Department of Pharmacy, University of Pisa, 56120 Pisa, Italy.
Fondazione Italiana Ricerca Sulle Malattie dell'Osso (FIRMO Onlus), 50129 Florence, Italy.
Nutrients. 2024 May 23;16(11):1576. doi: 10.3390/nu16111576.
Multiple endocrine neoplasia type 1 (MEN1) is a rare syndrome caused by inactivating mutations in the MEN1 tumor suppressor gene. The three main clinical manifestations of MEN1 are primary hyperparathyroidism (PHPT), duodenal-pancreatic neuroendocrine tumors (DP-NETs) and anterior pituitary tumors. Endocrine tumors in patients with MEN1 differ from sporadic tumors because of their younger age at onset, common multiple presentations and the different clinical course. MEN1 is characterized by a complex clinical phenotype; thus, patients should be followed by a multidisciplinary team of experts that includes an endocrinologist, a surgeon, a oncologist, a radiotherapist, and not least, a nutritionist. It is important to remember the fundamental role that diet plays as a primary prevention tool, together with a healthy and active lifestyle in preventing osteoporosis/osteopenia and reducing the risk of developing kidney stones due to hypercalciuria, two frequent clinical complications in MEN1 patients. Is very important for MEN1 patients to have an adequate intake of calcium, vitamin D, magnesium and phosphate to maintain good bone health. The intake of foods containing oxalates must also be kept under control because in combination with calcium they concur to form calcium oxalate crystals, increasing the risk of nephrolithiasis. Another aspect to consider is the management of patients with pancreatic neuroendocrine tumors undergoing major surgical resections of the pancreas that can lead to alterations in digestion and absorption mechanisms due to partial or total reduction in pancreatic enzymes such as amylase, lipase, and protease, resulting in malabsorption and malnutrition. Therefore, the nutritionist's aim should be to devise a dietary plan that takes into consideration each single patient, educating them about a healthy and active lifestyle, and accompanying them through various life stages by implementing strategies that can enhance their quality of life.
多发性内分泌腺瘤病 1 型(MEN1)是一种罕见的综合征,由 MEN1 肿瘤抑制基因失活突变引起。MEN1 的三个主要临床表现是原发性甲状旁腺功能亢进症(PHPT)、十二指肠-胰腺神经内分泌肿瘤(DP-NET)和垂体前叶肿瘤。MEN1 患者的内分泌肿瘤与散发性肿瘤不同,因为它们的发病年龄更小、常见多发表现和不同的临床过程。MEN1 的特征是复杂的临床表型;因此,患者应由内分泌学家、外科医生、肿瘤学家、放射治疗师和营养师等多学科专家团队进行随访。重要的是要记住,饮食作为主要预防工具以及健康积极的生活方式在预防骨质疏松症/低骨量症和降低因高钙尿症导致肾结石风险方面发挥着重要作用,这是 MEN1 患者的两个常见临床并发症。MEN1 患者摄入足够的钙、维生素 D、镁和磷酸盐以维持良好的骨骼健康非常重要。还必须控制含草酸盐食物的摄入,因为它们与钙结合会形成草酸钙晶体,增加肾结石的风险。另一个需要考虑的方面是管理接受胰腺神经内分泌肿瘤大切除术的患者,这些手术会导致消化和吸收机制发生变化,因为胰腺酶(如淀粉酶、脂肪酶和蛋白酶)的部分或全部减少,导致吸收不良和营养不良。因此,营养师的目标应该是制定一个考虑到每个患者的饮食计划,教育他们健康积极的生活方式,并通过实施可以提高他们生活质量的策略来陪伴他们度过各个生命阶段。