (4) ◽  
pp. 460-464
Author(s):  
Tomasz Wiatr ◽  
Piotr Chłosta

Overactive bladder syndrome (OAB) is defined by the International Continence Society (ICS) as urinary urgency with increased daytime frequency and nocturia in the absence of proven infection or any other pathology, usually with or without urgency incontinence. Pharmacotherapy with antimuscarinic drugs is highly effective, but more than 60% of patients discontinue the treatment. Development of mirabegron, a β3-adrenoceptor agonist (β3-AR), has become an expected pharmacotherapy option for the non-invasive treatment of overactive bladder. The available studies show that long-term treatment with 50 mg mirabegron in patients with OAB is associated with reducing the severity of symptoms. Data from clinical trials show that mirabegron provides efficacy similar to antimuscarinic drugs, but with a better tolerance profile.

2018 ◽  
Vol 6 (1) ◽  
pp. 1
Author(s):  
Yoshihito Murakami ◽  
Hiroshi Nagae ◽  
Naomi Maehori ◽  
Hidehisa Sekijima ◽  
Kazuya Ooi

1989 ◽  
Vol 12 (10) ◽  
pp. 664-667 ◽  
Author(s):  
C. Mousson ◽  
S.A. Charhon ◽  
M. Ammar ◽  
M. Accominotti ◽  
G. Rifle

The accumulation of aluminium (AI) can cause AI bone deposits, osteomalacia and encephalopathy. As albumin solutions used as replacement fluid in plasma exchange (PE) are contaminated with AI, we studied AI overload in two symptomless patients with normal renal function, treated by long-term plasma exchange (PE). Total AI loading was calculated at 1750 μmol in patient 1 (178 PE sessions) and 2100 μmol in patient 2 (153 PE sessions). Bone biopsy showed AI deposits and low bone formation without osteomalacia in patient 1 and only osteoporosis in patient 2. Plasma AI levels were useless in detecting early AI overload, because the remained in the normal range, even after PE in both patients. Bone biopsy was the best means of recognizing AI intoxication, but cannot be recommended for frequent evaluations. However, the desferrioxamine mobilization test can be proposed as a repetitive non-invasive investigation method.


2019 ◽  
Author(s):  
Karin Rustler ◽  
Galyna Maleeva ◽  
Alexandre M. J. Gomila ◽  
Pau Gorostiza ◽  
Piotr Bregestovski ◽  
...  

The <i>γ</i>-aminobutyric acid gated chloride channel represents the major mediator of inhibitory neurotransmission in the mammalian central nervous system and its dysfunction is related to severe diseases like epilepsy and depression, which can be relieved by the application of allosteric modulators. However, the drugs’ potential side-effects limit their application for long-term treatment. Applying light as external stimulus to modify the pharmacophore’s activity, as emerged in the field of photopharmacology, provides a non-invasive tool with high spatial and temporal resolution for the modulation of protein function. Herein, we report the design, synthesis, and biological evaluation of photochromic fulgimide-based benzodiazepine derivatives as light-controllable potentiators of GABA<sub>A</sub> receptors (GABA<sub>A</sub>Rs). A photocontrolled potentiator of GABA<sub>A</sub>Rs (Fulgazepam) has been identified that does not display agonist or antagonist activity and allows manipulating zebrafish larvae swimming.


2019 ◽  
Vol 38 (2) ◽  
pp. 779-792 ◽  
Author(s):  
Elizabeth R. Mueller ◽  
Rob van Maanen ◽  
Christopher Chapple ◽  
Paul Abrams ◽  
Sender Herschorn ◽  
...  

2013 ◽  
Vol 189 (6) ◽  
pp. 2194-2201 ◽  
Author(s):  
Kenneth M. Peters ◽  
Donna J. Carrico ◽  
Leslie S. Wooldridge ◽  
Christopher J. Miller ◽  
Scott A. MacDiarmid

2016 ◽  
Vol 36 (6) ◽  
pp. 1511-1518 ◽  
Author(s):  
Fabiano B. Calmasini ◽  
Mariana G. de Oliveira ◽  
Eduardo C. Alexandre ◽  
Fábio H. da Silva ◽  
Carmem P.V. da Silva ◽  
...  

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