Evidence map›Paper›PMID 33161904›Full record

Trial reportThe British journal of nutrition2021

Blackcurrant (

Jenni Lappi, Kaisa Raninen, Kati Väkeväinen, Anna Kårlund, Riitta Törrönen, Marjukka Kolehmainen

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The British journal of nutrition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% of its field
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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. The Current State of Knowledge onPlants (Basel, Switzerland) · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Potential Vasculoprotective Effects of Blackcurrant (Molecules (Basel, Switzerland) · 2021
    Article
  9. Article
  10. 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

6 authors at 2 institutions in 1 country.

Jenni LappiFaculty of Business, Tourism and Hospitality, Savonia University of Applied Sciences, 70201Kuopio, Finland.
Kaisa RaninenInstitute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211Kuopio, Finland.
Kati VäkeväinenInstitute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211Kuopio, Finland.
Anna KårlundInstitute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211Kuopio, Finland.
Riitta TörrönenInstitute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211Kuopio, Finland.
Marjukka KolehmainenInstitute of Public Health and Clinical Nutrition, University of Eastern Finland, 70211Kuopio, Finland.ORCID 0000-0002-3770-2538
University of Eastern Finland · FISavonia University of Applied Sciences · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Berries rich in anthocyanins have beneficial effects on postprandial glycaemia. We investigated whether blackcurrant (75 g in a portion) independently and in a product with fermented quinoa induced similar effects on the sugar-induced postprandial glucose metabolism as observed before with 150 g of blackcurrant. Twenty-six healthy subjects (twenty-two females and four males) consumed four test products after fasting overnight in a randomised, controlled crossover design. Each test product portion contained 31 g of available carbohydrates and had similar composition of sugar components: 300 ml water with sucrose, glucose and fructose (SW; reference), blackcurrant purée with added sugars (BC), a product consisting of the blackcurrant purée and a product base with fermented quinoa (BCP) and the product base without blackcurrant (PB). Blood samples were collected at 0, 15, 30, 45, 60, 90, 120 and 180 min after eating each test product to analyse the concentrations of glucose, insulin and NEFA. In comparison with the SW, the intake of both the BC and BCP resulted in reduced glucose and insulin concentrations during the first 30 min, a more balanced decline during the first hour and improved glycaemic profile. The BCP induced more efficient effects than the BC due to the product base with fermented quinoa. A rebound of NEFA after the sugar-induced hypoglycaemic response was attenuated at the late postprandial phase by the BC and BCP. In conclusion, we showed that 75 g of blackcurrant and the product with fermented quinoa were able to lower postprandial glycaemia and insulinaemia.

Indexed as

Chenopodium quinoaFruitGlycemic ControlPostprandial PeriodRibesAnthocyaninsBlood GlucoseCross-Over StudiesFatty Acids, NonesterifiedFemaleHumansInsulinMaleSugarsAnthocyaninsBlood GlucoseFatty Acids, NonesterifiedInsulinSugarsBlackcurrantsFermented quinoaFood productsGlycaemiaPostprandial metabolism

Identifiers

PMID33161904
PMCPMC8340457
OpenAlexW3098747181

What Socratic 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 Socratic graph.