Table 2

Electrodiagnostic results from 20 patients with inclusion body myositis

Patient NoReferring diagnosisEMG diagnosisMNCSNCMuscleMUPs (n)Polys (%)Duration (ms) (% normal)Duration of simple MUPs (% of normal)Amplitude (μV)Spontaneous activityRecruitment
1IBMMyopathyNNTib ant201510   (68) 9.9 (67)3301+fibs4, 6
2ALSMyopathy↓a (p)NTtib ant2030 9.5 (62)  8.8 (57)4961-3+fibs/1+fascics2, 5, 6
3MNDMyopathyNNVas lat282111.3 (73)10.6 (69)3291+fibs1, 4
Biceps24010.2 (84)10.2 (84)147
Deltoid25811.9 (96)11.4 (93)215
4ALS vNMyopathyNNVas lat171217.6 (114)17.7 (115)9102+fibs/1+fascics1, 3, 4, 5
Tib ant1515 7.8 (52) 6.4 (43)641
5PMMyopathyNNBiceps2010 7.7 (60) 7.9 (62)4192+fibs4
6MyopathyMyopathyNNBiceps2010 8.4 (74) 8.5 (75)1-2+fibs/fascics/myo- kymia/CRDS5
7MyopathyMyopathyNNBiceps2050 8.4 (68) 8.4 (68)2271-2+fibs4, 6
8PMMyopathyNNBiceps2025 8.1 (65) 7.4 (60)514fibs4
9MyopathyMyopathy<a (t)NVas lat1844 9.6 (62) 9.4 (60)7491+fibs/2+fascics/C RDS1, 2, 4, 6
10SMAv myopathyMND↓a(u, p, t) ↓cv(t)↓CV(m, u, s)PLong1-2+fibs/1-2+fascics/CRDS2, 3
SMAMyopathyNot doneNot doneBiceps2124 8.4 (68) 6.7 (54)193rare fibs/CRDS2, 4
Vas lat183911.3 (72)11.6 (74)374
11MyopathyMyopathy↓a(p)NTib ant203020   (136) 8   (54)4552+fibs1, 2, 5
12MyopathyMyopathyNNVas lat282914.9 (102)13.9 (95)7291+fibs1, 2
Tib ant225012.7 (89) 9.4 (66)358
13ALSMyopathyNNBiceps206011.3 (98) 6.9 (60)5891-2+fibs/fascics/CR DS5
14ALSMNDNNPLongI1-2+fibs/1-3+fascics2, 3
15ALSSMN↓a(u, p)↓CV(m, u, s), <a(m, u)PI1-2+fibs/fascics2, 3
After bxALS v NSMN↓CV(m, p), <a(p)↓cv,a(m,u), ab (s)PI1-2+fibs/1+fascics2, 3
MyopathyMyo/SMN↓a(p, t)↓CV, a(m), ab(s)PRR,I1-2+fibs2, 4
MyopathyMyo/SMN↓CV(p, t), ↓a(p, t)↓CV, a(m, u), ab(s)
16IBM vMNDMyopathyNNNRR1+fibs2, 4
17PM vPNNon-diagNNPNNNone2
18MNDMNDNab(s)PI1-2+fibs1, 2, 4, 6
19MyopathyNormalNNNNNNone1
20MyositisNormalNAb(s)NNNNone1, 6
  • a=amplitude; ab=absent; ALS=amyotrophic lateral sclerosis; CRDS=complex repetitive discharges; fascics=fasciculations; fibs=fibrillations and positive sharp waves; CV=conduction velocity; I=increased; IBM=inclusion body myositis; m=median nerve; MND=motor neuron disease; N=normal; np=neuropathy; p=peroneal; PM=polymyositis; R=reduced; s=sural; SMA=spinal muscular atrophy; SMN=sensorimotor neuropathy; t=tibial nerve; u=ulnar nerve; 1=full recruitment on maximal effort; 2=reduced recruitment on maximal effort; 3=discrete recruitment on maximal effort; 4=full recruitment on submaximal effort; 5=full recruitment on maximal effort in a weak muscle; 6=reduced recruitment on submaximal effort.