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Review Article
Diabetes, Obesity and Metabolism Recent Updates to Clinical Practice Guidelines for Diabetes Mellitus
Jin Yu1orcid, Seung-Hwan Lee1,2orcid, Mee Kyoung Kim3orcid
Endocrinology and Metabolism 2022;37(1):26-37.
DOI: https://doi.org/10.3803/EnM.2022.105
Published online: February 28, 2022

1Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

2Department of Medical Informatics, College of Medicine, The Catholic University of Korea, Seoul, Korea

3Division of Endocrinology and Metabolism, Department of Internal Medicine, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

Corresponding authors: Seung-Hwan Lee. Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea, Tel: +82-2-2258-6069, Fax: +82-2-595-2534, E-mail: hwanx2@catholic.ac.kr
Mee Kyoung Kim. Division of Endocrinology and Metabolism, Department of Internal Medicine, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 10 63-ro, Yeongdeungpo-gu, Seoul 07345, Korea, Tel: +82-2-3779-1368, Fax: +82-2-595-2534, E-mail: makung@catholic.ac.kr
• Received: January 24, 2022   • Revised: January 31, 2022   • Accepted: February 6, 2022

Copyright © 2022 Korean Endocrine Society

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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  • Guidelines for the management of patients with diabetes have become an important part of clinical practice that improve the quality of care and help establish evidence-based medicine in this field. With rapidly accumulating evidence on various aspects of diabetes care, including landmark clinical trials of treatment agents and newer technologies, timely updates of the guidelines capture the most current state of the field and present a consensus. As a leading academic society, the Korean Diabetes Association publishes practice guidelines biennially and the American Diabetes Association does so annually. In this review, we summarize the key changes suggested in the most recent guidelines. Some of the important updates include treatment algorithms emphasizing comorbid conditions such as atherosclerotic cardiovascular disease, heart failure, and chronic kidney disease in the selection of anti-diabetic agents; wider application of continuous glucose monitoring (CGM), insulin pump technologies and indices derived from CGM such as time in range; more active screening of subjects at high-risk of diabetes; and more detailed individualization in diabetes care. Although there are both similarities and differences among guidelines and some uncertainty remains, these updates provide a good approach for many clinical practitioners who are battling with diabetes.
  • Keywords: Diabetes mellitus, type 2; Consensus; Evidence-based medicine; Blood glucose
The field of diabetes care is changing rapidly. Based on accumulating evidence on diverse aspects of diabetes management, clinical practice guidelines are updated in a timely manner. In particular, some landmark clinical trials on newer anti-diabetic medications are changing the landscape of treatment strategies. Technological advances are also being applied for glucose monitoring and insulin treatment. Therefore, in this review, we summarize the major guidelines that have been updated recently and compare the differences between these guidelines.
The Committee of Clinical Practice Guidelines of the Korean Diabetes Association (KDA) updated the previous clinical practice guidelines for Korean adults with diabetes and published the seventh edition in May 2021 [1]. The updated statements endorsed a glycosylated hemoglobin (A1C) target of 6.5% for type 2 diabetes mellitus (DM) if it can be achieved safely [1]. In adults with recently diagnosed type 2 DM and no clinically significant cardiovascular disease (CVD), glycemic control aimed at the near-normal range should be considered, with the aim of preventing the development of microvascular and macrovascular complications over the lifetime, if this goal can be achieved without substantial hypoglycemia or other unacceptable adverse consequences [1]. Table 1 summarizes the goal of glucose, blood pressure, and lipid control for patients with type 2 DM according to the KDA guidelines compared with other guidelines.
The treatment algorithm stratifies the strategy of glycemic control for type 2 DM based on initial A1C levels and underlying comorbidities (Fig. 1). The largest change is more aggressive guidance that first recommends the use of specific drugs in patients with a specific disease or high-risk, deviating from the previous recommendations to start with metformin. The revised guidelines emphasize that injectable drugs are not the final treatment that is selected when there is no other option, but an option that should be considered in any circumstances.
After the initiation of therapy with a glucose-lowering agent, monotherapy or combination therapy should be provided on the basis of the target and current A1C levels. Initial combination therapy is recommended if the current A1C is 1.5% to 2.0% higher than the target A1C. Insulin treatment should be prioritized if the baseline A1C is ≥9% and the patient is symptomatic (e.g., polydipsia, polyuria, or weight loss). It is recommended to consider any associated comorbidities (heart failure, established CVD, or chronic kidney disease [CKD]) when selecting a glucose-lowering agent. Regimens that include sodium-glucose cotransporter 2 (SGLT2) inhibitors or glucagon-like peptide 1 receptor agonists (GLP-1 RAs) with proven cardiovascular (CV) benefits should be prioritized for combination therapy in patients with established atherosclerotic cardiovascular disease (ASCVD) [2–10]. For patients with heart failure, SGLT2 inhibitors with proven CV benefits, should be prioritized [2–10]. For patients with albuminuria or reduced kidney function, SGLT2 inhibitors with proven renal and CV benefits should be prioritized [9,10]. Apart from recommending metformin as the first-line agent, SGLT2 inhibitors or GLP-1 RAs are recommended as first-line agents if there is a comorbidity such as ASCVD [1].
