Evidence map›Paper›PMID 30934620›Full record

ArticleMedical sciences (Basel, Switzerland)2019

Patterns of Glycemic Variability During a Diabetes Self-Management Educational Program.

Ankur Joshi, Arun Mitra, Nikhat Anjum, Neelesh Shrivastava, Sagar Khadanga, Abhijit Pakhare, Rajnish Joshi

Abstract read
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Article in Medical sciences (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

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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

9 citing papers in PubMed.

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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

7 authors.

Ankur JoshiDepartment of Community and Family Medicine, All India Institute of Medical Sciences (AIIMS), Bhopal 462020 India. ankur.cfm@aiimsbhopal.edu.in.
Arun MitraDepartment of Community and Family Medicine, All India Institute of Medical Sciences (AIIMS), Bhopal 462020 India. dr.arunmitra@gmail.com.ORCID 0000-0001-6742-4033
Nikhat AnjumHospital Services, All India Institute of Medical Sciences, Bhopal 462020, India. nutritionistnikhat@gmail.com.
Neelesh ShrivastavaDepartment of Medicine, All India Institute of Medical Sciences, Bhopal 462020, India. neeleshstv@gmail.com.
Sagar KhadangaDepartment of Medicine, All India Institute of Medical Sciences, Bhopal 462020, India. sagar.genmed@aiimsbhopal.edu.in.
Abhijit PakhareDepartment of Community and Family Medicine, All India Institute of Medical Sciences (AIIMS), Bhopal 462020 India. abhijit.cfm@aiimsbhopal.edu.in.ORCID 0000-0003-2897-4141
Rajnish JoshiDepartment of Medicine, All India Institute of Medical Sciences, Bhopal 462020, India. rajnish.genmed@aiimsbhopal.edu.in.ORCID 0000-0002-4702-0522

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVariations in blood glucose levels over a given time interval is termed as glycemic variability (GV). Higher GV is associated with higher diabetes-related complications. The current study was done with the aim of detecting the sensitivity of various GV indices among individuals with type 2 diabetes mellitus of different glycemic control status.

methodsWe performed a longitudinal study among individuals with type 2 diabetes mellitus (T2DM) who were participating in a two-week diabetes self-management education (DSME) program. Participants were categorized by their HbA1c as poor (≥8%), acceptable (7%⁻8%), and optimal control (<7%). Continuous glucose monitoring (CGM) sensors recorded interstitial glucose every 15 min from day 1. The evaluated GV measures include standard deviation (SD), coefficient of variation (CV), mean amplitude of glycemic excursion (MAGE), continuous overlapping net glycemic action (CONGA), mean of daily difference for inter-day variation (MODD), high blood glucose index (HBGI), and low blood glucose index (LBGI).

resultsA total of 41 study participants with 46347 CGM values were available for analysis. Of 41 participants, 20 (48.7%) were in the poor, 10 (24.3%) in the acceptable, and 11 (26.8%) in the optimal control group. The GV indices (SD; CV; MODD; MAGE; CONGA; HBGI) of poorly controlled (77.43; 38.02; 45.82; 216.63; 14.10; 16.62) were higher than acceptable (50.02; 39.32; 30.79; 138.01; 8.87; 5.56) and optimal (34.15; 29.46; 24.56; 126.15; 8.67; 3.13) control group. Glycemic variability was reduced in the poorly and acceptably controlled groups by the end of the 2-week period. There was a rise in LBGI in the optimally controlled group, indicating pitfalls of tight glycemic control.

conclusionIndices of glycemic variability are useful complements, and changes in it can be demonstrated within short periods.

Indexed as

CONGAglycemic variabilityHBGILBGIMAGEMODD

Identifiers

PMID30934620
PMCPMC6473237

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