TY - JOUR
T1 - Performance of upper limb entry item to predict forced vital capacity in dysferlin-deficient limb girdle muscular dystrophy
AU - Borland, Holly
AU - Moore, Ursula
AU - Dressman, Heather Gordish
AU - Human, Anri
AU - Mayhew, Anna G.
AU - Hilsden, Heather
AU - Rufibach, Laura E.
AU - Duong, Tina
AU - Maron, Elke
AU - DeWolf, Brittney
AU - Rose, Kristy
AU - Siener, Catherine
AU - Thiele, Simone
AU - Práxedes, Nieves Sanchez Aguilera
AU - Canal, Aurélie
AU - Holsten, Scott
AU - Sakamoto, Chikako
AU - Pedrosa-Hernández, Irene
AU - Bello, Luca
AU - Alfano, Lindsay N.
AU - Lowes, Linda Pax
AU - James, Meredith K.
AU - Straub, Volker
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/10
Y1 - 2024/10
N2 - Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of <60 %, suggestive of respiratory impairment. By contrast, only 10 % of the remainder of the cohort (PUL entry item of 2 or more) had an FVC of <60 %. This relationship also held true when accounting for ambulatory status, age, and sex as possible confounding factors. In summary, our results suggest that the PUL entry item could be implemented in clinical practice to screen for respiratory impairment where spirometry is not readily available.
AB - Dysferlin-deficient limb girdle muscular dystrophy (LGMD R2), also referred to as dysferlinopathy, can be associated with respiratory muscle weakness as the disease progresses. Clinical practice guidelines recommend biennial lung function assessments in patients with dysferlinopathy to screen for respiratory impairment. However, lack of universal access to spirometry equipment and trained specialists makes regular monitoring challenging. This study investigated the use of the Performance of Upper Limb (PUL) clinical scale entry item as a low-cost screening tool to identify patients with dysferlinopathy at risk of respiratory impairment. Using data from 193 patients from the Jain Foundation's International Clinical Outcomes Study, modelling identified a significant positive relationship between the PUL entry item and forced vital capacity (FVC). Eighty-eight percent of patients with the lowest PUL entry item score of 1 presented with FVC % predicted values of <60 %, suggestive of respiratory impairment. By contrast, only 10 % of the remainder of the cohort (PUL entry item of 2 or more) had an FVC of <60 %. This relationship also held true when accounting for ambulatory status, age, and sex as possible confounding factors. In summary, our results suggest that the PUL entry item could be implemented in clinical practice to screen for respiratory impairment where spirometry is not readily available.
KW - Dysferlin
KW - Forced vital capacity
KW - Limb girdle muscular dystrophy
KW - Miyoshi myopathy
KW - Performance of upper limb (PUL)
KW - Respiratory function
UR - http://www.scopus.com/inward/record.url?scp=85201776606&partnerID=8YFLogxK
U2 - 10.1016/j.nmd.2024.08.003
DO - 10.1016/j.nmd.2024.08.003
M3 - Article
C2 - 39178649
AN - SCOPUS:85201776606
SN - 0960-8966
VL - 43
SP - 20
EP - 28
JO - Neuromuscular Disorders
JF - Neuromuscular Disorders
ER -