Pediatrics cascade screening in inherited dyslipidemias: a lipoprotein apheresis center experience.

IF 3.7 3区 医学 Q2 Medicine Endocrine Pub Date : 2024-12-24 DOI:10.1007/s12020-024-04144-0
Francesco Sbrana, Beatrice Dal Pino, Carmen Corciulo, Andrea Ripoli, Federico Bigazzi, Tiziana Sampietro
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Abstract

Familial hypercholesterolemia (FH) is less rare than one might think and, despite highly effective lipid-lowering therapies (LLT), more than half of the patients treated do not reach the lipid target indicated by the guidelines. In these patients, lipoprotein apheresis (LA) is the most effective tool to lowering apo-B containing atherogenic lipoproteins. In own center, since 1994, thanks to routinely cascade testing performed in patients who start LA, we have identified a pediatric population (30 subjects) that we analyzed retrospectively. Cascade screening, performed in subject with premature cardiovascular events or inherited dyslipidemias, is an effective approach to identified pediatric FH, a condition that pediatricians should also be aware. A dedicate network is required to investigate the involved genetic mutations and to set up a management program, including lipoprotein (a) measurement and subclinical atherosclerosis evaluation. Moreover, it is important that medical staff use a therapeutic pathway to help patients overcome discomfort associated with disease and chronic LLT, as well as improve adherence to lipid-lowering drugs.

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遗传性血脂异常的儿科级联筛查:脂蛋白分离中心的经验。
家族性高胆固醇血症(FH)并不像人们想象的那么罕见,尽管有高效的降脂疗法(LLT),但超过一半的接受治疗的患者没有达到指南规定的血脂目标。在这些患者中,脂蛋白分离(LA)是降低含载脂蛋白b的致动脉粥样硬化脂蛋白的最有效工具。在本中心,自1994年以来,由于对开始LA治疗的患者进行了常规级联试验,我们确定了一个儿科人群(30名受试者),并对其进行了回顾性分析。在有过早心血管事件或遗传性血脂异常的受试者中进行级联筛查,是识别儿童FH的有效方法,儿科医生也应该意识到这一点。需要一个专门的网络来调查相关的基因突变,并建立一个管理程序,包括脂蛋白(A)测量和亚临床动脉粥样硬化评估。此外,重要的是医务人员使用治疗途径来帮助患者克服与疾病和慢性LLT相关的不适,并提高对降脂药物的依从性。
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来源期刊
Endocrine
Endocrine 医学-内分泌学与代谢
CiteScore
6.40
自引率
5.40%
发文量
0
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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