This updated guideline has new sections on continuous glucose monitoring (CGM), insulin pump use, and non-alcoholic fatty liver disease (NAFLD) in patients with DM. Thiazolidinedione or GLP-1 RAs can be used for the treatment of NAFLD in adults with type 2 DM, while metformin, dipeptidyl peptidase 4 inhibitors, vitamin E, and statins are not recommended for the treatment of NAFLD [11–13]. All adult type 1 DM patients should be encouraged to use real-time CGM devices to control blood glucose and lower the risk of hypoglycemia [14,15]. In addition, it has been suggested that adults with type 2 DM who require multiple daily injections may use real-time CGM devices for glycemic control [14,15]. To reduce the risk of severe hypoglycemia for adult patients with type 1 DM who experience severe hypoglycemia, insulin pumps, rather than multiple daily injections, are recommended even in the absence of CGM.
The American Association of Clinical Endocrinology (AACE) published an updated guideline for available advanced diabetes technology in 2021 without updating their other guidelines on comprehensive type 2 diabetes management [16,17]. Clinical practice guidelines for this rapidly evolving field, encompassing CGM, insulin pump management, and the integration of CGM and pump therapy, have also been published. According to the AACE guideline on new diabetes technology, CGM is recommended for all people with diabetes treated with intensive insulin therapy, defined as three or more injections per day or use of an insulin pump [16,17].
Real-time CGM is recommended over intermittently scanned CGM for people with diabetes with problematic hypoglycemia who require predictive alarms [18–20]. Guidance on the CGM metrics for clinical decision-making is also included, according to which two metrics—time in range (TIR) and time below range (TBR)—should be used as the starting point for the assessment of the quality of glycemic control and as the basis for therapy adjustment, with an emphasis on reducing TBR when the percentages of CGM values falling below 54 or 70 mg/dL exceed targets (Table 2) [21]. These guidelines emphasize the need to check first by focusing on hypoglycemia (TBR) [16].
During the past decade, manufacturers have integrated CGM into pump technologies across a wide spectrum of devices, from sensor-augmented insulin pumps to low-glucose suspend and predictive low-glucose suspend systems to hybrid closed-loop systems, which are referred to as automated insulin dosing (AID) systems. Advances in technology have led to the development of AID systems, which have the ability to increase basal insulin delivery to address hyperglycemia, in addition to suspending insulin infusion to mitigate hypoglycemia. AID systems are strongly recommended for all people with type 1 DM, since their use has been shown to increase TIR, especially in the overnight period, without causing an increased risk of hypoglycemia [16,22,23]. Given improvements in TIR and the reduction in hyperglycemia with AID systems, this method of insulin delivery is preferred above other modalities. AID systems should be considered for people with diabetes who have suboptimal glycemia, significant glycemic variability, or impaired hypoglycemia awareness, or in whom permissive hyperglycemia is allowed due to the fear of hypoglycemia.
The American Diabetes Association (ADA) releases updated Standards of Medical Care in Diabetes every year in January [24]. Recent updates have focused on individualization of diabetes management in screening, intervention and care, use of technology, and prevention of complications [25]. Patient-centered care goals were emphasized in preventing type 2 DM. Overweight and obese adults at high-risk of type 2 DM are recommended to be referred to an intensive lifestyle and behavior change program. Individualized management of overweight and obese adults was also emphasized to prevent diabetes and comorbidities [26]. With developments of technology, it was recommended to consider technological assistance according to the individual’s preference [27].
According to the most recent recommendations, screening for prediabetes and diabetes should begin at the age of 35 years [26]. The previous recommendation was that testing should begin at the age of 45 years. This change reflects the findings that opportunistic universal screening among individuals aged ≥35 years could greatly reduce the national prevalence of undiagnosed prediabetes or diabetes at a relatively low cost. In the glycemic assessment section, TIR along with A1C has been more fully incorporated into the guideline [27]. A 14-day CGM assessment of TIR and use of a glucose management indicator can serve as a surrogate for A1C in clinical management.
The use of metformin as the first-line therapy did not change, but individualization of treatment was emphasized. Although previous guidelines recommended the use of SGLT2 inhibitors and GLP-1 RAs in patients with CVD and/or CKD, the updated guideline recommends these treatments earlier [28]. In addition, the updated guideline reflects the adjustment to patient-centered treatment goals rather than sequential treatment to intensify treatment [29]. In the case of using insulin, GLP-1 RA combination therapy is still recommended, but it emphasizes combination therapy earlier [30–34].
