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. Author manuscript; available in PMC: 2023 Aug 8.
Published in final edited form as: J Neuromuscul Dis. 2023;10(3):301–314. doi: 10.3233/JND-230001

Table 2.

Analysis of published evidence on MFM’s measurement properties depending on the diagnosis

All NMD DMD DM1 SMA FSHD CMT CMD, CM
Structural validity + Moderate ? Moderate + High ? No evidence + High Ceiling effect especially for D2 and D3 + High + Moderate
Internal consistency + High ? Moderate ? No evidence + High ? No evidence ? No evidence + High
Reliability + High ? Low ? No evidence + High ? No evidence ? No evidence Inter-rater: + Intra-rater: ? Moderate
Cross-cultural validity Low ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence
Criterion validity ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence
Convergent validity + High ? No evidence ? No evidence + High + Moderate ? No evidence + High
Discriminant validity + High ? No evidence ? No evidence + High ? No evidence ? No evidence + High Floor and ceiling effect
Responsiveness + High + High ? No evidence + High Low CMT1: −
CMT2:+
High
+ Moderate
Measurement error ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence ? No evidence

GRADE level of evidence: green: high, orange: moderate, red: low, grey: no evidence. Rating of measurement properties: +: sufficient, ?: indeterminate, –: low. NMD: neuromuscular disease, CMD: congenital muscular dystrophy, CM: congenital myopathy, DM1: myotonic dystrophy type 1, SMA: spinal muscular atrophy, FSHD: facio-scapulo-humeral dystrophy, CMT: Charcot-Marie-Tooth disease, DMD: Duchenne muscular dystrophy.