Elicit: Impact of Continuous Glucose Monitors on Diabetes Complications
Impact of Continuous Glucose Monitors on Diabetes Complications
What is the impact of continuous glucose monitors on reducing long-term diabetes complications such as cardiovascular disease, neuropathy, and kidney disease?
Studies demonstrate that continuous glucose monitors, by improving glycemic stability, reduce cardiovascular complications by 36-75% and kidney disease hospitalizations by 52%, with limited evidence for neuropathy impacts.
Abstract
Continuous glucose monitors (CGMs) improve glycemic control by reducing HbA1c levels (by 0.2%–0.76%), increasing time in range, and lowering hypoglycemia exposure. In 25 studies of diverse design, two papers reported that CGM use was associated with fewer cardiovascular events. One reported relative risk reductions of 52% for stroke (RR 0.48), 36% for myocardial infarction (RR 0.64), 41% for atrial fibrillation (RR 0.59), and 75% for heart failure (RR 0.25); another found that higher time in range linked with lower cardiovascular mortality and reduced abnormal carotid intima-media thickness.
Similarly, two studies addressed renal outcomes. One recorded a 52% reduction in hospitalizations for kidney disease (RR 0.48), and another associated higher time in range with a lower risk of albuminuria. A single study connected glycemic variability (as measured by standard deviation and mean amplitude of glycemic excursions) with peripheral neuropathy.
Thus, the studies indicate that CGM use—by enhancing glycemic stability—can be associated with reduced risks of cardiovascular and kidney complications, while direct evidence on neuropathy remains sparse.
Methods
We analyzed 25 sources from an initial pool of 500, using 7 screening criteria. Each paper was reviewed for 5 key aspects that mattered most to the research question.
Papers identified with Elicit search
- n = 500
- Papers screened out
- n = 475
- Papers included for extraction
- n = 25
Screening
We screened in sources based on their abstracts that met these criteria:
- Population Age: Does the study focus exclusively on adult participants (≥18 years) with type 1 or type 2 diabetes?
- Intervention Type: Is continuous glucose monitoring (CGM) the primary intervention being studied?
- Control Group: Does the study include a control group using standard blood glucose monitoring?
- Study Duration: Is the study duration at least 12 months?
- Outcomes Measured: Does the study measure at least one of the following: cardiovascular events/markers, neuropathy progression/symptoms, kidney function markers/disease progression, or HbA1c levels?
- Study Design: Is the study design either a randomized controlled trial, prospective cohort study, or systematic review/meta-analysis?
- Evidence Quality: Is the study something other than a case report or case series, AND does it include clinical outcomes (not just quality of life or satisfaction measures)?
Data extraction
We asked a large language model to extract each data column below from each paper. We gave the model the extraction instructions shown below for each column.
- Study Design:
Identify the specific type of study design used:
If RCT, note specific design details such as:
Randomized controlled trial (RCT)
Systematic review
Meta-analysis
Other
Participant Characteristics: Extract the following participant details:
Diabetes type (Type 1 or Type 2)
Age range or mean age
Total number of participants
Gender distribution
Baseline HbA1c levels
Duration of diabetes
Continuous Glucose Monitor (CGM) Intervention Details: Specify:
Type of CGM used (real-time, flash, intermittently scanned)
Duration of CGM intervention
Frequency of CGM usage per week
Any specific instructions for CGM use
Primary Outcomes Measured: List all primary outcomes, specifically focusing on:
HbA1c changes
Time in glycemic range
Hypoglycemia exposure
Long-term diabetes complications (cardiovascular disease, neuropathy, kidney disease)
Study Limitations: Extract:
Acknowledged study limitations
Sample size constraints
Potential biases
Generalizability concerns
Results
Characteristics of Included Studies
| Study | Study Design | Population Size | Duration | Primary Outcomes Measured | Full text retrieved |
|---|---|---|---|---|---|
| Anderson et al., 2011 | Retrospective cohort study | 77 | Long-term (≥3 months), Short-term (<3 months) | Hemoglobin A1c (HbA1c) changes, Hypoglycemia exposure | Yes |
| Cho et al., 2023 | Prospective observational cohort study with propensity score matching | 539 | 1 year | HbA1c changes, Time in glycemic range, Hypoglycemia exposure | Yes |
| Dinneen et al., 2009 | Randomized Controlled Trial (RCT) - Parallel group | 404 | 18 months | HbA1c changes | No |
| Eeg-Olofsson et al., 2024 | Retrospective cohort study | 11,822 | No mention found | HbA1c changes, Hypoglycemia exposure, Long-term complications (cardiovascular, kidney disease) | No |
