AI Article Synopsis

  • - Chronic hyperglycaemia in type 2 diabetes (T2DM) leads to vascular damage, and glycaemic variability (GV) plays a significant role in worsening health outcomes, though continuous glucose monitoring (CGM) data isn't widely used yet in T2DM management.
  • - A literature review was conducted to find high-level evidence linking GV metrics to vascular and clinical complications in T2DM, while excluding lower-quality studies that weren't as reliable.
  • - Six studies showed some association between GV indices (like standard deviation and time in range) and clinical issues, but results should be taken cautiously due to the moderate to low quality of the studies; more extensive and diverse research is needed to confirm these findings.

Article Abstract

(1) Background: Chronic hyperglycaemia is a cause of vascular damage and other adverse clinical outcomes in type 2 diabetes mellitus (T2DM). Emerging evidence suggests a significant and independent role for glycaemic variability (GV) in contributing to those outcomes. Continuous glucose monitoring (CGM) provides valuable insights into GV. Unlike in type 1 diabetes mellitus, the use of CGM-derived GV indices has not been widely adopted in the management of T2DM due to the limited evidence of their effectiveness in predicting clinical outcomes. This study aimed to explore the associations between GV metrics and short- or long-term vascular and clinical complications in T2DM. (2) Methods: A rapid literature review was conducted using the Cochrane Library, MEDLINE, and Scopus databases to seek high-level evidence. Lower-quality studies such as cross-sectional studies were excluded, but their content was reviewed. (3) Results: Six studies (five prospective cohort studies and one clinical trial) reported associations between GV indices (coefficient of variation (CV), standard deviation (SD), Mean Amplitude of Glycaemic Excursions (MAGE), Time in Range (TIR), Time Above Range (TAR), and Time Below Range (TBR)), and clinical complications. However, since most evidence came from moderate to low-quality studies, the results should be interpreted with caution. (4) Conclusions: Limited but significant evidence suggests that GV indices may predict clinical compilations in T2DM both in the short term and long term. There is a need for longitudinal studies in larger and more diverse populations, longer follow-ups, and the use of numerous CGM-derived GV indices while collecting information about all microvascular and macrovascular complications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11312427PMC
http://dx.doi.org/10.3390/healthcare12151542DOI Listing

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