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  4. Translational research for improving the care of familial hypercholesterolemia: The “ten countries study” and beyond
 
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Translational research for improving the care of familial hypercholesterolemia: The “ten countries study” and beyond

Journal
Journal of Atherosclerosis and Thrombosis
Journal Volume
23
Journal Issue
8
Pages
891-900
Date Issued
2016
Author(s)
Watts G.F.
Ding P.Y.
George P.
Hagger M.S.
Hu M.
Lin J.
Khoo K.L.
Marais A.D.
Miida T.
Nawawi H.M.
Pang J.
Park J.E.
Gonzalez-Santos L.B.
TA-CHEN SU  
Truong T.H.
Santos R.D.
Soran H.
Yamashita S.
Tomlinson B.
Arikketh D.
Ashavaid T.F.
Atiqah N.
Balasubramaniam S.
Chan D.C.
NIEN-TZU CHANG  
Do T.C.
Zhao D.
Ellis K.L.
Han K.H.
Hardcastle S.J.
Jannes C.E.
Kassim A.M.
Ismail Z.M.
Kwok S.
Lam C.S.
Lansberg P.J.
Livingston M.
Mehta M.
Muir L.
Peng H.B.
Pereira A.C.
Rahman T.H.A.
Ramli A.S.
Rangarajan N.
Razak S.A.
Sijbrands E.J.
Sullivan D.R.
Shyong Tai E.
Tan H.C.
Verma I.C.
Wu X.
DOI
10.5551/jat.35949
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84980025252&doi=10.5551%2fjat.35949&partnerID=40&md5=ab9681cb2232f54269b84a5551a1a323
https://scholars.lib.ntu.edu.tw/handle/123456789/514773
Abstract
Familial hypercholesterolemia (FH) is the most common and serious form of inherited hyperlipidaemia. Dominantly inherited with high penetrance, untreated FH leads to premature death from coronary artery disease due to accelerated atherosclerosis from birth. Despite its importance, there is still a major shortfall in awareness, detection and treatment of FH worldwide. International models of care for FH have recently been published, but their effective implementation requires the garnering of more knowledge about the condition. The “Ten Countries Study” aims to investigate diagnostic, epidemiological and service aspects, as well as physician practices and patient experiences of FH in several countries in the Asia-Pacific Region and the Southern Hemisphere. Five observational studies are being undertaken that will systematically investigate the following aspects of FH: the phenotypic predictors of low-density lipoprotein receptor mutations, the point prevalence in available community populations, current knowledge and clinical practices among primary care physicians, availability and utilisation of services and facilities, and patient perceptions and personal experiences of the condition. The information gathered will inform better clinical practice and will enable the development of country-specific models of care for FH. ? 2016 Japan Atherosclerosis Society.
SDGs

[SDGs]SDG3

Other Subjects
apolipoprotein B; low density lipoprotein cholesterol; low density lipoprotein receptor; proprotein convertase 1; awareness; cardiovascular risk; familial hypercholesterolemia; gene mutation; genetic predisposition; genetic screening; genetic variability; health care; human; medication compliance; morbidity; outcome assessment; patient attitude; patient care; personal experience; phenotype; prevalence; primary health care; psychological aspect; questionnaire; Review; translational research; health care quality; Hyperlipoproteinemia Type II; standards; translational research; Humans; Hyperlipoproteinemia Type II; Quality of Health Care; Translational Medical Research
Publisher
Japan Atherosclerosis Society
Type
review

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