Pederiva Cristina, Galimberti Federica, Casula Manuela, Banderali Giuseppe, Beccuti Guglielmo, Bianconi Vanessa, Biasucci Giacomo, Biolo Marta, Bucci Marco, Buonuomo Paola Sabrina, Calabrò Paolo, Carugo Stefano, Cefalù Angelo Baldassare, Citroni Nadia, Cocomello Nicholas, D'Addato Sergio, Gatti Simona, Genovesi Simonetta, Guardamagna Ornella, Iannuzzo Gabriella, Iughetti Lorenzo, Mandraffino Giuseppe, Maroni Lorenzo, Minicocci Ilenia, Mombelli Giuliana, Montalcini Tiziana, Moriglia Sara, Muntoni Sandro, Nascimbeni Fabio, Passaro Angelina, Pellegatta Fabio, Pisciotta Livia, Sani Elena, Sbrana Francesco, Scicali Roberto, Suppressa Patrizia, Werba José Pablo, Zenti Maria Grazia, Arca Marcello, Averna Maurizio, Calandra Sebastiano, Catapano Alberico Luigi, Tarugi Patrizia, Capra Maria Elena
Clinical Service for Dyslipidaemias, Study and Prevention of Atherosclerosis in Childhood, Paediatrics Unit, ASST-Santi Paolo e Carlo, 20142 Milan, Italy.
IRCCS MultiMedica, 20099 Sesto San Giovanni, Italy.
Children (Basel). 2025 Feb 26;12(3):288. doi: 10.3390/children12030288.
Awareness, diagnosis, and treatment of familial hypercholesterolemia (FH) starting from childhood are a cornerstone of cardiovascular disease prevention. The LIPIGEN Paediatric Group, a network of specialised centres for the diagnosis and management of familial genetic dyslipidemia, is an active part of this mission.
This is the second exploratory survey organised within the LIPIGEN (LIpid transPort disorders Italian GEnetic Network) paediatric centres. A digital questionnaire consisting of 16 questions was proposed to the principal investigators of 35 LIPIGEN centres in September 2023. We analysed the main FH screening strategies implemented in Italy, which are the referral characteristics to the lipid clinics and clinical and biochemical criteria considered to diagnose FH in paediatric patients.
Centres frequently reported conducting cascade screening (88.6%) and reverse screening (57.1%), whereas 28.6% of respondents indicated using selective screening and only 5.7% reported employing child-parent screening. We documented a detailed biochemical characterisation of paediatric patients (62.9% of respondents usually perform full lipoprotein profile and 80% determine lipoprotein(a) for each patient) and a high percentage of genetic analysis (82.9%). We have also highlighted a quite low awareness of FH as a genetic condition involving paediatric patients among primary care paediatricians and general practitioners.
The results of our survey show that specialised lipid centres usually have good diagnostic competence when dealing with paediatric patients with hypercholesterolemia. However, FH awareness and the importance of early diagnosis and treatment initiation in childhood still need to be further improved.
从儿童期开始对家族性高胆固醇血症(FH)进行认知、诊断和治疗是心血管疾病预防的基石。LIPIGEN儿科小组是一个由家族性遗传性血脂异常诊断和管理专业中心组成的网络,是这一使命的积极参与者。
这是在LIPIGEN(意大利脂质转运障碍遗传网络)儿科中心组织的第二次探索性调查。2023年9月,向35个LIPIGEN中心的主要研究人员发放了一份包含16个问题的数字问卷。我们分析了意大利实施的主要FH筛查策略,即转诊至血脂门诊的特征以及用于诊断儿科患者FH的临床和生化标准。
各中心经常报告进行级联筛查(88.6%)和反向筛查(57.1%),而28.6%的受访者表示采用选择性筛查,只有5.7%报告采用儿童-父母筛查。我们记录了儿科患者详细的生化特征(62.9%的受访者通常进行完整的脂蛋白谱分析,80%为每位患者测定脂蛋白(a))以及高比例的基因分析(82.9%)。我们还强调,初级保健儿科医生和全科医生对FH作为一种涉及儿科患者的遗传疾病的认知相当低。
我们的调查结果表明,在处理高胆固醇血症的儿科患者时,专业血脂中心通常具有良好的诊断能力。然而,FH的认知以及儿童早期诊断和开始治疗的重要性仍需进一步提高。