Evidence map›Paper›PMID 29372050›Full record

ArticleJournal of nutritional science2018

Improvement of glucose and lipid metabolism via mung bean protein consumption: clinical trials of GLUCODIA™ isolated mung bean protein in the USA and Canada.

Mitsutaka Kohno, Hideo Sugano, Yuhko Shigihara, Yoshiaki Shiraishi, Takayasu Motoyama

Abstract read
In one paragraph

Article in Journal of nutritional science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Mung Bean (Nutrients · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Mitsutaka KohnoFuji Oil Holdings Inc., R&D Division for Future Creation, 4-3 Kinunodai, Tsukubamirai, Ibaraki 300-2497, Japan.
Hideo SuganoFuji Oil Holdings Inc., R&D Division for Future Creation, 4-3 Kinunodai, Tsukubamirai, Ibaraki 300-2497, Japan.
Yuhko ShigiharaFuji Oil Holdings Inc., R&D Division for Future Creation, 4-3 Kinunodai, Tsukubamirai, Ibaraki 300-2497, Japan.
Yoshiaki ShiraishiJ-PORT Company, 166 Georgetown Drive, Mountain View, CA 94043, USA.
Takayasu MotoyamaFuji Oil Holdings Inc., R&D Division for Future Creation, 4-3 Kinunodai, Tsukubamirai, Ibaraki 300-2497, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to confirm the effects of a commercially available mung bean protein isolate (GLUCODIA™) on glucose and lipid metabolism. The main component of GLUCODIA™ is 8S globulin, which constitutes 80 % of the total protein. The overall structure of this protein closely resembles soyabean β-conglycinin, which accounts for 20 % of total soya protein (soya protein isolate; SPI). Many physiological beneficial effects of β-conglycinin have been reported. GLUCODIA™ is expected to produce beneficial effects with fewer intakes than SPI. We conducted two independent double-blind, placebo-controlled clinical studies. In the first (preliminary dose decision trial) study, mung bean protein was shown to exert physiological beneficial effects when 3·0 g were ingested per d. In the second (main clinical trial) study, mung bean protein isolate did not lower plasma glucose levels, although the mean insulin level decreased with consumption of mung bean protein. The homeostatic model assessment of insulin resistance (HOMA-IR) values significantly decreased with mung bean protein. The mean TAG level significantly decreased with consumption of mung bean protein isolate. A significant increase in serum adiponectin levels and improvement in liver function enzymes were observed. These findings suggest that GLUCODIA™ could be useful in the prevention of insulin resistance and visceral fat accumulation, which are known to trigger the metabolic syndrome, and in the prevention of liver function decline.

Indexed as

AE, adverse eventALT, alanine aminotransferaseFPG, fasting plasma glucoseHepatic function enzymesHOMA-IR, homeostatic model assessment of insulin resistanceHomeostatic model assessment of insulin resistanceInsulinMung bean proteinMuPI, mung bean protein isolateSerum TAGSPI, soya protein isolate

Identifiers

PMID29372050
PMCPMC5773921

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.