In the diabetes care section, a comprehensive approach to reduce complications is recommended. Therapy includes management of glycemia, blood pressure, and lipids and the incorporation of treatment with benefits for CVD and/or CKD outcomes [35]. Patients with type 2 diabetes and ASCVD are recommended to use SGLT2 inhibitors and/or GLP-1RAs [2,4,10]. Patients with type 2 diabetes and established heart failure with a reduced ejection fraction are recommended to use SGLT2 inhibitors, as this class of medications has proven benefits for reducing heart failure and CV death [8,36]. Additional data on the benefits of SGLT2 inhibitors in decompensated heart failure and heart failure with preserved ejection fraction have been included in the updates [37,38]. The updated guideline recommends SGLT2 inhibitors in patients with stage 3 CKD or higher and type 2 diabetes regardless of glycemic control [39]. For patients with type 2 diabetes and diabetic kidney disease, the use of SGLT2 inhibitors in patients with an estimated glomerular filtration rate of ≥25 mL/min/1.73 m2 and urinary albumin ≥300 mg/g creatinine is recommended to reduce CKD progression and CVD [7,9,10, 40]. GLP-1 RAs are also suggested for patients with CV risk to slow CKD progression [9]. A new recommendation is to use finerenone, a nonsteroidal mineralocorticoid receptor antagonist, to reduce CKD progression and CV events when it is not possible to use SGLT2 inhibitors [41,42].
The updates to the guideline include an extensive discussion of technology. The term “diabetes technology” is used to describe the hardware, devices, and software used to help diabetes patients manage their condition. The updates state that the individualization of technology type and selection is necessary both to prevent diabetes and to manage diabetes patients. Related education and evaluation of usage should also be conducted periodically [27]. The important point in the updates is that the active use of CGM devices has been added. The active use of CGM devices is now recommended from the early stage of diagnosis of diabetes requiring insulin management. In previous guidelines, CGM devices were only recommended for patients requiring multiple daily injections or continuous subcutaneous insulin infusion, but this year’s recommendation extends to long-acting insulin (basal insulin) users [43,44]. The use of CGM devices is also recommended for children with diabetes using insulin, and AID systems are recommended for children with type 1 diabetes. For this reason, the importance of diabetes management in schools is mentioned in the guideline [45]. Because of the coronavirus disease 2019 pandemic, CGM devices have been widely used to minimize contact between health care providers and patients [46–52]. This situation is expected to advance the management of diabetes using technology.
Due to the challenges of managing type 1 diabetes and advances in new treatments and technologies, the ADA and European Association for the Study of Diabetes published a consensus report on type 1 diabetes management in October 2021 [53]. An important point in diagnosing type 1 diabetes is to distinguish it from type 2 diabetes and monogenic diabetes. Distinguishing features include younger age (<35 years), lower BMI (<25 kg/m2), weight loss, ketoacidosis, and glucose ≥360 mg/dL at diagnosis [54]. Rapid progression to insulin treatment (<3 years) is strongly suggestive of type 1 diabetes at any age [55–57]. Beyond 3 years after diagnosis, if there is uncertainty about diabetes type, a random C-peptide measurement with concurrent glucose within 5 hours of eating is recommended [53].
To prevent the development and progression of diabetes complications, it is necessary to maintain glucose levels within an individual’s target range. To maintain glucose levels, the effective delivery of exogenous insulin and appropriate indications of glucose levels are important [53]. A1C is an indicator of mean glucose levels, but it does not reflect glycemic variability and hypoglycemia [58,59]. Therefore, capillary blood glucose monitoring plays an important role. According to this report, CGM is the standard method for glucose monitoring (Fig. 2). However, frequent blood glucose monitoring measurements are emphasized in the integrative management of diabetes, regardless of CGM use, because there are concerns that CGM readings do not reflect plasma glucose levels [53].
The treatment of type 1 diabetes involves insulin injections using multiple daily injections or a pump. Insulin therapy with CGM usage leads to improvements in A1C, TIR, and TBR [60]. Currently, an algorithm-driven automated insulin delivery called hybrid closed-loop therapy is used and has shown many improvements [61,62]. Fully closed-loop automated insulin delivery systems are under development in both North America and Europe [63]. Type 1 diabetes is a disease with a large burden, so behavior modification is also important in addition to drug therapy. In this report, the importance of diabetes self-management education and support (DSMES) and psychological care are emphasized [64]. Through DSMES, psychological well-being is promoted by providing approaches, treatments, and devices that minimize the psychosocial burden of life. The overall approaches for patients with type 1 diabetes are shown in Fig. 2.
