Suppr超能文献

通过新生儿筛查确诊的晚发型庞贝病患者的肌肉超声检查

Muscle ultrasound in patients with late-onset Pompe disease identified by newborn screening.

作者信息

Jackson David G, Case Laura E, Huggins Erin, Holland Maggie, Blount Janet, Webb Lisa Hobson, Kishnani Priya S

机构信息

Division of Medical Genetics, Duke University Medical Center, Durham, NC, USA.

Doctor of Physical Therapy Division, Duke University Medical Center, Durham, NC, USA.

出版信息

Mol Genet Metab Rep. 2023 Jul 5;36:100989. doi: 10.1016/j.ymgmr.2023.100989. eCollection 2023 Sep.

Abstract

IMPORTANCE

Implementation of newborn screening (NBS) in the United States now detects infants with late-onset Pompe disease (LOPD), a lysosomal storage disease characterized by slowly progressive muscle weakness, and detailed clinical evaluation has identified early muscle weakness. Biomarkers may be uninformative; thus, non-invasive imaging is needed to assess early LOPD muscle changes. Muscle ultrasound (US) measuring echointensity (EI) is a non-invasive measure of muscle health.

OBJECTIVE

In this study, we aimed to evaluate if EI can identify characteristic patterns of muscle involvement in LOPD patients identified by NBS.

DESIGN/SETTING: Prospective, cross-sectional, single time point study.

SETTING

One-center study.

PARTICIPANTS

We examined 20 infants with NBS-identified LOPD (ages 5-20 months). All had standardized physical therapy assessments.

EXPOSURES

Creatine Kinase (CK) and Urine Hexose Tetrasaccharide (Glc4) were obtained. Muscle US of deltoid, biceps brachii, forearm flexors, thoracic paraspinals, gluteus maximus, quadriceps, tibialis anterior and medial gastrocnemius was performed.

MAIN OUTCOMES AND MEASURES

Mean EI was calculated for all involved muscle groups. Quantitative EI Sum Scores were calculated as total EI divided by number of muscle groups assessed. We performed a comprehensive literature review to compare our results to previous LOPD muscle ultrasound studies.

RESULTS

Six of 20 participants had elevated CK and 15 had 50% of the most common concerning kinematic physical findings; with normal urine Glc4 in all except one. Based upon muscle EI, the most affected muscles were quadriceps and medial gastrocnemius, with notable elevated EI in thoracic paraspinals. Biceps brachii was the most frequently affected upper extremity muscle. EI sum scores correlated moderately with increasing CK. Statistically significant positive correlation was found between posterior pelvic tilt in sitting and EI of gluteus maximus. Sonographic pattern of muscle involvement was similar to previous studies assessing older patients with LOPD.

CONCLUSIONS AND RELEVANCE

In this study, muscle EI was elevated most often in the quadriceps, tibialis anterior, medial gastrocnemius, thoracic paraspinals, and biceps brachii. Involved muscles generally fit the profile of physical and muscle ultrasound/MRI exam findings in LOPD patients. Muscle ultrasound is recommended for rapid, focused muscle assessment in LOPD, especially those identified via NBS. Future studies should focus on this pattern of ultrasonographic abnormality and changes over time.

摘要

重要性

美国实施的新生儿筛查(NBS)现已能检测出患有晚发型庞贝病(LOPD)的婴儿,这是一种溶酶体贮积病,其特征为肌肉无力缓慢进展,详细的临床评估已发现早期肌肉无力。生物标志物可能并无信息价值;因此,需要非侵入性成像来评估LOPD早期的肌肉变化。测量回声强度(EI)的肌肉超声(US)是一种评估肌肉健康的非侵入性方法。

目的

在本研究中,我们旨在评估EI是否能识别通过NBS确诊的LOPD患者的特征性肌肉受累模式。

设计/地点:前瞻性、横断面、单时间点研究。

地点

单中心研究。

参与者

我们检查了20名经NBS确诊为LOPD的婴儿(年龄5 - 20个月)。所有婴儿均接受了标准化的物理治疗评估。

暴露因素

获取肌酸激酶(CK)和尿己糖四糖(Glc4)。对三角肌、肱二头肌、前臂屈肌、胸段椎旁肌、臀大肌、股四头肌、胫前肌和腓肠内侧肌进行肌肉超声检查。

主要结局和测量指标

计算所有受累肌肉群的平均EI。定量EI总和评分计算为总EI除以评估的肌肉群数量。我们进行了全面的文献综述,以将我们的结果与先前关于LOPD肌肉超声的研究进行比较。

结果

20名参与者中有6人CK升高,15人有50%最常见的相关运动物理检查异常;除1人外,所有人的尿Glc4均正常。基于肌肉EI,受影响最严重的肌肉是股四头肌和腓肠内侧肌,胸段椎旁肌的EI显著升高。肱二头肌是上肢最常受累的肌肉。EI总和评分与CK升高呈中度相关。在坐位时后骨盆倾斜与臀大肌EI之间发现有统计学意义的正相关。肌肉受累的超声图像模式与先前评估年龄较大的LOPD患者的研究相似。

