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Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents
Purpose of Review To elucidate the current approach of care in pediatric patients with familial hypercholesterolemia (FH). We sought an answer to the question whether the advances and major changes in lipid management are relevant and apply to children and adolescents. Recent Findings Latest researc...
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Published in: | Current atherosclerosis reports 2021-06, Vol.23 (6), p.30-30, Article 30 |
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creator | Cohen, Hofit Stefanutti, Claudia |
description | Purpose of Review
To elucidate the current approach of care in pediatric patients with familial hypercholesterolemia (FH). We sought an answer to the question whether the advances and major changes in lipid management are relevant and apply to children and adolescents.
Recent Findings
Latest research findings clearly demonstrate that lowering cholesterol levels at a young age prevents vascular atherosclerotic changes and decreases cardiovascular events in adulthood and emphasizes the importance of early detection and intervention in the pediatric FH patients group.
Summary
FH is a common genetic disease caused by mutations in genes associated with the metabolism of low-density lipoproteins (LDL). The hallmark of FH is elevated LDL cholesterol (LDL-C) levels from birth and premature atherosclerotic cardiovascular disease (ASCVD). Often FH is either undiagnosed or diagnosed with a considerable delay, leading to vascular atherosclerotic changes and cardiovascular disease. Prompt identification of FH subjects is essential, to initiate early preventive measures. Safe and efficient pharmacological agents are approved for use in children and adolescents. Statins are the first line of therapy, in combination of ezetimibe. Unfortunately, these drugs do not warrant the achievement of therapeutic target, especially in HoFH patient. In the latter, lipoprotein apheresis (LA), which has been shown to be safe and effective, is strongly recommended. Finally, the new drugs still under study will allow a multimodal customized treatment. Lowering cholesterol levels at a young age hinders vascular atherosclerotic changes decreasing cardiovascular events in adulthood. Therefore, early detection, diagnosis, and intervention in FH patients are priority objectives. |
doi_str_mv | 10.1007/s11883-021-00926-3 |
format | article |
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To elucidate the current approach of care in pediatric patients with familial hypercholesterolemia (FH). We sought an answer to the question whether the advances and major changes in lipid management are relevant and apply to children and adolescents.
Recent Findings
Latest research findings clearly demonstrate that lowering cholesterol levels at a young age prevents vascular atherosclerotic changes and decreases cardiovascular events in adulthood and emphasizes the importance of early detection and intervention in the pediatric FH patients group.
Summary
FH is a common genetic disease caused by mutations in genes associated with the metabolism of low-density lipoproteins (LDL). The hallmark of FH is elevated LDL cholesterol (LDL-C) levels from birth and premature atherosclerotic cardiovascular disease (ASCVD). Often FH is either undiagnosed or diagnosed with a considerable delay, leading to vascular atherosclerotic changes and cardiovascular disease. Prompt identification of FH subjects is essential, to initiate early preventive measures. Safe and efficient pharmacological agents are approved for use in children and adolescents. Statins are the first line of therapy, in combination of ezetimibe. Unfortunately, these drugs do not warrant the achievement of therapeutic target, especially in HoFH patient. In the latter, lipoprotein apheresis (LA), which has been shown to be safe and effective, is strongly recommended. Finally, the new drugs still under study will allow a multimodal customized treatment. Lowering cholesterol levels at a young age hinders vascular atherosclerotic changes decreasing cardiovascular events in adulthood. Therefore, early detection, diagnosis, and intervention in FH patients are priority objectives.</description><identifier>ISSN: 1523-3804</identifier><identifier>EISSN: 1534-6242</identifier><identifier>DOI: 10.1007/s11883-021-00926-3</identifier><identifier>PMID: 33963467</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Angiology ; Cardiology ; Medicine ; Medicine & Public Health ; Section Editor ; Statin Drugs (R. Ceska ; Statin Drugs (R. Ceska, Section Editor) ; Topical Collection on Statin Drugs</subject><ispartof>Current atherosclerosis reports, 2021-06, Vol.23 (6), p.30-30, Article 30</ispartof><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-96025556351740c22d9f753a0a11a2f556ffd54afe18148cf1dca4728e5fa7083</citedby><cites>FETCH-LOGICAL-c512t-96025556351740c22d9f753a0a11a2f556ffd54afe18148cf1dca4728e5fa7083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33963467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cohen, Hofit</creatorcontrib><creatorcontrib>Stefanutti, Claudia</creatorcontrib><creatorcontrib>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</creatorcontrib><creatorcontrib>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</creatorcontrib><title>Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents</title><title>Current atherosclerosis reports</title><addtitle>Curr Atheroscler Rep</addtitle><addtitle>Curr Atheroscler Rep</addtitle><description>Purpose of Review
To elucidate the current approach of care in pediatric patients with familial hypercholesterolemia (FH). We sought an answer to the question whether the advances and major changes in lipid management are relevant and apply to children and adolescents.
Recent Findings
Latest research findings clearly demonstrate that lowering cholesterol levels at a young age prevents vascular atherosclerotic changes and decreases cardiovascular events in adulthood and emphasizes the importance of early detection and intervention in the pediatric FH patients group.
