Dissociated atrophy of intrinsic hand muscles, termed the split hand, appears to be a specific feature of amyotrophic lateral sclerosis (ALS). Consequently, a novel neurodiagnostic test, termed the split hand index, was developed to quantify the clinical phenomenon of the split hand, which differentiated ALS from mimic disorders.
The split hand phenomenon refers to predominant wasting of thenar muscles and is an early and specific feature of amyotrophic lateral sclerosis (ALS). A novel split hand index (SI) was developed to quantify the split hand phenomenon, and its diagnostic utility was assessed in ALS patients. The split hand index was derived by dividing the product of the compound muscle action potential (CMAP) amplitude recorded over the abductor pollicis brevis and first dorsal interosseous muscles by the CMAP amplitude recorded over the abductor digiti minimi muscle. In order to assess the diagnostic utility of the split hand index, ALS patients were prospectively assessed and their results were compared to neuromuscular disorder patients. The split hand index was significantly reduced in ALS when compared to neuromuscular disorder patients (P<0.0001). Limb-onset ALS patients exhibited the greatest reduction in the split hand index, and a value of 5.2 or less reliably differentiated ALS from other neuromuscular disorders. Consequently, the split hand index appears to be a novel diagnostic biomarker for ALS, perhaps facilitating an earlier diagnosis.
The split hand, refers to preferential atrophy of the thenar complex group of intrinsic hand muscles [abductor pollicis brevis (APB) and first dorsal interosseous (FDI)], with relative preservation of hypothenar muscles, and is a specific and early clinical feature of amyotrophic lateral sclerosis (ALS)1-4. The finding that the split hand sign is specific for ALS, suggests a potential role for the split hand sign as a diagnostic biomarker in ALS3.
Quantification of the split hand sign, through the development of a novel neurophysiological biomarker, may further aid in ALS diagnosis. Specifically, the split hand index (SI), which quantifies the split hand phenomenon, is derived by multiplying the compound muscle action potential (CMAP) amplitude recorded over the thenar complex muscles (APB and FDI), and dividing this product by the CMAP amplitude recorded over the hypothenar muscles (namely the abductor digiti minimi, ADM)5.
The diagnosis of ALS relies largely on clinically based criteria encompassing a combination of upper and lower motor neuron signs6. These criteria, however, were deemed insensitive especially in establishing a diagnosis of ALS in the early stages of the disease process7-10. A recent modification of the diagnostic criteria were developed11, and although these criteria appear to increase the diagnostic sensitivity12-16, the increase sensitivity seems restricted to bulbar-onset ALS patients15.
In the absence of a pathognomonic test, the diagnosis of ALS may be significantly delayed8. Ultimately, the institution of neuroprotective therapies and recruitment into clinical trials may be delayed, perhaps beyond the critical therapeutic window period9,17. Consequently, the diagnostic utility of the SI was prospectively assessed in sporadic ALS patients.
1. Patient Preparation
2. Clinical Assessment
3. Neurophysiological Assessment
4. Analysis and Interpretation
Clinical Phenotype
In total, 44 ALS patients were studied, of which 76% (N=33) were classified as definite or probable and 24% (N=11) as possible ALS according to the Awaji criteria11. The diagnosis of ALS was confirmed in the “possible” cohort after extensive investigations and clinical follow-up for up to 3 years and 53% died during this period. Bulbar-onset disease was evident in 41%, while limb-onset in 59% of ALS patients. At the time of assessment, mean disease duration was 18.9±3.1 months, with a median ALSFRS-R score being 41(32-45), indicating a moderate degree of disability.
The neuromuscular control group comprised 121 patients (mean age 54 years) and included the following diagnosis: entrapment neuropathies-carpal tunnel syndrome (CTS) and ulnar neuropathy at the elbow (UNE), N=62; demyelinating neuropathy (N=9); axonal sensorimotor polyneuropathy (N=36); cervical radiculopathy (11); spino-bulbar muscular atrophy (N=1); Hirayama’s disease (N=1); spinal muscular atrophy (N=1).
