Oros Mihaela, Baranga Lucica, Glangher Adelina, Adina-Diana Moldovan, Jugulete Gheorghita, Pavelescu Carmen, Mihaltan Florin, Plaiasu Vasilica, Gheorghe Dan Cristian
Ponderas Academic Hospital, No. 85A, Nicolae G. Caramfil Street, 014142 Bucharest, Romania.
Physiology, Department of Preclinical Sciences, Faculty of Medicine, Titu Maiorescu University, No. 67A, Gheorghe Petrascu Street, 3rd District, 031593 Bucharest, Romania.
J Pers Med. 2023 Nov 4;13(11):1577. doi: 10.3390/jpm13111577.
Collagen VI-related disorders constitute a spectrum of severities from the milder Bethlem myopathy (BM) to the Ullrich congenital muscular dystrophy (UCMD), which is more severe, and an intermediate form characterized by muscle weakness that begins in infancy. Affected children are able to walk, although walking becomes increasingly difficult starting in early adulthood. They develop contractures in the ankles, elbows, knees, and spine in childhood. In some affected cases, the respiratory muscles are weakened, requiring mechanical ventilation, particularly during sleep. Individuals with collagen VI-related myopathy are at risk of restrictive lung disease and sleep-disordered breathing due to the development of scoliosis associated with neuromuscular weakness. Typical signs of respiratory failure are not always present, and some patients are unaware that their respiratory muscles have become weaker. Here, we report a case of an intermediate form of collagen VI-related myopathy confirmed by next-generation sequencing. The girl presented morning headache, irritability, and aggressiveness, and because of these main symptoms, she was referred by the neurologist for respiratory evaluation. The result of spirometry was associated with hypoventilation shown during sleep studies, indicating the necessity to initiate home non-invasive ventilation (NIV) with immediate improvement in the symptoms. Neuromuscular disorders (NMDs) have a great impact on sleep, but only very few studies evaluating sleep quality in young patients with collagen VI-related myopathy have been described. Daytime symptoms of sleep-disordered breathing may include irritability, emotional lability, and poor attentiveness, but these can be overseen by the severity of other complex medical problems in patients with collagen VI-related myopathy. We underline the importance of the close monitoring of respiratory function, sleep evaluation, and decision making to support the NIV treatment of other collagen VI-related myopathy variant-specific patients. Early recognition of sleep disturbances and initiation of respiratory support can preserve or enhance the quality of life for patients and their caregivers. Routine screening for identification of emotional distress should be instituted in the clinical practice using validated psychological measures in a multidisciplinary approach with different intervention strategies for both patient and parent when necessary.
VI型胶原蛋白相关疾病涵盖了从症状较轻的贝思伦肌病(BM)到更为严重的乌尔里希先天性肌营养不良(UCMD)等一系列严重程度不等的病症,还有一种中间型,其特征为婴儿期起病的肌无力。患病儿童能够行走,不过从成年早期开始行走会愈发困难。他们在儿童期会出现脚踝、肘部、膝盖和脊柱的挛缩。在一些患病案例中,呼吸肌会变弱,需要机械通气,尤其是在睡眠期间。VI型胶原蛋白相关肌病患者因与神经肌肉无力相关的脊柱侧弯发展,有患限制性肺病和睡眠呼吸障碍的风险。呼吸衰竭的典型症状并不总是存在,一些患者并未意识到其呼吸肌已经变弱。在此,我们报告一例经下一代测序确诊的VI型胶原蛋白相关肌病中间型病例。该女孩出现晨起头痛、易怒和攻击性,由于这些主要症状,神经科医生将她转诊进行呼吸评估。肺活量测定结果与睡眠研究中显示的通气不足相关,表明有必要启动家庭无创通气(NIV),症状随即得到改善。神经肌肉疾病(NMDs)对睡眠有很大影响,但仅有极少数评估VI型胶原蛋白相关肌病年轻患者睡眠质量的研究被报道。睡眠呼吸障碍的日间症状可能包括易怒、情绪不稳定和注意力不集中,但这些可能会被VI型胶原蛋白相关肌病患者其他复杂医疗问题的严重程度所掩盖。我们强调密切监测呼吸功能、进行睡眠评估以及做出决策以支持对其他VI型胶原蛋白相关肌病特定变体患者进行NIV治疗的重要性。早期识别睡眠障碍并启动呼吸支持可以维持或提高患者及其照料者的生活质量。在临床实践中应采用经过验证的心理测量方法,通过多学科方法进行常规筛查以识别情绪困扰,必要时针对患者和家长采用不同的干预策略。