» Articles » PMID: 25727906

Postural Vital Capacity Difference with Aging in Duchenne Muscular Dystrophy

Overview
Journal Muscle Nerve
Date 2015 Mar 3
PMID 25727906
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: A change in vital capacity (VC) from standing to supine can be an index of diaphragm paralysis if it exceeds 25%. We aimed to verify whether the postural VC difference increases with age and reflects diaphragm weakness in DMD.

Methods: VCs were measured in DMD. Postural VC difference and percentage were calculated from the VC data. Maximal inspiratory pressure (MIP) and MIP percentage were measured as an indirect index of diaphragm weakness.

Results: A total of 220 patients and 544 measurements were collected. MIP and MIP percentage decreased significantly with age (P < 0.001 for both). Estimated postural VC difference and percentage also decreased (P < 0.001, P = 0.006, respectively). Age group comparisons showed a significant decrease in younger, but not older subjects.

Conclusions: This study shows that the postural VC difference tended to decrease with age and might not reflect diaphragmatic weakness in DMD; however, this should be interpreted cautiously.

Citing Articles

Unveiling the Respiratory Muscle Strength in Duchenne Muscular Dystrophy: The Impact of Nutrition and Thoracic Deformities, Beyond Spirometry.

Yuksel Kalyoncu M, Gokdemir Y, Yilmaz Yegit C, Yanaz M, Gulieva A, Selcuk M Children (Basel). 2024; 11(8).

PMID: 39201929 PMC: 11352812. DOI: 10.3390/children11080994.


Clinical implication of maximal voluntary ventilation in myotonic muscular dystrophy.

Suh M, Kim D, Jung J, Kim B, Lee J, Choi W Medicine (Baltimore). 2019; 98(18):e15321.

PMID: 31045770 PMC: 6504256. DOI: 10.1097/MD.0000000000015321.


Respiratory magnetic resonance imaging biomarkers in Duchenne muscular dystrophy.

Mankodi A, Kovacs W, Norato G, Hsieh N, Bandettini W, Bishop C Ann Clin Transl Neurol. 2017; 4(9):655-662.

PMID: 28904987 PMC: 5590523. DOI: 10.1002/acn3.440.


Assessment and management of respiratory function in patients with Duchenne muscular dystrophy: current and emerging options.

LoMauro A, DAngelo M, Aliverti A Ther Clin Risk Manag. 2015; 11:1475-88.

PMID: 26451113 PMC: 4592047. DOI: 10.2147/TCRM.S55889.