Back to Authors

Dyck, P. James B.

https://orcid.org/0000-0003-0212-8254

Mayo Clinic

Mayo Clinic

Citations 211

Assessing Decreased Sensation and Increased Sensory Phenomena in Diabetic Polyneuropathies
Dyck, P. James B. , Herrmann, David N. , Staff, Nathan P. , Staff, Nathan P

Diabetes | October 24, 2013 | Volume: 62 | Issue: 11 | Pages: 3677-3686

10.2337/db13-0352 Get It

Loss of sensation and increased sensory phenomena are major expressions of varieties of diabetic polyneuropathies needing improved assessments for clinical and research purposes. We provide a neurobiological explanation for the apparent paradox between decreased sensation and increased sensory phenomena. Strongly endorsed is the use of the 10-g monofilaments for screening of feet to detect sensation loss, with the goal of improving diabetic management and prevention of foot ulcers and neurogenic arthropathy. We describe improved methods to assess for the kind, severity, and distribution of both large- and small-fiber sensory loss and which approaches and techniques may be useful for conducting therapeutic trials. The abnormality of attributes of nerve conduction may be used to validate the dysfunction of large sensory fibers. The abnormality of epidermal nerve fibers/1 mm may be used as a surrogate measure of small-fiber sensory loss but appear not to correlate closely with severity of pain. Increased sensory phenomena are recognized by the characteristic words patients use to describe them and by the severity and persistence of these symptoms. Tests of tactile and thermal hyperalgesia are additional markers of neural hyperactivity that are useful for diagnosis and disease management.
Approaches to Improve Epidemiological Studies of Diabetic Neuropathy: Insights from the Rochester Diabetic Neuropathy Study
Dyck, P. James B. , Melton, L. Joseph, O’Brien, Peter C. , Service, F. John

Diabetes | September 19, 2013 | Volume: 46 | Issue: Supplement_2 | Pages: S5-S8

10.2337/diab.46.2.s5 Get It

The quality of the epidemiological data on diabetic neuropathies remains poor for a variety of reasons. They include variability in 1) ascertainment of diabetes, 2 the clinical varieties of diabetic patients studied, 3) characterization of neurological dysfunction, 4) abnormal limits for neurological examinations and tests, 5) minimal criteria for neuropathy, 6) correct attribution of nondiabetic neurological disease, 7) correct attribution of type of neuropathy, 8) estimating neuropathy from use of multiple tests, and 9) estimating severity of polyneuropathy. We have tried to remedy these shortcomings in the Rochester Diabetic Neuropathy Study (RDNS). It was not possible to adequately characterize and quantitate diabetic polyneuropathies using only one or two clinical or test abnormalities. To estimate severity of diabetic polyneuropathy, the results of the neurological examination and abnormalities of nerve conduction, quantitative sensory tests, and quantitative autonomie tests were combined into a composite score. One begins by scoring a standard test of neurological deficits (impairments) of the lower limbs (NIS[LL]) and adds to this transformed numbers for percentile abnormality of seven good functional tests. This NIS(LL)+7 tests score appears to provide a much more comprehensive and stable numeric score by which to diagnose and grade severity of diabetic polyneuropathy than does the use of individual clinical or test results. This test score should be useful as a measure of change in diabetic polyneuropathy for purposes of medical practice, epidemiology studies, and controlled clinical trials. The staging approach that we introduced previously continues to provide an important measure of overall severity of diabetic polyneuropathy, taking into account both symptoms and impairments.
Clinical Reasoning: A 40-year-old man with CIDP-like illness resistant to treatment
Lahoria, Rajat , Dispenzieri, Angela , Dyck, P. James B. , Karam, Chafic , Dispenzieri, Angela

Neurology | September 2, 2013 | Volume: 81 | Issue: 10 | Pages: No page available

10.1212/wnl.0b013e3182a3523b Get It

Multicenter trial of the proficiency of smart quantitative sensation tests
Dyck, P. James B. , Argyros, Barbara, Russell, James W. , Gahnstrom, Linde E., Nalepa, Susan, Albers, James W., Lodermeier, Karen A., Zafft, Andrew J., Klein, Christopher J. , Litchy, William J. , Davies, Jenny L., Carter, Rickey E. , Melton, L. Joseph , (Appendix), members of the Cl versus NPhys Trials, Tesfaye, Solomon , (Appendix), members of the Cl versus NPhys Trials, Klein, Christopher J , Carter, Rickey E

