2019
DOI: 10.1016/j.anai.2018.10.004
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Flow-mediated vasodilation assay indicates no endothelial dysfunction in hereditary angioedema patients with C1-inhibitor deficiency

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Cited by 4 publications
(3 citation statements)
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“…A similar study by Birjmohun et al, which evaluated the effects of short-and long-term danazol treatment, revealed decreased apoA-I and HDL-cholesterol levels in short-term treated patients in comparison to the baseline measures, while long-term treatment did not adversely affect HDL-cholesterol concentration and apolipoproteins between patients and controls [36]. A more recent study by Nebenführer et al revealed that danazol treated patients suffering from hereditary angioedema with C1 inhibitor deficiency had higher cardiovascular risk, as evaluated by the high body mass index and LDL/HDL ratio, in comparison to healthy controls [238].…”
Section: Hdl In Angioedemamentioning
confidence: 95%
“…A similar study by Birjmohun et al, which evaluated the effects of short-and long-term danazol treatment, revealed decreased apoA-I and HDL-cholesterol levels in short-term treated patients in comparison to the baseline measures, while long-term treatment did not adversely affect HDL-cholesterol concentration and apolipoproteins between patients and controls [36]. A more recent study by Nebenführer et al revealed that danazol treated patients suffering from hereditary angioedema with C1 inhibitor deficiency had higher cardiovascular risk, as evaluated by the high body mass index and LDL/HDL ratio, in comparison to healthy controls [238].…”
Section: Hdl In Angioedemamentioning
confidence: 95%
“…However, the topic is still controversial and Nebenfuhrer et al in a very recent study report no signs of endothelial dysfunction in HAE patients [91]. They performed ultrasound assessment of endothelium-dependent flow-mediated dilation of the brachial artery in 33 C1-INH-HAE patients and in 30 healthy matched controls.…”
Section: Measurement Of Impaired Endothelial Functionmentioning
confidence: 99%
“…Hereditary angioedema is a rare genetic disorder that is caused by a deficiency or dysfunction of C1 esterase inhibitor (C1 INH), which leads to recurrent episodes of bradykinin‐mediated edema 1 . Triggers for attacks vary by patient, and the consequences can range from pain in the swollen area to life‐threatening airway restriction 2 .…”
Section: Introductionmentioning
confidence: 99%