Both the 2016 and 2019 Japan Diabetes Society (JDS) clinical practice guidelines include diagnostic criteria for fulminant type 1 DM, unlike other guidelines [65]. Patients with fulminant type 1 diabetes frequently develop ketosis or ketoacidosis within 1 week of the onset of hyperglycemia, require insulin therapy immediately, and are characterized as having lower A1C values relative to their glucose values. Patients with fulminant type 1 diabetes are expected to have casual blood glucose values 288 mg/dL or higher and A1C values <8.7%, fasting C-peptide values <0.3 ng/mL, and post-glucagon load or 2-hour postprandial C-peptide values <0.5 ng/mL. Affected individuals are expected to test negative for islet autoantibodies [66].
The JDS guideline recommends that glucose-lowering agents are to be chosen in light of their pharmacological and side effect profiles to address each patient’s disease condition. There is no priority recommendation for any class of glucose-lowering agents [24]. The JDS guideline emphasizes that the pathophysiology of DM and metformin doses differ in Japanese people, whereas the results for metformin are primarily from trials in Europe and the USA [67]. They conclude that there is insufficient evidence on the effects of GLP-1 RAs and SGLT2 inhibitors on CV events in Japanese patients since there are racial and pathophysiological differences between Japanese patients and European or American patients [67]. Insulin therapy is implemented in patients with type 2 DM who have inadequate glycemic control despite medical nutrition therapy and therapy with non-insulin glucose-lowering agents, or if hyperglycemia associated glucose toxicity must be eliminated [68]. The guideline gives no cutoff value for A1C requiring insulin therapy.
Relatively detailed clinical practice guidelines for the treatment of diabetes in the elderly are presented. Elderly patients with DM are mainly characterized as (1) being susceptible to postprandial hyperglycemia and being vulnerable to hypoglycemia; (2) being susceptible to drug-related adverse effects due to factors as such impaired renal function; (3) being likely to have atherosclerotic complications; and (4) being likely to have geriatric syndromes, such as dementia, cognitive impairment, depression, decreased activities of daily living (ADL), and sarcopenia. Appropriate glycemic control focused on ensuring safety, rather than tight glycemic control, should be implemented in elderly patients with diabetes. A glycemic target of <8.5% may be allowed in patients thought to have moderate or severe dementia, impairments of ADL, or the presence of multiple comorbidities who are therefore at risk of developing adverse reactions to multi-drug combination therapy, or in those with serious comorbidities [69].
Although various guidelines present somewhat different glycemic control targets, most guidelines recommend that the glycemic control target should be individualized on the basis of patients’ clinical characteristics [1,17,65]. The threshold for initiating treatment of abnormal lipid levels and the optimal goals of low-density lipoprotein cholesterol (LDL-C) may differ according to ethnicity or population. The KDA [1] and JDS [65] guidelines recommend a somewhat less stringent LDL-C target goal in patients with type 2 DM (Table 1). The JDS guidelines recommend that the primary goal of anti-lipidemic therapy is to control the LDL-C level to <120 mg/dL in patients without a history of coronary artery disease [65]. There is no target value of LDL-C in the ADA guidelines. However, there are recommendations on the intensity of statin therapy according to the CV risk; for patients with diabetes aged 40 to 75 years without ASCVD, moderate-intensity statin therapy should be used. High-intensity statin therapy will achieve approximately a 50% reduction in LDL-C, and moderate-intensity statin regimens achieve 30% to 49% reductions in LDL-C.
Metformin remains the mainstay of the initial treatment for type 2 DM for all widely accepted recommendations and is a safe and well-tolerated treatment. The Japanese guideline does not recommend metformin as a first-line agent; instead, it recommends choosing glucose-lowering agents in light of their pharmacological and side effect profiles to address each patient’s disease condition [65]. The KDA, ADA, and AACE [17] recommend GLP-1 RAs or SGLT2 inhibitors as an appropriate initial therapy for individuals with type 2 DM with or at high-risk for ASCVD, heart failure, and/or CKD.
The KDA and AACE recommend initiating insulin in symptomatic patients with an A1C greater than 9%. The ADA recommends that the early introduction of insulin should be considered if there is evidence of ongoing catabolism (weight loss), if symptoms of hyperglycemia are present, or when A1C levels (≥10%) or blood glucose levels (≥300 mg/dL) are very high. The ADA guideline adds and highlights a new recommendation for the use of combination therapy with insulin and a GLP-1 RA for greater efficacy and durability.
Despite the tremendous amount of knowledge and advances in management tools, the quality of diabetes care still falls short of our expectations. Both standardization and individualization based on scientifically sound evidence play a key role in improving care for patients with diabetes, and practice guidelines play a critical role in guiding clinical practitioners. In this review, we summarize the most recent updates, which are also likely to be further adjusted in this rapidly changing era. It is of undoubted importance for clinicians to understand and utilize authorized guidelines as part of diabetes care, and these updates therefore need more attention.

