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Is there any link between vitamin D deficiency and vasovagal syncope?

BACKGROUND: This study aimed to investigate serum 25[OH]D levels between patients with vasovagal syncope (VVS) diagnosed with head‐up tilt table test (HUTT) and age‐matched healthy people. METHODS: The study included 75 consecutive patients (32.3 ± 10.7 years), who presented with syncope and underwe...

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Autores principales: Usalp, Songül, Kemal, Hatice, Yüksek, Ümit, Yaman, Belma, Günsel, Aziz, Edebal, Oğuzhan, Akpınar, Onur, Cerit, Levent, Duygu, Hamza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132194/
https://www.ncbi.nlm.nih.gov/pubmed/32256891
http://dx.doi.org/10.1002/joa3.12309
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author Usalp, Songül
Kemal, Hatice
Yüksek, Ümit
Yaman, Belma
Günsel, Aziz
Edebal, Oğuzhan
Akpınar, Onur
Cerit, Levent
Duygu, Hamza
author_facet Usalp, Songül
Kemal, Hatice
Yüksek, Ümit
Yaman, Belma
Günsel, Aziz
Edebal, Oğuzhan
Akpınar, Onur
Cerit, Levent
Duygu, Hamza
author_sort Usalp, Songül
collection PubMed
description BACKGROUND: This study aimed to investigate serum 25[OH]D levels between patients with vasovagal syncope (VVS) diagnosed with head‐up tilt table test (HUTT) and age‐matched healthy people. METHODS: The study included 75 consecutive patients (32.3 ± 10.7 years), who presented with syncope and underwent HUTT and 52 healthy controls (32.9 ± 14.1 years). HUTT patients were divided into two groups according to whether there was syncope response to the test. Patients underwent cardiac, psychiatric, and neurological investigation. Serum 25[OH]D levels were measured by chemiluminescent microparticle immunoassay method. RESULTS: There was no difference between the two groups in terms of age, gender, body mass index (BMI), echocardiographic findings (P > .05). Mean serum 25[OH]D (24.5 ± 6.3 vs 20.1 ± 8.8 ng/mL, P = .003) and vitamin B12 levels (436.4 ± 199.2 vs 363.1 ± 107.6 pg/mL, P = .009) was lower in syncope patients when compared to the control group. In correlation analyses, syncope was shown as correlated with the vitamin D (r = −264, P = .003) and vitamin B12 levels (r = −233, P = .009). But, multivariate regression analyses showed that only vitamin D increased risk of syncope [OR: 0.946, 95% CI (0.901‐0.994)]. There was no difference in terms of age, gender, BMI, echocardiographic findings between the in HUTT positive (n = 45) and negative groups (n = 29). Only vitamin D level was significantly lower in HUTT positive group (17.5 ± 7.7 vs 24.4 ± 9.1 ng/mL, P = .002). There was no difference among in the vasovagal subgroups in terms of vitamin D level and other features. CONCLUSION: Vitamin D and B12 levels were reasonably low in syncope patients, but especially low Vitamin D levels were associated with VVS diagnosed in HUTT.
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spelling pubmed-71321942020-04-06 Is there any link between vitamin D deficiency and vasovagal syncope? Usalp, Songül Kemal, Hatice Yüksek, Ümit Yaman, Belma Günsel, Aziz Edebal, Oğuzhan Akpınar, Onur Cerit, Levent Duygu, Hamza J Arrhythm Original Article BACKGROUND: This study aimed to investigate serum 25[OH]D levels between patients with vasovagal syncope (VVS) diagnosed with head‐up tilt table test (HUTT) and age‐matched healthy people. METHODS: The study included 75 consecutive patients (32.3 ± 10.7 years), who presented with syncope and underwent HUTT and 52 healthy controls (32.9 ± 14.1 years). HUTT patients were divided into two groups according to whether there was syncope response to the test. Patients underwent cardiac, psychiatric, and neurological investigation. Serum 25[OH]D levels were measured by chemiluminescent microparticle immunoassay method. RESULTS: There was no difference between the two groups in terms of age, gender, body mass index (BMI), echocardiographic findings (P > .05). Mean serum 25[OH]D (24.5 ± 6.3 vs 20.1 ± 8.8 ng/mL, P = .003) and vitamin B12 levels (436.4 ± 199.2 vs 363.1 ± 107.6 pg/mL, P = .009) was lower in syncope patients when compared to the control group. In correlation analyses, syncope was shown as correlated with the vitamin D (r = −264, P = .003) and vitamin B12 levels (r = −233, P = .009). But, multivariate regression analyses showed that only vitamin D increased risk of syncope [OR: 0.946, 95% CI (0.901‐0.994)]. There was no difference in terms of age, gender, BMI, echocardiographic findings between the in HUTT positive (n = 45) and negative groups (n = 29). Only vitamin D level was significantly lower in HUTT positive group (17.5 ± 7.7 vs 24.4 ± 9.1 ng/mL, P = .002). There was no difference among in the vasovagal subgroups in terms of vitamin D level and other features. CONCLUSION: Vitamin D and B12 levels were reasonably low in syncope patients, but especially low Vitamin D levels were associated with VVS diagnosed in HUTT. John Wiley and Sons Inc. 2020-02-10 /pmc/articles/PMC7132194/ /pubmed/32256891 http://dx.doi.org/10.1002/joa3.12309 Text en © 2020 The Authors. Journal of Arrhythmia published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Heart Rhythm Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Usalp, Songül
Kemal, Hatice
Yüksek, Ümit
Yaman, Belma
Günsel, Aziz
Edebal, Oğuzhan
Akpınar, Onur
Cerit, Levent
Duygu, Hamza
Is there any link between vitamin D deficiency and vasovagal syncope?
title Is there any link between vitamin D deficiency and vasovagal syncope?
title_full Is there any link between vitamin D deficiency and vasovagal syncope?
title_fullStr Is there any link between vitamin D deficiency and vasovagal syncope?
title_full_unstemmed Is there any link between vitamin D deficiency and vasovagal syncope?
title_short Is there any link between vitamin D deficiency and vasovagal syncope?
title_sort is there any link between vitamin d deficiency and vasovagal syncope?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132194/
https://www.ncbi.nlm.nih.gov/pubmed/32256891
http://dx.doi.org/10.1002/joa3.12309
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