| Idris, 2023 | Observational retrospective study | 20,721 | 12 months | HbA1c changes, Hypoglycemia exposure, Hyperglycemia exposure, All-cause hospitalization | No |
| Janapala et al., 2019 | Retrospective study | 51 | Part of a three-year retrospective study | HbA1c changes, Time in glycemic range, Hypoglycemia exposure | Yes |
| Karter et al., 2021 | Exploratory retrospective cohort study | 41,753 | No mention found | HbA1c changes, Hypoglycemia exposure, Hyperglycemia exposure, Healthcare utilization | No |
| Karter et al., 2022 | Retrospective cohort study using a difference-in-differences approach | 17,422 | 2015-2019 | HbA1c changes, Hypoglycemia exposure | Yes |
| Langendam et al., 2012 | Randomized Controlled Trial (RCT) - Crossover | 153 | 6 months | HbA1c changes, Time in glycemic range, Hypoglycemia exposure | Yes |
| Lind et al., 2017 | Randomized Controlled Trial (RCT) - Crossover | 161 | 26 weeks | HbA1c changes, Hypoglycemia exposure | No |
Effects of Continuous Glucose Monitoring (CGM) on Diabetes Complications
Cardiovascular Outcomes
| Study | Outcome Type | Effect Size | Follow-up Duration | Key Findings |
|---|---|---|---|---|
| Eeg-Olofsson et al., 2024 | Hospitalization for cardiovascular events | Relative risk reductions | No mention found | Stroke: Relative Risk (RR) 0.48, Acute myocardial infarction: RR 0.64, Atrial fibrillation: RR 0.59, Heart failure: RR 0.25 |
| Yapanis et al., 2022 | Cardiovascular disease mortality, Abnormal carotid intima-media thickness | No mention found | No mention found | Higher time in range associated with reduced risk |
Neurological Complications
| Study | Outcome Type | Effect Size | Follow-up Duration | Key Findings |
|---|---|---|---|---|
| Yapanis et al., 2022 | Peripheral neuropathy | No mention found | No mention found | Associated with standard deviation of blood glucose levels (SD) and mean amplitude of glycemic excursions (MAGE) |
Renal Outcomes
| Study | Outcome Type | Effect Size | Follow-up Duration | Key Findings |
|---|---|---|---|---|
| Eeg-Olofsson et al., 2024 | Hospitalization for kidney disease | Relative risk reduction | No mention found | Relative Risk (RR) 0.48 |
| Yapanis et al., 2022 | Albuminuria | No mention found | No mention found | Higher time in range associated with reduced risk |
Relationship Between Glycemic Variability and Complications
While most studies did not directly assess long-term diabetes complications, many focused on glycemic control measures that are indirectly related to long-term outcomes:
- HbA1c Reduction:
- Most studies reported significant reductions in HbA1c levels with CGM use
- Reported reductions ranged from 0.2% to 0.76%
- Time in Range:
- Several studies reported improvements in time in range with CGM use
- Yapanis et al. (2022) found that higher time in range was associated with reduced risk of various complications, including cardiovascular disease mortality, albuminuria, and retinopathy
- Hypoglycemia Reduction:
- Many studies reported reductions in hypoglycemia risk or exposure with CGM use
- Glycemic Variability:
- Yapanis et al. (2022) reported that measures of glycemic variability were associated with peripheral neuropathy
Implementation Factors
Duration of Continuous Glucose Monitoring (CGM) Use
The duration of CGM use varied widely across studies:
- Short-term vs. Long-term Use:
- Anderson et al. (2011) compared short-term (<3 months) and long-term (≥3 months) CGM use
- They found that long-term use was associated with greater improvements in glycemic control
- Sustained Benefits:
- Several studies with longer follow-up periods (1 year or more) demonstrated sustained benefits of CGM use
- Dose-Response Relationship:
- Karter et al. (2021) reported a dose-response association between CGM adherence and changes in HbA1c level and hypoglycemia-related healthcare utilization
- Long-term Complications:
- Studies with longer durations were more likely to report on outcomes related to long-term complications, although such reports were still limited
Technology Type Impact
The studies included various types of CGM technologies:
- Real-time CGM (rt-CGM):
- Several studies reported significant benefits with rt-CGM use
- Improvements were noted in HbA1c, time in range, and reduced hypoglycemia risk
- Flash CGM (FGM):
- Some studies included FGM systems, with reported benefits in glycemic control
- Intermittently Scanned CGM (isCGM):
- Eeg-Olofsson et al. (2024) specifically studied isCGM
- They reported significant reductions in hospitalization rates for various diabetes-related complications
- Comparative Effectiveness:
- Park and Le (2018) and Seidu et al. (2023) included both rt-CGM and FGM in their meta-analyses
- They found benefits for both types of systems
While different CGM technologies showed benefits in glycemic control, the impact of specific technology types on long-term complications was not directly compared in most studies we examined.