Neurophysiological Studies
In ALS patients, there was a significant reduction of CMAP amplitude recorded over the APB (ALS, 3.9±0.5 mV; neuromuscular disorders 8.1± 0.2 mV, P<0.001), FDI (ALS, 4.8±0.7 mV; neuromuscular disorders 10.7±0.3 mV, P<0.001) and ADM (ALS, 6.1±0.5 mV; neuromuscular disorders 9.7±0.2 mV, P<0.001). Importantly, the reduction in CMAP amplitudes was more prominent when recording over the APB (CMAPAPB 3.9±0.5 mV; CMAPADM 6.1±0.5 mV P<0.001) and FDI (CMAPFDI 4.8±0.7 mV; CMAPADM 6.1±0.5 mV P<0.05) muscles then ADM in the ALS cohort.
Of further relevance, the extent of CMAP reduction was more prominent in limb-onset patients when recording over APB (CMAPLIMB-ONSET 3.8±0.4 mV; CMAPBULBAR-ONSET 5.3±0.6 mV P<0.05), FDI (CMAPLIMB-ONSET 4.4±0.7 mV; CMAPBULBAR-ONSET 7.0±0.9 mV P<0.05) and ADM (CMAPLIMB-ONSET 5.8±0.5 mV; CMAPBULBAR-ONSET 7.6±0.6 mV P<0.01) muscles compared to bulbar onset ALS patients. In contrast, the reduction in CMAP amplitudes was most prominent when recording over the APB (8.1±0.2 mV, P<0.0001) and ADM (9.7±0.2 mV, P<0.01) muscles in the neuromuscular cohort (CMAPFDI 10.7±0.3 mV).
Combining the CMAP amplitudes, it was evident that there was a significant reduction of the split hand index in ALS patients compared to neuromuscular disorder patients (ALS 3.5±0.6; neuromuscular disorders 9.1±0.3, P<0.0001, Figure 2A)21. While this reduction in the split hand index was a ubiquitous finding in ALS, it was most pronounced in ALS patients with limb-onset disease (SILIMB-ONSET2.3±0.5; SIBULBAR-ONSET 5.3±1.2, P<0.0001, Figure 2B)21.
Analysis of receiver operating characteristic curves disclosed a good diagnostic accuracy of the split hand index in differentiating ALS from other neuromuscular disorders, as indicated by the fact that the area under curve (AUC) was 0.83 (P<0.0001, Figure 3A)21. An SI value of 5.2 or less, as indicated by dotted black lines (Figure 3A), differentiated ALS from other neuromuscular disorders21. Importantly, the diagnostic utility of the split hand index was greater in ALS patients with limb-onset disease (Figure 3B)21.
In order to assess the diagnostic utility of the split hand index, SI values were compared between those ALS patients meeting the “definite” versus “possible” diagnostic category on the Awaji-Shima criteria11. Importantly, there was a significant reduction of SI in patients classified as “possible” ALS (ALS POSSIBLE SI 5.1±0.8; neuromuscular disorders 9.1±0.3, P<0.01). In addition, of the 11 patients classified as possible ALS, 64% exhibited a reduction in the split hand index value of less than 5.2. Taken together, these findings suggest that an abnormal split hand index may support a diagnosis of ALS in up to 64% of patients not meeting the “definite/probable” Awaji diagnostic criteria.
Of potential prognostic relevance, the split hand index significantly correlated with the total MRC score (rho = 0.7, P<0.001) and MRC score from the thenar eminence (rho = 0.8, P<0.001). Of further relevance, the SI exhibited a significant correlation with the rate of disease progression (rho = – 0.4, P<0.05). These findings indicate that SI is associated with disease severity and progression, thereby suggesting a potential role for the SI in ALS prognostication.
Figure 1. Split hand sign refers to preferential wasting of the thenar complex group of muscles [abductor pollicis brevis (APB) and first dorsal interosseous (FDI)] muscles when compared to the hypothenar [abductor digit minimi (ADM)] muscles. The split hand index is calculated by multiplying the compound muscle action potential (CMAP) amplitude recorded over the APB by that recorded over the FDI and dividing the product by the CMAP amplitude recorded over the ADM. (In part reproduced from Menon and colleagues. Split hand index for the diagnosis of amyotrophic lateral sclerosis. From Menon et al.21
Figure 2. (A) The split hand index (SI) was significantly reduced in amyotrophic lateral sclerosis (ALS) when compared to neuromuscular disorder patients (NMS). (B) The reduction in SI was most prominent in ALS in patients with limb-onset disease. ***P<0.001; ****P<0.0001.
