Evidence map›Paper›PMID 26536491›Full record

ArticleDiabetic medicine : a journal of the British Diabetic Association2016

Postprandial capillary-venous glucose gradient in Type 1 diabetes: magnitude and clinical associations in a real world setting.

I Lee, H Lunt, H Chan, H Heenan, J Berkeley, C M A Frampton

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Article in Diabetic medicine : a journal of the British Diabetic Association, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Capillary Samples and Hemolysis: Further Considerations.Journal of diabetes science and technology · 2017
    Article
  6. Article
4 · The record

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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.

I LeeSchool of Medicine, University of Otago, Christchurch, New Zealand.
H LuntDepartment of Medicine, University of Otago, Christchurch, New Zealand.
H ChanCanterbury District Health Board, Christchurch Diabetes Centre, Christchurch, New Zealand.
H HeenanCanterbury District Health Board, Christchurch Diabetes Centre, Christchurch, New Zealand.
J BerkeleyCanterbury District Health Board, Christchurch Diabetes Centre, Christchurch, New Zealand.
C M A FramptonDepartment of Medicine, University of Otago, Christchurch, New Zealand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTo determine the magnitude of the peripheral glucose gradient in patients with Type 1 diabetes in a real world setting and to explore its relationship with insulin dose and macronutrient intake.

methodsAll patients used mealtime analogue insulin. The glucose gradient was assessed using antecubital fossa venous and finger-stick capillary samples, collected concurrently at room temperature. Baseline sampling occurred before the administration of an insulin dose and breakfast of the patient's choosing. Breakfast was consumed an average of 15 min after baseline. The macronutrient content of breakfast was documented. Sampling was repeated 1 and 2 h after baseline.

resultsThe mean (95% CI) plasma capillary-venous glucose gradient values for 43 patients were: pre-breakfast, 0.21 (0.08-0.34) mmol/l; 1 h after baseline, 0.87 (0.66-1.07) mmol/l; and 2 h after baseline, 0.52 (0.33-0.71) mmol/l. Glucose gradient and dietary carbohydrate intake (g/kg body weight) were positively correlated at both 1 h (P < 0.01) and 2 h after baseline (P < 0.01). No relationship was observed between this gradient and mealtime insulin dose, or the glucose concentration at either time point.

conclusionsIn patients with Type 1 diabetes, a clinically significant glucose gradient is present after the ingestion of a carbohydrate-rich meal. As postprandial capillary and venous plasma glucose concentrations are not equivalent, defining the site of sample collection is important.

Indexed as

CapillariesPostprandial PeriodVeinsAdultAgedAged, 80 and overBlood GlucoseBlood Specimen CollectionDiabetes Mellitus, Type 1Dietary CarbohydratesFemaleHumansHypoglycemic AgentsInsulinMaleMiddle AgedBlood GlucoseDietary CarbohydratesHypoglycemic AgentsInsulin

Identifiers

PMID26536491
PMCPMC5064751

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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.