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Letters: Comments and Responses

4-g Monofilament Is Clinically Useful for Detecting Diabetic Peripheral Neuropathy

  1. Yukihiro Nagai, MD, PHD,
  2. Yu Sugiyama, MD, PHD,
  3. Toshio Abe, MD, PHD and
  4. Gakuji Nomura, MD, PHD
  1. From the Departments of Internal Medicine (Y.N., T.A., G.N.) and Neurology (Y.S.), Kanazawa Municipal Hospital, Kanazawa, Ishikawa, Japan.
  1. Address correspondence to Yukihiro Nagai, MD, the Department of Internal Medicine, Kanazawa Municipal Hospital, 3-7-3 Heiwa-machi, Kanazawa, Ishikawa, Japan 921-8105. E-mail: ynagai{at}p2223.nsk.ne.jp .
Diabetes Care 2001 Jan; 24(1): 183-184. https://doi.org/10.2337/diacare.24.1.183
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The American Diabetes Association recommends the use of the 10-g Semmes-Weinstein monofilament for the early identification of diabetic patients at risk for foot ulceration (1). However, this 10-g monofilament can only detect advanced diabetic peripheral neuropathy (DPN). Thus, we evaluated whether other monofilaments could be useful for the detection of early DPN with high sensitivity and high specificity, and compared the results of monofilament tests with the results of microneurography.

We recruited 65 patients (aged 61.0 ± 1.3 years, diabetes duration 9.8 ± 1.0 years [range 1-35]) with type 2 diabetes to participate in this study. Of these patients, 24 were treated with oral hypoglycemic agents, 32 were treated with insulin, and 9 were kept on a controlled diet only. In addition, 19 patients had background retinopathy, 2 had proliferative retinopathy, and 21 had microalbuminuria (>30 mg/day) defined as diabetic nephropathy. Patients with at least two of the following criteria were diagnosed with DNP: 1) numbness in the toes, 2) loss of ankle jerk, and 3) decreased vibratory sensation assessed by a 128-Hz tuning fork (<10 s). Participants were tested for their ability to sense three kinds of Semmes-Weinstein monofilament, with target forces of 2, 4, and 10 g, respectively, at three sites of the foot: the great toe, the plantar aspect of the first metatarsal, and the plantar aspect of the fifth metatarsal (2,3). Individual cut off monofilament was defined as the lowest target force to sense. Microneurography was performed as previously described (4).

The sensitivity and specificity of the 2-g monofilament in the detection of DPN were 0.48 and 0.86, respectively. On the other hand, the corresponding values for the 4-g monofilament, 0.85 and 0.73, respectively, were quite close to those for the 10-g monofilament (0.88 and 0.68, respectively). Thus, we concluded that the 4-g monofilament was clinically useful for detecting DPN. Participants were divided into two groups based on a cut off target force: the 2-g monofilament group (group A, n = 52) and the 4- and 10-g monofilaments group (group B, n = 13). The maximal nerve velocity of group B was significantly lower than that of group A (50.4 ± 1.5 vs. 57.3 ± 0.6 m/s, P < 0.0001). The amplitude of group B was also significantly lower than that of group A (119.9 ± 31.8 vs. 184.1 ± 11.5 μV, P < 0.05).

The 10-g monofilament has typically been considered the easiest tool to use for detecting the loss of protective sensation (5,6). However, the 10-g monofilament is only capable of detecting severe DPN, and there is no information on the usefulness of other monofilaments for detecting early DPN. Consistent with studies on micro-neurography, our data show that the 4-g monofilament is clinically useful in the detection of relatively early DPN. Although the sensitivity and specificity of the 4-g monofilament were not sufficient for detecting DPN, this monofilament might be the easiest to apply to the entire diabetic population when factors such as cost, ease of application, and portability are taken into consideration. Because the number of participants was limited, further study is needed to clarify the usefulness of the 4-g monofilament for detecting early DPN.

Footnotes

  • by the American Diabetes Association, Inc.

References

  1. ↵
    American Diabetes Association: Preventive foot care in people with diabetes (Position Statement). Diabetes Care22 (Suppl. 1): S54-S55,1999
    OpenUrlWeb of Science
  2. ↵
    McGill M, Molyneaux L, Spencer R, Heng LF, Yue DK: Possible sources of discrepancies in the use of the Semmes-Weinstein monofilament: impact on prevalence of insensate foot and workload requirements. Diabetes Care 22: 598-602,1999
    OpenUrlAbstract
  3. ↵
    The International Working Group on the Diabetic Foot: Practical Guideline on the Management and the Prevention of the Diabetic Foot. Amsterdam, the Netherlands, The International Working Group on the Diabetic Foot, 1999
  4. ↵
    Hayakawa T: An investigation of diabetic polyneuropathy by microneurography: comparison of the data with motor nerve conduction velocity. J Japan Diab Soc 42:335 -340, 1999
    OpenUrl
  5. ↵
    Kumar S, Fernando DJS, Veves A, Knowles EA, Young MJ, Boulton AMJ: Semmes-Weinstein monofilaments: a simple effective and inexpensive screening device for identifying patients at risk of foot ulceration. Diabetes Res Clin Pract 13:63 -68, 1991
    OpenUrlCrossRefPubMedWeb of Science
  6. ↵
    Birke JA, Rolfsen RJ: Evaluation of a self-administered sensory testing tool to identify patients at risk of diabetes-related foot problems. Diabetes Care 21:23 -25, 1998
    OpenUrlAbstract/FREE Full Text
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4-g Monofilament Is Clinically Useful for Detecting Diabetic Peripheral Neuropathy
Yukihiro Nagai, Yu Sugiyama, Toshio Abe, Gakuji Nomura
Diabetes Care Jan 2001, 24 (1) 183-184; DOI: 10.2337/diacare.24.1.183

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4-g Monofilament Is Clinically Useful for Detecting Diabetic Peripheral Neuropathy
Yukihiro Nagai, Yu Sugiyama, Toshio Abe, Gakuji Nomura
Diabetes Care Jan 2001, 24 (1) 183-184; DOI: 10.2337/diacare.24.1.183
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