Values and diagnostic accuracy of sensory nerve action potentials in control participants and participants with diabetes with and without clinical diabetic neuropathy, based on neuropathy scale measurements
Background The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy‐assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature. Methods The Utah Ea...
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Published in: | Brain and behavior Vol. 14; no. 2; pp. e3423 - n/a |
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Abstract | Background
The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy‐assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature.
Methods
The Utah Early Neuropathy Scale (UENS), Michigan neuropathy‐screening instrument, and nerve conduction data were collected prospectively. We described and compared the values of the sural, superficial peroneal sensory (SPS), and superficial radial SNAP amplitude in different age groups for three groups. Group 1 (G1)—control participants (UENS <5), group 2 (G2)—participants with diabetes without clinical diabetic neuropathy (UENS <5), and group 3 (G3)—participants with clinical diabetic neuropathy (UENS ≥5). We also described the diagnostic accuracy of single‐nerve amplitude and a combined sensory polyneuropathy index (CSPNI) that consists of four total points (one point for each of the following nerves if their amplitude was <25% lower limit of normal: right sural, left sural, right SPS, and left SPS potentials).
Results
We assessed 135 participants, including 41, 37, and 57 participants in G1, G2, and G3, respectively, with age median (interquartile ranges) of 51 (45–56), 47 (38–56), and 54 (51–61) years, respectively, whereas 19 (46.3%), 18 (48.7%), and 32 (56.14%) of them were males, respectively. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) scores were 68.4%, 92.3%, 86.7%, and 80% for the sural amplitude; 86%, 58.3%, 62%, and 84% for the SPS amplitude; 66.7%, 94.4%, 90.5%, and 78.2% for the CSPNI of 3; and 54.4%, 98.6%, 96.9%, and 73.2% for the CSPNI of 4, respectively.
Conclusion
Sural nerve had a high specificity for neuropathy; however, the CSPNI had the highest specificity and PPV, whereas the SPS had the highest sensitivity and NPV.
We described the sensitivity, specificity, positive predictive value, and negative predictive values of sensory nerve action potentials. We used a validated neuropathy scales to classify our participants into neuropathy and no neuropathy groups. These diagnostic accuracies were not reported in the previous literature. |
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AbstractList | Background
The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy‐assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature.
Methods
The Utah Early Neuropathy Scale (UENS), Michigan neuropathy‐screening instrument, and nerve conduction data were collected prospectively. We described and compared the values of the sural, superficial peroneal sensory (SPS), and superficial radial SNAP amplitude in different age groups for three groups. Group 1 (G1)—control participants (UENS <5), group 2 (G2)—participants with diabetes without clinical diabetic neuropathy (UENS <5), and group 3 (G3)—participants with clinical diabetic neuropathy (UENS ≥5). We also described the diagnostic accuracy of single‐nerve amplitude and a combined sensory polyneuropathy index (CSPNI) that consists of four total points (one point for each of the following nerves if their amplitude was <25% lower limit of normal: right sural, left sural, right SPS, and left SPS potentials).
Results
We assessed 135 participants, including 41, 37, and 57 participants in G1, G2, and G3, respectively, with age median (interquartile ranges) of 51 (45–56), 47 (38–56), and 54 (51–61) years, respectively, whereas 19 (46.3%), 18 (48.7%), and 32 (56.14%) of them were males, respectively. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) scores were 68.4%, 92.3%, 86.7%, and 80% for the sural amplitude; 86%, 58.3%, 62%, and 84% for the SPS amplitude; 66.7%, 94.4%, 90.5%, and 78.2% for the CSPNI of 3; and 54.4%, 98.6%, 96.9%, and 73.2% for the CSPNI of 4, respectively.
Conclusion
Sural nerve had a high specificity for neuropathy; however, the CSPNI had the highest specificity and PPV, whereas the SPS had the highest sensitivity and NPV.
