Couce María Luz, Sánchez-Pintos Paula, Aldámiz-Echevarría Luís, Vitoria Isidro, Navas Victor, Martín-Hernández Elena, García-Volpe Camila, Pintos Guillem, Peña-Quintana Luis, Hernández Tomás, Gil David, Sánchez-Valverde Félix, Bueno María, Roca Iria, López-Ruzafa Encarna, Díaz-Fernández Carmen
Unit of Diagnosis and Treatment of Congenital Metabolic Diseases, S. Neonatology, Department of Pediatrics, Clínico Universitario de Santiago de Compostela, CIBERER, Health Research Institute of Santiago de Compostela (IDIS).
Unit of Metabolism, Department of Pediatrics, Hospital de Cruces, Group of Metabolism, Biocruces Health Research Institute, CIBERER.
Medicine (Baltimore). 2019 Sep;98(39):e17303. doi: 10.1097/MD.0000000000017303.
Treatment with nitisinone (NTBC) has brought about a drastic improvement in the treatment and prognosis of hereditary tyrosinemia type I (HT1). We conducted a retrospective observational multicentric study in Spanish HT1 patients treated with NTBC to assess clinical and biochemical long-term evolution.We evaluated 52 patients, 7 adults and 45 children, treated with NTBC considering: age at diagnosis, diagnosis by clinical symptoms, or by newborn screening (NBS); phenotype (acute/subacute/chronic), mutational analysis; symptoms at diagnosis and clinical course; biochemical markers; doses of NTBC; treatment adherence; anthropometric evolution; and neurocognitive outcome.The average follow-up period was 6.1 ± 4.9 and 10.6 ± 5.4 years in patients with early and late diagnosis respectively. All patients received NTBC from diagnosis with an average dose of 0.82 mg/kg/d. All NBS-patients (n = 8) were asymptomatic at diagnosis except 1 case with acute liver failure, and all remain free of liver and renal disease in follow-up. Liver and renal affectation was markedly more frequent at diagnosis in patients with late diagnosis (P < .001 and .03, respectively), with ulterior positive hepatic and renal course in 86.4% and 93.2% of no-NBS patients, although 1 patient with good metabolic control developed hepatocarcinoma.Despite a satisfactory global nutritional evolution, 46.1% of patients showed overweight/obesity. Interestingly lower body mass index was observed in patients with good dietary adherence (20.40 ± 4.43 vs 24.30 ± 6.10; P = .08) and those with good pharmacological adherence (21.19 ± 4.68 vs 28.58 ± 213.79).intellectual quotient was ≥85 in all NBS- and 68.75% of late diagnosis cases evaluated, 15% of which need pedagogical support, and 6.8% (3/44) showed school failure.Among the 12 variants identified in fumarylacetoacetate hydrolase gene, 1 of them novel (H63D), the most prevalent in Spanish population is c.554-1 G>T.After NTBC treatment a reduction in tyrosine and alpha-fetoprotein levels was observed in all the study groups, significant for alpha-fetoprotein in no NBS-group (P = .03), especially in subacute/chronic forms (P = .018).This series confirms that NTBC treatment had clearly improved the prognosis and quality of life of HT1 patients, but it also shows frequent cognitive dysfunctions and learning difficulties in medium-term follow-up, and, in a novel way, a high percentage of overweight/obesity.
用尼替西农(NTBC)治疗已使1型遗传性酪氨酸血症(HT1)的治疗和预后得到显著改善。我们对接受NTBC治疗的西班牙HT1患者进行了一项回顾性观察性多中心研究,以评估临床和生化方面的长期演变。我们评估了52例接受NTBC治疗的患者,其中7例为成人,45例为儿童,考虑因素包括:诊断时的年龄、通过临床症状或新生儿筛查(NBS)进行的诊断;表型(急性/亚急性/慢性)、突变分析;诊断时的症状和临床病程;生化标志物;NTBC的剂量;治疗依从性;人体测量学演变;以及神经认知结果。早期诊断和晚期诊断患者的平均随访期分别为6.1±4.9年和10.6±5.4年。所有患者自诊断起均接受NTBC治疗,平均剂量为0.82mg/kg/d。所有通过NBS诊断的患者(n = 8)在诊断时均无症状,仅1例患有急性肝衰竭,且所有患者在随访中均未出现肝脏和肾脏疾病。晚期诊断患者在诊断时肝脏和肾脏受累明显更为频繁(分别为P <.001和.03),尽管1例代谢控制良好的患者发生了肝癌,但86.4%的非NBS患者肝脏和93.2%的非NBS患者肾脏病情随后呈阳性转归。尽管总体营养状况演变令人满意,但46.1%的患者出现超重/肥胖。有趣的是,饮食依从性良好的患者(20.40±4.43 vs 24.30±6.10;P = 0.08)和药物依从性良好的患者(21.19±4.68 vs 28.58±213.79)的体重指数较低。在所有接受评估的通过NBS诊断的患者以及68.75%的晚期诊断病例中,智商≥85,其中15%的患者需要教育支持,6.8%(3/44)的患者出现学业失败。在富马酰乙酰乙酸水解酶基因中鉴定出的12种变异中,有1种是新变异(H63D),在西班牙人群中最常见的是c.554-1 G>T。在NTBC治疗后,所有研究组的酪氨酸和甲胎蛋白水平均有所降低,非NBS组中甲胎蛋白水平降低具有显著性(P = 0.03),尤其是在亚急性/慢性形式中(P = 0.018)。该系列研究证实,NTBC治疗明显改善了HT1患者的预后和生活质量,但也显示出在中期随访中频繁出现认知功能障碍和学习困难,并且,以一种新的方式,超重/肥胖的比例很高。