Current Vascular Pharmacology

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The Gulf Familial Hypercholesterolemia Registry (Gulf FH): Design, Rationale and Preliminary Results
Current Vascular Pharmacology - Tập 18 Số 1 - Trang 57-64 - 2019
Khalid Al‐Rasadi, Khalid F. AlHabib, Faisal A. Al-Allaf, Khalid Al-Waili, Ibrahim Al‐Zakwani, Ahmad Al‐Sarraf, Wael Almahmeed, Nasreen Al-Sayed, Mohammad Alghamdi, Mohammed A. Batais, Turky H. Almigbal, Fahad Alnouri, Abdulhalim Jamal Kinsara, Ashraf Hammouda, Zuhier Awan, Heba Kary, Omer A. Elamin, Fahad Zadjali, Mohammed Al‐Jarallah, Abdullah Shehab, Hani Sabbour, Haitham Amin, Hani Altaradi
Aim:

To determine the prevalence, genetic characteristics, current management and outcomes of familial hypercholesterolaemia (FH) in the Gulf region.

Methods:

Adult (18-70 years) FH patients were recruited from 9 hospitals and centres across 5 Arabian Gulf countries. The study was divided into 4 phases and included patients from 3 different categories. In phase 1, suspected FH patients (category 1) were collected according to the lipid profile and clinical data obtained through hospital record systems. In phase 2, patients from category 2 (patients with a previous clinical diagnosis of FH) and category 1 were stratified into definitive, probable and possible FH according to the Dutch Lipid Clinic Network criteria. In phase 3, 500 patients with definitive and probable FH from categories 1 and 2 will undergo genetic testing for 4 common FH genes. In phase 4, these 500 patients with another 100 patients from category 3 (patients with previous genetic diagnosis of FH) will be followed for 1 year to evaluate clinical management and cardiovascular outcomes. The Gulf FH cohort was screened from a total of 34,366 patients attending out-patient clinics.

Results:

The final Gulf FH cohort consisted of 3,317 patients (mean age: 47±12 years, 54% females). The number of patients with definitive FH is 203. In this initial phase of the study, the prevalence of (probable and definite) FH is 1/232.

Conclusion:

The prevalence of FH in the adult population of the Arabian Gulf region is high. The Gulf FH registry, a first-of-a-kind multi-national study in the Middle East region, will help in improving underdiagnosis and undertreatment of FH in the region.

Prevalence, Diagnosis, and Treatment with 3 Different Statins of Non-alcoholic Fatty Liver Disease/Non-alcoholic Steatohepatitis in Military Personnel. Do Genetics Play a Role?
Current Vascular Pharmacology - Tập 19 Số 5 - Trang 572-581 - 2021
Georgios Sfikas, Michael Psallas, Charalambos Koumaras, Κonstantinos Imprialos, Evangelos Perdikakis, Michael Doumas, Όλγα Γιουλεμέ, Asterios Karagiannis, Vasilios G. Athyros
Background:

Non-alcoholic fatty liver disease (NAFLD) and its severe form, non-alcoholic steatohepatitis (NASH), are major health problems worldwide. Genetics may play a role in the pathogenesis of NAFLD/NASH.

Aim:

To investigate the prevalence of NAFLD/NASH in 5,400 military personnel and evaluate the effect of treatment with 3 statins on NAFLD/NASH using 2 non-invasive scores [NAFLD Activity Score (NAS); Fibrosis-4 score (FIB-4)].

Methods:

During the mandatory annual medical check-up, military personnel underwent a clinical and laboratory evaluation. Participants with NAFLD/NASH were randomized into 4 groups (n=151 each): diet-exercise, atorvastatin, rosuvastatin, or pitavastatin for 1 year (i.e., until the next routine evaluation).

Results:

From all the participants, 613 had NAFLD/NASH (prevalence 11.3 vs 39.8% in the general population, p<0.001), and a total of 604 consented to participate in the study. After a year of treatment, the diet-exercise group showed no significant changes in both scores (NAS 4.98 baseline vs. 5.62, p=0.07; FIB-4 3.42 vs. 3.52, p=0.7). For the atorvastatin group, both scores were reduced (NAS 4.97 vs 1.95, p<0.001, FIB-4 3.56 vs 0.83, p<0.001), for rosuvastatin (NAS 5.55 vs 1.81, p<0.001, FIB-4 3.61 vs 0.79, p<0.001), and for pitavastatin (NAS 4.89 vs 1.99, p<0.001, FIB-4 3.78 vs 0.87, p<0.001).

Conclusions :

Atorvastatin, rosuvastatin, and pitavastatin have a beneficial and safe effect in NAFLD/NASH patients as recorded by the improvement in the NAS (representing NAFLD activity) and FIB-4 (representing liver fibrosis) scores. Since both those with and without NAFLD/- NASH shared several baseline characteristics, genetics may play a role in the pathogenesis of NAFLD/NASH and its treatment with statins.

Assessing The Treatment Effect in Metabolic Syndrome Without Perceptible Diabetes (ATTEMPT): A Prospective-Randomized Study in Middle Aged Men and Women
Current Vascular Pharmacology - Tập 9 Số 6 - Trang 647-657 - 2011
Vasilios G. Athyros, Emmanuel S. Ganotakis, Genovefa Kolovou, Vassilios Nicolaou, Apostolos Achimastos, E. Bilianou, Theodore K. Alexandrides, Asterios Karagiannis, Konstantinos Paletas, Evangelos Liberopoulos, Κωνσταντίνος Τζιόμαλος, Dimitris Petridis, Anna I. Kakafika, Moses Elisaf, Dimitri P. Mikhailidis
miR-135a Suppresses Calcification in Senescent VSMCs by Regulating KLF4/STAT3 Pathway
Current Vascular Pharmacology - Tập 14 Số 2 - Trang 211-218 - 2016
Lin Lin, Yue He, Beili Xi, Hongchao Zheng, Qian Chen, ­Jun Li­, Ying Hu, Ming-Hao Ye, Ping Chen, Yi Qu
Pharmacological Therapy of Abdominal Aortic Aneurysm: An Update
Current Vascular Pharmacology - Tập 16 Số 2 - Trang 114-124 - 2018
Yidong Wang, Zhenjie Liu, Jun Ren, Meixiang Xiang
How to Identify Subjects with Poly-Vascular Disease?
Current Vascular Pharmacology - Tập 10 Số 6 - Trang 728-730 - 2012
Charalambos Vlachopoulos, Dimitrios Terentes‐Printzios, Christodoulos Stefanadis
The Role of microRNA-126 in Vascular Homeostasis
Current Vascular Pharmacology - Tập 13 Số 3 - Trang 341-351 - 2015
Coen van Solingen, Roel Bijkerk, Hetty C. de Boer, Ton J. Rabelink, Anton Jan van Zonneveld
Glucocorticoids and Vascular Reactivity
Current Vascular Pharmacology - Tập 2 Số 1 - Trang 1-12 - 2004
Shumei Yang, Li Zhang
Animal Models for Studying Neointima Formation
Current Vascular Pharmacology - Tập 8 Số 2 - Trang 198-219 - 2010
Jamie Y. Jeremy, Anita C Thomas
Involvement of Coagulation and Hemostasis in Inflammatory Bowel Diseases
Current Vascular Pharmacology - Tập 10 Số 5 - Trang 659-669 - 2012
Antoni Stadnicki
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