Figure 3. (A) The split hand index (SI) robustly differentiated amyotrophic lateral sclerosis (ALS) from neuromuscular disorder patients (NMS), with an optimal diagnostic cut-off value being 5.2. (B) The diagnostic utility of SI was more prominent in limb-onset ALS patients. (In part reproduced from Menon and colleagues. Split hand index for the diagnosis of amyotrophic lateral sclerosis. From Menon et al.21
The present study reports on the diagnostic utility of the split hand index in ALS, a novel neurophysiological diagnostic biomarker. The SI reliably distinguished ALS from neuromuscular disorders, with an optimal diagnostic cut-off value of 5.2. The reduction in the SI was most prominent in limb-onset ALS patients. Importantly, a substantial proportion of ALS patients that were classified in the diagnostic “possible” category as per the recently developed diagnostic criteria11, exhibited an abnormal SI. Taken together, findings from the present study suggest that the split hand index may be a diagnostic biomarker of ALS, potentially aiding in an earlier diagnosis of ALS.
Diagnostic criteria, relying on the presence of upper and lower motor neuron dysfunction in multiple regions, have been developed to aid the diagnosis of ALS6,11,22. These criteria, however, have been shown as insensitive and at times limited by patient tolerability due to the need to perform extensive needle EMG sampling7-10,14-16. Consequently, critical diagnostic delay may ensue, perhaps beyond the therapeutic window period.
The split hand index, a simple neurophysiological biomarker, can be readily performed in a clinical setting. Importantly, the present study underscores the diagnostic utility of the split hand index in ALS, particularly in limb-onset disease. Of relevance, the finding that reduction in the split hand index was an early feature in ALS, further underscores its diagnostic utility. Ultimately, the application of SI may lead to recruitment of ALS patients into clinical trials at an earlier stage in the disease process where effectiveness of future neuroprotective agents may be at their peak.
A potential limitation of the split hand index may occur in the setting of coexistent focal pressure mononeuropathies, particularly carpal tunnel syndrome and ulnar neuropathy at the elbow. Clinical, neurophysiological, and radiological correlation should then be utilized to assess for a specific pattern of pathology and alternative techniques need to be implemented so as to establish a diagnosis of ALS23,24. In addition, the SI may be limited in advanced disease, when there may be global atrophy of intrinsic hand muscles. As with focal mononeuropathies, other diagnostic modalities should be utilized to confirm the diagnosis of ALS. In addition, avoiding a contribution from a volume conducted response to the CMAP amplitude is critical prior to conclude the diagnostic value of the SI. Volume conduction may be reduced by appropriate positioning of recording electrodes so as to ensure a CMAP response with negative take-off and appropriate stimulation intensities should be utilized to prevent cross stimulation. If all such potential limitations are addressed, the SI could be utilized as a potential diagnostic aid in ALS.
The authors have nothing to disclose.
Funding support from the Motor Neuron Disease Research Institute of Australia (MNDRIA), Sylvia and Charles Viertel Charitable Foundation Clinical Investigator grant, Ramaciotti Foundation and National Health and Medical Research Council of Australia (Project grant number APP1024915) is gratefully acknowledged.
Abrasive gel (Nu Prep) | Weaver and Company | N-TA/PH-3 ENG | Skin preperation |
(www.doweaver.com) | |||
Alcohol wipe | Triad Disposables | 103101 | Skin preperation |
(www.triad-group.net) | |||
Recording gel (Ten20 Conductive gel) | Weaver and Company | N-TA/PH-3 ENG | Recording motor responses |
(www.doweaver.com) | |||
Amyotrophic lateral sclerosis rating scale-revised questionnaire | Publication | Experimental builder | Stage disease |
(see Methods and References) | |||
Medical Research Council muscle strength scale | Medical Research Council-UK | Experimental builder | Stage disease |
(see Methods and References) | |||
Table of equipment used | |||
Name of the equipment used | Company | Catalog number | Comments |
Nerve conduction machine (Synergy/Nicolet EDX) | CareFusion (www.carefusion.com/medical-products/neurology) | SA110106M | To measure split hand index |
Synergy software | CareFusion | 765654679 | To measure split hand index |
(www.carefusion.com/medical-products/neurology) | |||
Tem millimeter gold cup disc electrodes | Grass Technologies | F-E5GH-60 | To record motor responses |
(www.grasstechnologies.com) | |||
Neural earth plate | Westmead Hospital | Experimental builder | To record limb temperature |
Thermometer | Westmead Hospital | Experimental builder | To record limb temperature |