结论及相关性

在本研究中,股四头肌、胫前肌、腓肠内侧肌、胸段椎旁肌和肱二头肌的肌肉EI最常升高。受累肌肉通常符合LOPD患者的体格检查和肌肉超声/MRI检查结果特征。建议对LOPD患者,尤其是通过NBS确诊的患者,使用肌肉超声进行快速、针对性的肌肉评估。未来的研究应关注这种超声异常模式及其随时间的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c703/10475841/cfb504ff8509/gr1.jpg

相似文献

1
Muscle ultrasound in patients with late-onset Pompe disease identified by newborn screening.
Mol Genet Metab Rep. 2023 Jul 5;36:100989. doi: 10.1016/j.ymgmr.2023.100989. eCollection 2023 Sep.
2
Newborn screening for Pompe disease in Italy: Long-term results and future challenges.
Mol Genet Metab Rep. 2022 Oct 22;33:100929. doi: 10.1016/j.ymgmr.2022.100929. eCollection 2022 Dec.
6
Tongue weakness and atrophy differentiates late-onset Pompe disease from other forms of acquired/hereditary myopathy.
Mol Genet Metab. 2021 Jul;133(3):261-268. doi: 10.1016/j.ymgme.2021.05.005. Epub 2021 May 13.
7
Health care practitioners' experience-based opinions on providing care after a positive newborn screen for Pompe disease.
Mol Genet Metab. 2021 Sep-Oct;134(1-2):20-28. doi: 10.1016/j.ymgme.2021.09.001. Epub 2021 Sep 15.
8
Early clinical phenotype of late onset Pompe disease: Lessons learned from newborn screening.
Mol Genet Metab. 2022 Mar;135(3):179-185. doi: 10.1016/j.ymgme.2022.01.003. Epub 2022 Jan 23.
9
Safety and efficacy of short- and long-term inspiratory muscle training in late-onset Pompe disease (LOPD): a pilot study.
J Neurol. 2019 Jan;266(1):133-147. doi: 10.1007/s00415-018-9112-4. Epub 2018 Nov 14.
10
Whole-body magnetic resonance imaging in late-onset Pompe disease: Clinical utility and correlation with functional measures.
J Inherit Metab Dis. 2020 May;43(3):549-557. doi: 10.1002/jimd.12190. Epub 2019 Nov 26.

引用本文的文献

1
Novel transferrin receptor-mediated enzyme replacement therapy efficiently treats myogenic and neurogenic aspects of Pompe disease in mice.
Mol Ther Methods Clin Dev. 2025 Aug 7;33(3):101547. doi: 10.1016/j.omtm.2025.101547. eCollection 2025 Sep 11.
2
Muscle ultrasound in myopathies.
Curr Opin Neurol. 2024 Oct 1;37(5):549-557. doi: 10.1097/WCO.0000000000001306. Epub 2024 Jul 25.

本文引用的文献

1
Sonographic evaluations of the skeletal muscles in patients with Pompe disease.
Eur J Paediatr Neurol. 2023 Jan;42:22-27. doi: 10.1016/j.ejpn.2022.12.002. Epub 2022 Dec 6.
2
Ultrasonography of abdominal muscles: Differential diagnosis of late-onset Pompe disease and myotonic dystrophy type 1.
Front Neurol. 2022 Sep 6;13:944464. doi: 10.3389/fneur.2022.944464. eCollection 2022.
3
Early clinical phenotype of late onset Pompe disease: Lessons learned from newborn screening.
Mol Genet Metab. 2022 Mar;135(3):179-185. doi: 10.1016/j.ymgme.2022.01.003. Epub 2022 Jan 23.
4
Respiratory Muscle Function Tests and Diaphragm Ultrasound Predict Nocturnal Hypoventilation in Slowly Progressive Myopathies.
Front Neurol. 2021 Oct 14;12:731865. doi: 10.3389/fneur.2021.731865. eCollection 2021.
6
Tongue weakness and atrophy differentiates late-onset Pompe disease from other forms of acquired/hereditary myopathy.
Mol Genet Metab. 2021 Jul;133(3):261-268. doi: 10.1016/j.ymgme.2021.05.005. Epub 2021 May 13.
9
M Mode Ultrasound and Tissue Doppler Imaging to Assess Diaphragm Feature in Late Onset Pompe Disease.
Neurol Int. 2020 Nov 13;12(3):55-58. doi: 10.3390/neurolint12030012.
10
Ultrasound assessment of diaphragm function in patients with late-onset Pompe disease.
Neurol Sci. 2020 Aug;41(8):2175-2184. doi: 10.1007/s10072-020-04316-6. Epub 2020 Mar 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验