Muscle & Nerve | August 8, 2013 | Volume: 49 | Issue: 5 | Pages: 645-653

10.1002/mus.23982 Get It

ABSTRACTIntroduction: We assessed proficiency (accuracy and intra‐ and intertest reproducibility) of smart quantitative sensation tests (smart QSTs) in subjects without and with diabetic sensorimotor polyneuropathy (DSPN). Methods: Technologists from 3 medical centers using different but identical QSTs independently assessed 6 modalities of sensation of the foot (or leg) twice in patients without (n = 6) and with (n = 6) DSPN using smart computer assisted QSTs. Results: Low rates of test abnormalities were observed in health and high rates in DSPN. Very high intraclass correlations were obtained between continuous measures of QSTs and neuropathy signs, symptoms, or nerve conductions (NCs). No significant intra‐ or intertest differences were observed. Conclusions: These results provide proof of concept that smart QSTs provide accurate assessment of sensation loss without intra‐ or intertest differences useful for multicenter trials. Smart technology makes possible efficient testing of body surface area sensation loss in symmetric length‐dependent sensorimotor polyneuropathies. Muscle Nerve 49: 645–653, 2014
Inflammatory hypertrophic cauda equina following intrathecal neural stem cell injection
Hurst, Richard W., Bosch, E. Peter, Dyck, P. James B. , Reeves, Ronald K. , Morris, Jonathan M.

Muscle & Nerve | June 6, 2013 | Volume: 48 | Issue: 5 | Pages: 831-835

10.1002/mus.23920 Get It

AN ERROR AND AN APOLOGY
Dyck, P. James. B., Dyck, P. James B.

Annals of Internal Medicine | April 12, 2013 | Volume: 66 | Issue: 5 | Pages: 1025-1025

10.7326/0003-4819-66-5-1025 Get It

Peripheral neuropathy incidence in inflammatory bowel disease
Figueroa, Juan J., Loftus, Edward V. , Harmsen, William S. , Dyck, P. James B. , Klein, Christopher J. , Klein, Christopher J , Loftus, Edward V

Neurology | April 10, 2013 | Volume: 80 | Issue: 18 | Pages: 1693-1697

10.1212/wnl.0b013e3182904d16 Get It

DNMT1 mutation hot spot causes varied phenotypes of HSAN1 with dementia and hearing loss
Klein, Christopher J. , Bird, T., Ertekin‐Taner, Nilüfer , Lincoln, Sarah, Hjorth, Robert, Kwok, John B. , Mer, Georges , Dyck, P. James B. , Nicholson, Garth A. , Wu, Yanhong , Klein, Christopher J , Kwok, John B J

Neurology | January 31, 2013 | Volume: 80 | Issue: 9 | Pages: 824-828

10.1212/wnl.0b013e318284076d Get It

A trial of proficiency of nerve conduction: Greater standardization still needed
Dyck, P. James B. , Albers, James W., Wolfe, James, Bolton, Charles F., WALSH, NANCY, Klein, Christopher J. , Zafft, Andrew J., Russell, James W. , Thomas, Karen, Davies, Jenny L., Carter, Rickey E. , Melton, L. Joseph , Litchy, William J. , Klein, Christopher J , Carter, Rickey E

Muscle & Nerve | December 27, 2012 | Volume: 48 | Issue: 3 | Pages: 369-374

10.1002/mus.23765 Get It

ABSTRACTIntroductionThe aim of this study was to test the proficiency (accuracy among evaluators) of measured attributes of nerve conduction (NC).MethodsExpert clinical neurophysiologists, without instruction or consensus development, from 4 different medical centers, independently assessed 8 attributes of NC in 24 patients with diabetes mellitus (DM) on consecutive days.ResultsNo significant intraobserver differences between days 1 and 2 were found, but significant interobserver differences were seen. Use of standard reference values did not correct for these observed differences.ConclusionsInterobserver variability was attributed to differences in performance of NC. It was of sufficient magnitude that it is of concern for the conduct of therapeutic trials. To deal with interrater variability in therapeutic trials, the same electromyographers should perform all NC assessments of individual patients or, preferably, NC procedures should be more standardized. A further trial is needed to test whether such standardization would eliminate interobserver variability. Muscle Nerve 48: 369–374, 2013