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

Fig. 1
Treatment algorithm 1 (initial therapy) for patients with type 2 diabetes mellitus (T2DM). The algorithm stratifies the strategy of glycemic control for T2DM based on initial glycosylated hemoglobin (A1C) levels and underlying comorbidities. For newly diagnosed T2DM, begin with comprehensive lifestyle modification (LSM) at the time of diagnosis and monitor continuously. If the initial severe hyperglycemia (A1C level ≥9.0%) is accompanied by symptoms of hyperglycemia, insulin treatment should be prioritized (algorithm 3). If heart failure (HF), established atherosclerotic cardiovascular disease (eASCVD), or chronic kidney disease (CKD) are present, follow algorithm 4. If glycemic target is not achieved within 3 months after LSM, then glucose-lowering agent should be initiated promptly. If the current A1C is 1.5% higher than that of the target A1C or the current A1C level is ≥7.5%, follow algorithm 2 (combination therapy). If the A1C level is 7.5% or less, metformin monotherapy is recommended as a first-line therapy. However, if there are contraindications or intolerable side effects related to metformin use, a different class of medications can be considered. Instead of metformin monotherapy, early combination therapy could be considered to reduce the risk of failure of glycemic control in some patients with newly diagnosed T2DM. Reprinted from Hur et al. [1]. aParticularly HF with reduced ejection fraction (HFrEF, clinical diagnosis of HF and left ventricular ejection fraction ≤40%); bA history of an acute coronary syndrome or myocardial infarction, stable or unstable angina, coronary heart disease with or without revascularization, other arterial revascularization, stroke, or peripheral artery disease assumed to be atherosclerotic in origin; cestimated glomerular filtration rate <60 mL/min/1.73 m2 or urine albumin creatinine ratio ≥30 mg/g.
enm-2022-105f1.jpg
Fig. 2
A framework for the follow-up treatment of an individual with type 1 diabetes. Modified from Holt et al. [53]. CGM, continuous glucose monitoring.
enm-2022-105f2.jpg
Table 1
Comparison of Glucose, Blood Pressure, and Lipid Control Targets in Type 2 Diabetes According to Current Global Guidelines
Korean Diabetes Association (KDA) [1] Japan Diabetes Society (JDS) [65] American Diabetes Association (ADA) [35] American Association of Clinical Endocrinology (AACE) [17]
A1C, % <6.5 <6.0a <7.0 <6.5
<7.0b
<8.0c
Blood pressure, mm Hg <140/85d <130/80 <140/90f <130/80
<130/80e <130/80g
LDL-C, mg/dL <100h <120j 30%–49% <100n
<70i <100 (70)k Reductionl <70o
50% Reductionm <55p
Triglyceride, mg/dL <150 <150 - <150
HDL-C, mg/dL >40 (men) ≥40 - -
>50 (women)

