一个希腊阿贝塔利蛋白血症家族33年随访:长期补充中链甘油三酯无肝损害

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
John K Triantafillidis, Areti Manioti, Theodoros Pittaras, Theodoros Kozonis, Emmanouil Kritsotakis, Georgios Malgarinos, Konstantinos Pantos, Konstantinos Sfakianoudis, Manousos M Konstadoulakis, Apostolos E Papalois
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引用次数: 0

摘要

背景:描述了对一个希腊ABL家族进行33年随访的长期临床和实验室结果。病例报告:患者(兄弟姐妹二人,年龄分别为57岁、49岁和62岁)仍活着,正在密切监测中。三名患者中有两名腹泻出现在婴儿期早期,而第三名出现在青春期。中枢神经系统症状在第二个十年后恶化。与此同时,夜盲症出现在疾病的晚期,导致一名男性患者几乎完全丧失视力,另一名患者严重受损。诊断是基于临床表现,眼科检查结果,血脂估计,周围棘细胞增多症的存在。所有患者均表现出典型的血脂特征、眼科检查结果和外周血棘细胞。在随访期间,严格调整饮食,包括用中链甘油三酯(MCT油)代替脂肪。自最初诊断33年后,尽管持续使用MCT油,所有患者都没有任何肝功能障碍的迹象。然而,中枢神经系统和视力受损的症状恶化了。结论:这些患者的病程表明,应用改良饮食,包括MCT油,并密切监测,可以延长患者的生存期,无明显的肝脏副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thirty-Three Years Follow-Up of a Greek Family with Abetalipoproteinemia: Absence of Liver Damage on Long-Term Medium Chain Triglycerides Supplementation.

Thirty-Three Years Follow-Up of a Greek Family with Abetalipoproteinemia: Absence of Liver Damage on Long-Term Medium Chain Triglycerides Supplementation.

Thirty-Three Years Follow-Up of a Greek Family with Abetalipoproteinemia: Absence of Liver Damage on Long-Term Medium Chain Triglycerides Supplementation.

Thirty-Three Years Follow-Up of a Greek Family with Abetalipoproteinemia: Absence of Liver Damage on Long-Term Medium Chain Triglycerides Supplementation.

Background: The long-term clinical and laboratory results of a 33-year follow-up of a Greek family with abetalipoproteinemia (ABL) are described. Case Report: The patients (two brothers and their sister, aged 57, 49, and 62 years, respectively) are still alive, being under close surveillance. In two of the three patients, diarrhea appeared in early infancy, while in the third, it appeared during adolescence. CNS symptomatology worsened after the second decade of life. At the same time, night blindness appeared in the advanced stages of the disease, resulting in almost complete loss of vision in one of the male patients and severe impairment in the other. The diagnosis was based on the clinical picture, ophthalmological findings, serum lipid estimations, and presence of peripheral acanthocytosis. All patients exhibited typical serum lipidemic profile, ophthalmological findings, and acanthocytes in the peripheral blood. During the follow-up period, strict dietary modifications were applied, including the substitution of fat with medium-chain triglycerides (MCT oil). After 33 years since the initial diagnosis, all patients are alive without any sign of liver dysfunction despite continuous use of MCT oil. However, symptoms from the central nervous system and vision impairment worsened. Conclusion: The course of these patients suggests that the application of a modified diet, including MCT oil, along with close surveillance, could prolong the survival of patients without significant side effects from the liver.

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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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