We described the sensitivity, specificity, positive predictive value, and negative predictive values of sensory nerve action potentials. We used a validated neuropathy scales to classify our participants into neuropathy and no neuropathy groups. These diagnostic accuracies were not reported in the previous literature. We described the sensitivity, specificity, positive predictive value, and negative predictive values of sensory nerve action potentials. We used a validated neuropathy scales to classify our participants into neuropathy and no neuropathy groups. These diagnostic accuracies were not reported in the previous literature. Abstract Background The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy‐assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature. Methods The Utah Early Neuropathy Scale (UENS), Michigan neuropathy‐screening instrument, and nerve conduction data were collected prospectively. We described and compared the values of the sural, superficial peroneal sensory (SPS), and superficial radial SNAP amplitude in different age groups for three groups. Group 1 (G1)—control participants (UENS <5), group 2 (G2)—participants with diabetes without clinical diabetic neuropathy (UENS <5), and group 3 (G3)—participants with clinical diabetic neuropathy (UENS ≥5). We also described the diagnostic accuracy of single‐nerve amplitude and a combined sensory polyneuropathy index (CSPNI) that consists of four total points (one point for each of the following nerves if their amplitude was <25% lower limit of normal: right sural, left sural, right SPS, and left SPS potentials). Results We assessed 135 participants, including 41, 37, and 57 participants in G1, G2, and G3, respectively, with age median (interquartile ranges) of 51 (45–56), 47 (38–56), and 54 (51–61) years, respectively, whereas 19 (46.3%), 18 (48.7%), and 32 (56.14%) of them were males, respectively. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) scores were 68.4%, 92.3%, 86.7%, and 80% for the sural amplitude; 86%, 58.3%, 62%, and 84% for the SPS amplitude; 66.7%, 94.4%, 90.5%, and 78.2% for the CSPNI of 3; and 54.4%, 98.6%, 96.9%, and 73.2% for the CSPNI of 4, respectively. Conclusion Sural nerve had a high specificity for neuropathy; however, the CSPNI had the highest specificity and PPV, whereas the SPS had the highest sensitivity and NPV. BACKGROUNDThe assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy-assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature.METHODSThe Utah Early Neuropathy Scale (UENS), Michigan neuropathy-screening instrument, and nerve conduction data were collected prospectively. We described and compared the values of the sural, superficial peroneal sensory (SPS), and superficial radial SNAP amplitude in different age groups for three groups. Group 1 (G1)-control participants (UENS <5), group 2 (G2)-participants with diabetes without clinical diabetic neuropathy (UENS <5), and group 3 (G3)-participants with clinical diabetic neuropathy (UENS ≥5). We also described the diagnostic accuracy of single-nerve amplitude and a combined sensory polyneuropathy index (CSPNI) that consists of four total points (one point for each of the following nerves if their amplitude was <25% lower limit of normal: right sural, left sural, right SPS, and left SPS potentials).RESULTSWe assessed 135 participants, including 41, 37, and 57 participants in G1, G2, and G3, respectively, with age median (interquartile ranges) of 51 (45-56), 47 (38-56), and 54 (51-61) years, respectively, whereas 19 (46.3%), 18 (48.7%), and 32 (56.14%) of them were males, respectively. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) scores were 68.4%, 92.3%, 86.7%, and 80% for the sural amplitude; 86%, 58.3%, 62%, and 84% for the SPS amplitude; 66.7%, 94.4%, 90.5%, and 78.2% for the CSPNI of 3; and 54.4%, 98.6%, 96.9%, and 73.2% for the CSPNI of 4, respectively.CONCLUSIONSural nerve had a high specificity for neuropathy; however, the CSPNI had the highest specificity and PPV, whereas the SPS had the highest sensitivity and NPV. The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy-assessment tools to classify participants into groups with and without neuropathy was not previously described in the literature. The Utah Early Neuropathy Scale (UENS), Michigan neuropathy-screening instrument, and nerve conduction data were collected prospectively. We described and compared the values of the sural, superficial peroneal sensory (SPS), and superficial radial SNAP amplitude in different age groups for three groups. Group 1 (G1)-control participants (UENS <5), group 2 (G2)-participants with diabetes without clinical diabetic neuropathy (UENS <5), and group 3 (G3)-participants with clinical diabetic neuropathy (UENS ≥5). We also described the diagnostic accuracy of single-nerve amplitude and a combined sensory polyneuropathy index (CSPNI) that consists of four total points (one point for each of the following nerves if their amplitude was <25% lower limit of normal: right sural, left sural, right SPS, and left SPS potentials). We assessed 135 participants, including 41, 37, and 57 participants in G1, G2, and G3, respectively, with age median (interquartile ranges) of 51 (45-56), 47 (38-56), and 54 (51-61) years, respectively, whereas 19 (46.3%), 18 (48.7%), and 32 (56.14%) of them were males, respectively. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) scores were 68.4%, 92.3%, 86.7%, and 80% for the sural amplitude; 86%, 58.3%, 62%, and 84% for the SPS amplitude; 66.7%, 94.4%, 90.5%, and 78.2% for the CSPNI of 3; and 54.4%, 98.6%, 96.9%, and 73.2% for the CSPNI of 4, respectively. Sural nerve had a high specificity for neuropathy; however, the CSPNI had the highest specificity and PPV, whereas the SPS had the highest sensitivity and NPV. |