A1C, glycosylated hemoglobin; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol.

a Target when aiming for normal glycemia; individuals capable of achieving glycemic control with appropriate diet or exercise therapy or those capable of achieving glycemic control while on pharmacotherapy without developing hypoglycemia;

b Target when aiming to prevent complications;

c Target when intensification of therapy considered difficult due to associated hypoglycemia or for some other reason;

d Patients with diabetes but without cardiovascular disease (CVD);

e Patients with diabetes and CVD;

f Patients with diabetes and hypertension at lower risk for CVD (10-year atherosclerotic cardiovascular disease [ASCVD] risk <15%);

g Patients with diabetes and hypertension at higher cardiovascular (CV) risk (existing ASCVD or 10-year ASCVD risk ≥15%);

h Patients with diabetes but without CVD;

i Patients with diabetes and CVD or the presence of target organ damage or CV risk factors;

j Patients without a history of coronary artery disease;

k Patients with a history of coronary artery disease; for patients who also have high-risk conditions such as familial hypercholesterolemia and diabetes complicated by other high-risk conditions (noncardiogenic cerebral infarction, peripheral artery disease, chronic kidney disease, metabolic syndrome, overlap of major risk factors, and smoking), stricter LDL-C control should be considered, with a level of <70 mg/dL as the target;

l There is no target value of LDL-C in the ADA guidelines. However, there are recommendations on the intensity of statin therapy according to the CV risk. For patients with diabetes aged 40–75 years without ASCVD, moderate-intensity statin therapy should be used. Moderate-intensity statin regimens achieve 30%–49% reductions in LDL-C;

m In patients with diabetes at higher risk, especially those with multiple ASCVD risk factors or aged 50–70 years, it is reasonable to use high-intensity statin therapy. High-intensity statin therapy will achieve approximately a 50% reduction in LDL-C;

n High-risk: DM but no other major risk and/or age <40;

o Very high risk: DM with major ASCVD risk (hypertension, family history, low HDL-C, smoking, chronic kidney disease stage 3, 4);

p Extreme risk: DM plus established CVD.

Table 2
Target Values of Continuous Glucose Monitoring Data for Most Adults with Diabetes
Variable Target value
Number of days of active CGM use 14 days preferred
Percentage of data available from active CGM use >70% of data from 14 days
Mean glucose/glucose management indicator (GMI) Individualized to targets
Glycemic variability (% CV, coefficient of variation) ≤36%
Percentage of time in range (% TIR) 70 to 180 mg/dL >70 %
Percentage of time below range (% TBR) <70 mg/dL <4 %
Percentage of time below range (% TBR) <54 mg/dL <1%
Percentage of time above range (% TAR) >180 mg/dL <25%
Percentage of time above range (%TAR) >250 mg/dL <5%

CGM, continuous glucose monitoring.

