Electrodiagnostic Parameters in Patients With Impaired Glucose Tolerance and Diabetes Mellitus

NCT ID: NCT01094418

Last Updated: 2010-03-29

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 150 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2009-06-30
• Study Completion Date: 2010-02-28

Brief Summary

The purpose of this study is to evaluate the distal sensory nerves of the feet, namely, the dorsal sural, medial dorsal cutaneous and medial plantar nerves, in patients with impaired glucose tolerance and diabetes mellitus type 2 and compare these parameters to those from healthy participants.

Detailed Description

Diabetic Peripheral polyneuropathy (DPP) presents as a slowly progressive primary sensory deficit in length dependent fashion, to result in the classic stocking glove distribution. There is recent evidence to indicate that patients with impaired glucose tolerance ( IGT) on OGTT, the prediabetic stage, have three times the prevalence of distal peripheral polyneuropathy than age matched controls. Patients with IGT, even in their preclinical stages, though they have less severe neuropathy than those with diabetes mellitus, have predominant sensory fiber involvement. To support this, other studies of skin biopsies of IGT patients have shown that microvascular abnormalities and neuropathic changes can occur in the prediabetic stage.

Because DPP is length dependent, it is necessary to evaluate the distal sensory nerves, other than the standard sural and superficial peroneal nerves. To support this theory, recent electrodiagnostic studies in DM patients have shown that albeit normal conduction parameters in the above mentioned two nerves, abnormal parameters can be detected in the more distal sensory nerves, such as the dorsal sural nerve, medial plantar nerves and medial dorsal cutaneous nerve.

Although the importance of evaluating the distal sensory nerves has gained much attention, no study has addressed the issue whether NCS parameters of these distal sensory nerves in IGT patients are significantly different from those of healthy controls with no medical condition, and whether these parameters are different to those with patients with diabetes mellitus, who have no previous history of peripheral polyneuropathy.

With this objective in mind, NCS of the distal sensory nerves of the feet were performed to three groups; normal healthy control group, IGT group and diabetes mellitus group.

Conditions

Impaired Glucose Tolerance; Peripheral Polyneuropathy; DM

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

IGT group

IGT diagnosed by endocrinologist

Nerve conduction studies ( NCS) of the peripheral nerves

Intervention Type: OTHER

Standard NCS of the sural, superficial peroneal sensory nerves, peroneal, tibial motor nerves, radial and median sensory nerves, median motor nerves, F-wave studies of the Tibial and median nerves.

NCS of the distal sensory nerves; dorsal sural Medial dorsal cutaneous and medial plantar nerves.

DM group

DM diagnosed by endocrinologist and whose primary NCS screening shows SNAP amplitudes of sural and superficial peroneal nerves greater than 10mA DM patients with no previous diagnosis of peripheral polyneuropathy

Nerve conduction studies ( NCS) of the peripheral nerves

Intervention Type: OTHER

Standard NCS of the sural, superficial peroneal sensory nerves, peroneal, tibial motor nerves, radial and median sensory nerves, median motor nerves, F-wave studies of the Tibial and median nerves.

NCS of the distal sensory nerves; dorsal sural Medial dorsal cutaneous and medial plantar nerves.

Normal healthy participants

Normal health participants with no previous history of DM, IGT, thyroid disorder, hypercholesterolemia, or other condition associated with peripheral polyneuropathy

Nerve conduction studies ( NCS) of the peripheral nerves

Intervention Type: OTHER

Standard NCS of the sural, superficial peroneal sensory nerves, peroneal, tibial motor nerves, radial and median sensory nerves, median motor nerves, F-wave studies of the Tibial and median nerves.

NCS of the distal sensory nerves; dorsal sural Medial dorsal cutaneous and medial plantar nerves.

Interventions

Nerve conduction studies ( NCS) of the peripheral nerves

Standard NCS of the sural, superficial peroneal sensory nerves, peroneal, tibial motor nerves, radial and median sensory nerves, median motor nerves, F-wave studies of the Tibial and median nerves.

NCS of the distal sensory nerves; dorsal sural Medial dorsal cutaneous and medial plantar nerves.

Intervention Type: OTHER

Other Intervention Names

EMG(Viking )

Eligibility Criteria

Inclusion Criteria

• For the normal healthy control group
• Healthy participants with normal NCS parameters
• For the IGT group
• Men or women aged 20-70 with IGT referred by the department of endocrinology, with FBS 100-126 mg/dl, post 2 hour OTT - 140-200mg/dl,lasting more than one year.
• Patients willing to undergo NCS.
• For the DM group
• Men or women aged 20-70 with DM type II patients referred by the department of endocrinology, with no previous diagnosis of peripheral polyneuropathy and who showed SNAP amplitudes of the sural and superficial peroneal nerves above 10mA.
• Patients willing to undergo NCS.

Exclusion Criteria

• No previous diagnosis of any systemic condition related to peripheral polyneuropathy (malnutrition, alcoholic hepatitis, diabetes mellitus( normal group)), no previous medication history, such as chemotherapeutics
• No symptom or sign of peripheral polyneuropathy, no history of tingling sensation, muscle weakness, or gait disturbance
• Skin lesion or swelling that would interfere with NCS conduction
• Previous diagnosis or clinical symptoms that would indicate the presence of mononeuropathy or entrapment neuropathy of the lower extremity.
• Previous trauma episode of the lower extremity
• History of alcohol ( exceeding alcohol consumption of 170g per week ) or substance abuse,
• Pregnancy
• DM group
• Presence of undiagnosed peripheral polyneuropathy determined by screening of the sural and superficial peroneal nerves.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

The Catholic University of Korea

OTHER

Sponsor Role: lead

Responsible Party

Dept. of Rehabilitation Medicine,Bucheon St. Mary's Hospital,College of Medicine,The Catholic University of Korea

Principal Investigators

Geun Young Park, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

College of Medicine, Catholic University of Korea

Locations

Catholic University of Medicine, College of Medicine, Bucheon St. Mary's Hospital, Department of Rehabilitation Medicine

Bucheon-si, Kyoungido, South Korea

Countries

South Korea

Other Identifiers

5-2008-B0001-00099

Identifier Type: -

Identifier Source: org_study_id