Author | Alamri, Bashayr Alshora, Weam Alkully, Hussien S. Bamaga, Ahmed K. Alrawaili, Moafaq S. Alshareef, Aysha A. Milyani, Haneen Abuzinadah, Ahmad R. |
AuthorAffiliation | 4 Neurophysiology Department, National Neuroscience Institute King Fahad Medical City Riyadh Saudi Arabia 8 Division of Pediatric Neurology, Department of Pediatrics King Faisal Specialist Hospital and Research Centre Jeddah Saudi Arabia 1 Department of Neurology, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia 7 Pediatric Neurology Unit, Department of Pediatric, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia 6 Department of Family Medicine King Abdulaziz University Hospital, King Abdulaziz University Jeddah Saudi Arabia 3 Neurology Section, Department of Neurosciences King Faisal Specialist Hospital and Research Centre Jeddah Saudi Arabia 5 Internal Medicine Department, Neurology division King Fahad General Hospital Jeddah Saudi Arabia 2 Neuromuscular Medicine Unit King Abdulaziz University Hospital, King Abdulaziz University Jeddah Saudi Arabia |
AuthorAffiliation_xml | – name: 3 Neurology Section, Department of Neurosciences King Faisal Specialist Hospital and Research Centre Jeddah Saudi Arabia – name: 8 Division of Pediatric Neurology, Department of Pediatrics King Faisal Specialist Hospital and Research Centre Jeddah Saudi Arabia – name: 7 Pediatric Neurology Unit, Department of Pediatric, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia – name: 2 Neuromuscular Medicine Unit King Abdulaziz University Hospital, King Abdulaziz University Jeddah Saudi Arabia – name: 4 Neurophysiology Department, National Neuroscience Institute King Fahad Medical City Riyadh Saudi Arabia – name: 1 Department of Neurology, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia – name: 5 Internal Medicine Department, Neurology division King Fahad General Hospital Jeddah Saudi Arabia – name: 6 Department of Family Medicine King Abdulaziz University Hospital, King Abdulaziz University Jeddah Saudi Arabia |
Author_xml | – sequence: 1 givenname: Ahmad R. orcidid: 0000-0001-5442-6734 surname: Abuzinadah fullname: Abuzinadah, Ahmad R. email: aabuzinadah@kau.edu.sa organization: King Abdulaziz University Hospital, King Abdulaziz University – sequence: 2 givenname: Moafaq S. surname: Alrawaili fullname: Alrawaili, Moafaq S. organization: King Abdulaziz University Hospital, King Abdulaziz University – sequence: 3 givenname: Aysha A. surname: Alshareef fullname: Alshareef, Aysha A. organization: King Abdulaziz University Hospital, King Abdulaziz University – sequence: 4 givenname: Hussien S. surname: Alkully fullname: Alkully, Hussien S. organization: King Faisal Specialist Hospital and Research Centre – sequence: 5 givenname: Haneen surname: Milyani fullname: Milyani, Haneen organization: King Fahad Medical City – sequence: 6 givenname: Bashayr surname: Alamri fullname: Alamri, Bashayr organization: King Fahad General Hospital – sequence: 7 givenname: Weam surname: Alshora fullname: Alshora, Weam organization: King Abdulaziz University Hospital, King Abdulaziz University – sequence: 8 givenname: Ahmed K. surname: Bamaga fullname: Bamaga, Ahmed K. organization: King Faisal Specialist Hospital and Research Centre |
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Snippet | Background
The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated... The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated neuropathy-assessment tools to... We described the sensitivity, specificity, positive predictive value, and negative predictive values of sensory nerve action potentials. We used a validated... BackgroundThe assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated... BACKGROUNDThe assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated... Abstract Background The assessment of the normative values of sensory nerve action potentials (SNAP) and their diagnostic accuracies using validated... |
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SubjectTerms | Accuracy Data collection Diabetes Diabetic neuropathy diagnosis neuropathy Original Patients Peripheral neuropathy screening sensitivity Sensitivity analysis |
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Title | Values and diagnostic accuracy of sensory nerve action potentials in control participants and participants with diabetes with and without clinical diabetic neuropathy, based on neuropathy scale measurements |
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