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    Figure
    • 0
    • 1
    Recent Updates to Clinical Practice Guidelines for Diabetes Mellitus
    Image Image
    Fig. 1 Treatment algorithm 1 (initial therapy) for patients with type 2 diabetes mellitus (T2DM). The algorithm stratifies the strategy of glycemic control for T2DM based on initial glycosylated hemoglobin (A1C) levels and underlying comorbidities. For newly diagnosed T2DM, begin with comprehensive lifestyle modification (LSM) at the time of diagnosis and monitor continuously. If the initial severe hyperglycemia (A1C level ≥9.0%) is accompanied by symptoms of hyperglycemia, insulin treatment should be prioritized (algorithm 3). If heart failure (HF), established atherosclerotic cardiovascular disease (eASCVD), or chronic kidney disease (CKD) are present, follow algorithm 4. If glycemic target is not achieved within 3 months after LSM, then glucose-lowering agent should be initiated promptly. If the current A1C is 1.5% higher than that of the target A1C or the current A1C level is ≥7.5%, follow algorithm 2 (combination therapy). If the A1C level is 7.5% or less, metformin monotherapy is recommended as a first-line therapy. However, if there are contraindications or intolerable side effects related to metformin use, a different class of medications can be considered. Instead of metformin monotherapy, early combination therapy could be considered to reduce the risk of failure of glycemic control in some patients with newly diagnosed T2DM. Reprinted from Hur et al. [1]. aParticularly HF with reduced ejection fraction (HFrEF, clinical diagnosis of HF and left ventricular ejection fraction ≤40%); bA history of an acute coronary syndrome or myocardial infarction, stable or unstable angina, coronary heart disease with or without revascularization, other arterial revascularization, stroke, or peripheral artery disease assumed to be atherosclerotic in origin; cestimated glomerular filtration rate <60 mL/min/1.73 m2 or urine albumin creatinine ratio ≥30 mg/g.
    Fig. 2 A framework for the follow-up treatment of an individual with type 1 diabetes. Modified from Holt et al. [53]. CGM, continuous glucose monitoring.

    Fig. 1

    Fig. 2

    Recent Updates to Clinical Practice Guidelines for Diabetes Mellitus
    Korean Diabetes Association (KDA) [1] Japan Diabetes Society (JDS) [65] American Diabetes Association (ADA) [35] American Association of Clinical Endocrinology (AACE) [17]
    A1C, % <6.5 <6.0a <7.0 <6.5
    <7.0b
    <8.0c
    Blood pressure, mm Hg <140/85d <130/80 <140/90f <130/80
    <130/80e <130/80g
    LDL-C, mg/dL <100h <120j 30%–49% <100n
    <70i <100 (70)k Reductionl <70o
    50% Reductionm <55p
    Triglyceride, mg/dL <150 <150 - <150
    HDL-C, mg/dL >40 (men) ≥40 - -
    >50 (women)
    Variable Target value
    Number of days of active CGM use 14 days preferred
    Percentage of data available from active CGM use >70% of data from 14 days
    Mean glucose/glucose management indicator (GMI) Individualized to targets
    Glycemic variability (% CV, coefficient of variation) ≤36%
    Percentage of time in range (% TIR) 70 to 180 mg/dL >70 %
    Percentage of time below range (% TBR) <70 mg/dL <4 %
    Percentage of time below range (% TBR) <54 mg/dL <1%
    Percentage of time above range (% TAR) >180 mg/dL <25%
    Percentage of time above range (%TAR) >250 mg/dL <5%
    Table 1 Comparison of Glucose, Blood Pressure, and Lipid Control Targets in Type 2 Diabetes According to Current Global Guidelines

    A1C, glycosylated hemoglobin; LDL-C, low-density lipoprotein cholesterol; HDL-C, high-density lipoprotein cholesterol.

    Target when aiming for normal glycemia; individuals capable of achieving glycemic control with appropriate diet or exercise therapy or those capable of achieving glycemic control while on pharmacotherapy without developing hypoglycemia;

    Target when aiming to prevent complications;

    Target when intensification of therapy considered difficult due to associated hypoglycemia or for some other reason;

    Patients with diabetes but without cardiovascular disease (CVD);

    Patients with diabetes and CVD;

    Patients with diabetes and hypertension at lower risk for CVD (10-year atherosclerotic cardiovascular disease [ASCVD] risk <15%);

    Patients with diabetes and hypertension at higher cardiovascular (CV) risk (existing ASCVD or 10-year ASCVD risk ