Nutritional status of patients with nemaline myopathy and related congenital myopathies in Finland: A pilot study.

IF 3.4 4区 医学 Q2 CLINICAL NEUROLOGY Journal of neuromuscular diseases Pub Date : 2025-01-01 DOI:10.1177/22143602241303374
Vilma-Lotta Lehtokari, Minna Similä, Marianne Tammepuu, Pirjo Isohanni, Mari Auranen, Sinikka Hiekkala, Carina Wallgren-Pettersson, Sonja Strang-Karlsson
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Abstract

Background: The muscle weakness in patients with nemaline myopathy (NM) and related disorders (NMR) often affects the muscles used for eating and dining, and some scientific evidence of poorer nutritional status of patients with myopathy exists. However, comprehensive research on the nutritional status of persons with NM or NMR has not been done.

Objectives: Our aim was to conduct a comprehensive cross-sectional pilot study among adult Finnish patients with NM or NMR to investigate their food consumption, nutrient intakes, selected nutrient-related laboratory parameters in blood, and self-assessed functioning of dining and eating and of the gastrointestinal tract. We also aimed to test the suitability of the methods selected.

Methods: The methods included a questionnaire to investigate eating-related functioning, a food frequency questionnaire, food records, and laboratory analyses from blood samples.

Results: Of 32 invited patients, 20 returned the survey and food frequency questionnaire. Food records were returned by 17, and blood samples were obtained from 16. Food consumption as well as nutrient and energy intake were highly variable between the individuals. Low energy intakes, low consumption of healthy foods, such as fruits, vegetables, and whole grains as well as low intakes of vitamin D, calcium, dietary fiber, vitamin C, folate, and iron were observed. Low nutrient intakes were seen especially in non-ambulatory participants, who also reported challenges in eating and dining related functioning. The laboratory parameters did not indicate severe undernourishment in any of the participants.

Conclusions: Evaluation of food consumption and nutrient intakes were needed to find patients with risk of undernourishment. The results underline the importance of monitoring adequate intake of calcium and vitamin D in this group of patients, especially because of the immobility-induced risk of osteoporosis. Non-ambulatory patients reported more challenges in eating and dining. This, however, did not determine the nutritional status of the patient.

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芬兰线状肌病和相关先天性肌病患者的营养状况:一项初步研究。
背景:线状肌病(NM)及相关疾病(NMR)患者的肌肉无力经常影响用于进食和用餐的肌肉,并且存在一些科学证据表明肌病患者营养状况较差。然而,对核磁共振或核磁共振患者的营养状况尚未进行全面的研究。目的:我们的目的是在芬兰成年NM或NMR患者中进行一项全面的横断面试点研究,调查他们的食物消费、营养摄入、血液中选定的营养相关实验室参数,以及自我评估的饮食功能和胃肠道功能。我们还旨在测试所选方法的适用性。方法:采用进食相关功能调查问卷、进食频率调查问卷、进食记录和血液样本的实验室分析。结果:32例入选患者中,有20例患者返回了调查问卷和饮食频率问卷。其中17人返回了食物记录,16人获得了血液样本。个体之间的食物消耗以及营养和能量摄入差异很大。低能量摄入,低健康食品,如水果、蔬菜和全谷物,以及低维生素D、钙、膳食纤维、维生素C、叶酸和铁的摄入量。营养摄入量低,尤其是在不活动的参与者中,他们也报告了饮食和用餐相关功能的挑战。实验参数没有显示任何参与者存在严重的营养不良。结论:需要评估食物消费和营养摄入,以发现有营养不良风险的患者。研究结果强调了监测这组患者钙和维生素D摄入量的重要性,特别是因为不动导致骨质疏松症的风险。非门诊患者报告在饮食方面有更多的挑战。然而,这并不能确定患者的营养状况。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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