Summary
FH is a common genetic disease caused by mutations in genes associated with the metabolism of low-density lipoproteins (LDL). The hallmark of FH is elevated LDL cholesterol (LDL-C) levels from birth and premature atherosclerotic cardiovascular disease (ASCVD). Often FH is either undiagnosed or diagnosed with a considerable delay, leading to vascular atherosclerotic changes and cardiovascular disease. Prompt identification of FH subjects is essential, to initiate early preventive measures. Safe and efficient pharmacological agents are approved for use in children and adolescents. Statins are the first line of therapy, in combination of ezetimibe. Unfortunately, these drugs do not warrant the achievement of therapeutic target, especially in HoFH patient. In the latter, lipoprotein apheresis (LA), which has been shown to be safe and effective, is strongly recommended. Finally, the new drugs still under study will allow a multimodal customized treatment. Lowering cholesterol levels at a young age hinders vascular atherosclerotic changes decreasing cardiovascular events in adulthood. Therefore, early detection, diagnosis, and intervention in FH patients are priority objectives.</description><subject>Angiology</subject><subject>Cardiology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Section Editor</subject><subject>Statin Drugs (R. Ceska</subject><subject>Statin Drugs (R. Ceska, Section Editor)</subject><subject>Topical Collection on Statin Drugs</subject><issn>1523-3804</issn><issn>1534-6242</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kT9PwzAQxS0EolD4AgzII0vA5z-JuyBVhVIkJJYyWyax21RJXOwEqXx6nLZUsDDZ1vvduzs_hK6A3AIh2V0AkJIlhEJCyIimCTtCZyAYT1LK6XF_pyxhkvABOg9hRQglMoVTNGBslDKeZmdoNem8N02Lx-u1dzpf4tbhdmnwQ6kXjQtlwLop8Nwb3dY95yyemdZ497VZuNZs1Zmrt88u4OkMT5ZlVUTPrTQuXGVCHivDBTqxugrmcn8O0dv0cT6ZJS-vT8-T8UuSC6BtMkoJFUKkTEDGSU5pMbKZYJpoAE1tVKwtBNfWgAQucwtFrnlGpRFWZ0SyIbrf-a6799oUfW-vK7X2Za39Rjldqr9KUy7Vwn0qCURQDtHgZm_g3UdnQqvqMq5QVboxcUdFI8XiHNCjdIfm3oXgjT20AaL6kNQuJBVDUtuQFItF178HPJT8pBIBtgNClJqF8WrlOt_ET_vP9hu7ZJ5v</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Cohen, Hofit</creator><creator>Stefanutti, Claudia</creator><general>Springer US</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210601</creationdate><title>Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents</title><author>Cohen, Hofit ; Stefanutti, Claudia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-96025556351740c22d9f753a0a11a2f556ffd54afe18148cf1dca4728e5fa7083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Angiology</topic><topic>Cardiology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Section Editor</topic><topic>Statin Drugs (R. Ceska</topic><topic>Statin Drugs (R. Ceska, Section Editor)</topic><topic>Topical Collection on Statin Drugs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cohen, Hofit</creatorcontrib><creatorcontrib>Stefanutti, Claudia</creatorcontrib><creatorcontrib>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</creatorcontrib><creatorcontrib>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Current atherosclerosis reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cohen, Hofit</au><au>Stefanutti, Claudia</au><aucorp>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</aucorp><aucorp>and The Mighty Medic Satellite Research Group for Pediatric Dyslipidemia</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents</atitle><jtitle>Current atherosclerosis reports</jtitle><stitle>Curr Atheroscler Rep</stitle><addtitle>Curr Atheroscler Rep</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>23</volume><issue>6</issue><spage>30</spage><epage>30</epage><pages>30-30</pages><artnum>30</artnum><issn>1523-3804</issn><eissn>1534-6242</eissn><abstract>Purpose of Review
To elucidate the current approach of care in pediatric patients with familial hypercholesterolemia (FH). We sought an answer to the question whether the advances and major changes in lipid management are relevant and apply to children and adolescents.
Recent Findings
Latest research findings clearly demonstrate that lowering cholesterol levels at a young age prevents vascular atherosclerotic changes and decreases cardiovascular events in adulthood and emphasizes the importance of early detection and intervention in the pediatric FH patients group.
Summary
FH is a common genetic disease caused by mutations in genes associated with the metabolism of low-density lipoproteins (LDL). The hallmark of FH is elevated LDL cholesterol (LDL-C) levels from birth and premature atherosclerotic cardiovascular disease (ASCVD). Often FH is either undiagnosed or diagnosed with a considerable delay, leading to vascular atherosclerotic changes and cardiovascular disease. Prompt identification of FH subjects is essential, to initiate early preventive measures. Safe and efficient pharmacological agents are approved for use in children and adolescents. Statins are the first line of therapy, in combination of ezetimibe. Unfortunately, these drugs do not warrant the achievement of therapeutic target, especially in HoFH patient. In the latter, lipoprotein apheresis (LA), which has been shown to be safe and effective, is strongly recommended. Finally, the new drugs still under study will allow a multimodal customized treatment. Lowering cholesterol levels at a young age hinders vascular atherosclerotic changes decreasing cardiovascular events in adulthood. Therefore, early detection, diagnosis, and intervention in FH patients are priority objectives.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>33963467</pmid><doi>10.1007/s11883-021-00926-3</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | Springer Nature |
subjects | Angiology Cardiology Medicine Medicine & Public Health Section Editor Statin Drugs (R. Ceska Statin Drugs (R. Ceska, Section Editor) Topical Collection on Statin Drugs |
title | Current Approach to the Diagnosis and Treatment of Heterozygote and Homozygous FH Children and Adolescents |
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