Advertisement

High-Viscosity Hydroxypropylmethylcellulose Blunts Postprandial Glucose and Insulin Responses

  1. Kevin C. Maki, PHD1,
  2. Michael L. Carson, DO, MPH2,
  3. Marvin P. Miller, PHD2,
  4. Maciej Turowski, PHD2,
  5. Marjorie Bell, BS1,
  6. Donna M. Wilder, BS, MT(ASCP)1 and
  7. Matthew S. Reeves, DO1
  1. 1Provident Clinical Research, Bloomington, Indiana
  2. 2Dow Chemical Company, Midland, Michigan
  1. Address correspondence and reprint requests to Kevin C. Maki, PhD, Provident Clinical Research, 1000 W. 1st St., Bloomington, IN 47403. E-mail: kmaki{at}providentcrc.com

Abstract

OBJECTIVE—High-viscosity hydroxypropylmethylcellulose (HV-HPMC) is a modified cellulose fiber that produces a viscous gel in the gastrointestinal tract. Clinical trials demonstrate that consumption of HV-HPMC significantly lowers cholesterol, but limited information has been available on the influence of HV-HPMC on postprandial insulin and glucose responses. The objective of this investigation was to assess the influence of HV-HPMC on postprandial glucose and insulin responses in overweight and obese men and women.

RESEARCH DESIGN AND METHODS—Participants were 31 overweight or obese men and women without diabetes who underwent three breakfast meal tests in random order, separated by ≥72 h. Test meals containing 75 g carbohydrate plus 4 or 8 g HV-HPMC or control meals containing 8 g cellulose were delivered in a double-blind fashion.

RESULTS—Peak glucose was significantly lower (P < 0.001) after both HV-HPMC–containing meals (7.4 mmol/l [4 g] and 7.4 mmol/l [8 g]) compared with the control meal (8.6 mmol/l). Peak insulin concentrations and the incremental areas for glucose and insulin from 0 to 120 min were also significantly reduced after both HV-HPMC doses versus control (all P < 0.01).

CONCLUSIONS—These findings indicate that HV-HPMC consumption reduces postprandial glucose and insulin excursions, which may favorably alter risks for diabetes and cardiovascular disease.

Footnotes

  • Published ahead of print at http://care.diabetesjournals.org on 24 January 2007. DOI: 10.2337/dc06-2344.

    A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.

    • Accepted January 16, 2007.
    • Received November 15, 2006.
| Table of Contents

This Article

  1. Diabetes Care vol. 30 no. 5 1039-1043
  1. Erratum
  2. All Versions of this Article:
    1. dc06-2344v1
    2. 30/5/1039 most recent
Advertisement