Journal of Clinical Lipidology
Volume 3, Issue 3 , Pages 159-166, May 2009

Lipid-altering effects of different formulations of hydroxypropylmethylcellulose

  • Kevin C. Maki, PhD

      Affiliations

    • Provident Clinical Research, Bloomington, Indiana, USA
    • Provident Clinical Research, 489 Taft Avenue, Glen Ellyn, Illinois, USA
    • Corresponding Author InformationCorresponding author.
  • ,
  • Michael L. Carson, DO, MPH

      Affiliations

    • The Dow Chemical Company, Midland, Michigan, USA
  • ,
  • W.H. Kerr Anderson, PhD

      Affiliations

    • The Dow Chemical Company, Midland, Michigan, USA
  • ,
  • Jeffrey Geohas, MD

      Affiliations

    • Radiant Research, Chicago, Illinois, USA
  • ,
  • Matthew S. Reeves, DO

      Affiliations

    • Provident Clinical Research, Bloomington, Indiana, USA
  • ,
  • Mildred V. Farmer, MD

      Affiliations

    • Meridien Research, St. Petersburg, Florida, USA
  • ,
  • Maciej Turowski, PhD

      Affiliations

    • The Dow Chemical Company, Midland, Michigan, USA
  • ,
  • Marvin Miller, PhD

      Affiliations

    • The Dow Chemical Company, Midland, Michigan, USA
  • ,
  • Valerie N. Kaden

      Affiliations

    • Provident Clinical Research, 489 Taft Avenue, Glen Ellyn, Illinois, USA
  • ,
  • Mary R. Dicklin, PhD

      Affiliations

    • Provident Clinical Research, 489 Taft Avenue, Glen Ellyn, Illinois, USA
  • ,
  • Tia M. Rains, PhD

      Affiliations

    • Provident Clinical Research, 489 Taft Avenue, Glen Ellyn, Illinois, USA

Received 3 February 2009; accepted 30 April 2009. published online 06 May 2009.

Background

Hydroxypropylmethylcellulose (HPMC), a viscous, soluble dietary fiber, has been shown to be efficacious for lowering total and low-density lipoprotein cholesterol (LDL-C) concentrations. The relative effects of various dosages and viscosities of HPMC have not been fully evaluated.

Objective

To examine the lipid-altering effects of several formulations of HPMC.

Methods

In this randomized, double-blind pilot study, 165 men and women with primary hypercholesterolemia consumed a control product (snack bar or drink mix) or an HPMC-containing test bar or drink for 4 weeks. HPMC-containing products delivered 3, 5, or 10g of HPMC of low, moderate, moderately high, or high viscosity (9 HPMC groups, each with ∼15 subjects).

Results

Data from drink and bar groups were combined because there was no evidence of a vehicle effect. The resulting analysis included data from the control and 6 HPMC dose and viscosity combinations. All HPMC groups showed LDL-C reductions ranging from 6.1 to 13.3% (P < .05 vs. baseline for 6 of the 7 groups), compared with a nonsignificant reduction (1.9%) in the control group. Changes in total and non-high-density lipoprotein cholesterol paralleled those for LDL-C. Concentrations of high-density lipoprotein cholesterol, triglycerides, apolipoprotein B, and high-sensitivity C-reactive protein were not significantly altered.

Conclusion

This pilot study provides preliminary evidence to support the efficacy of various formulations of HPMC for reducing cholesterol carried by atherogenic particles in men and women with primary hypercholesterolemia. Additional research will be required to more clearly define the roles of viscosity and dosage on the lipid-altering effects of HPMC.

Keywords: Hydroxypropylmethylcellulose, Hypercholesterolemia, Lipids, Low-density lipoprotein cholesterol, Viscous dietary fiber

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PII: S1933-2874(09)00200-1

doi:10.1016/j.jacl.2009.04.053

Journal of Clinical Lipidology
Volume 3, Issue 3 , Pages 159-166, May 2009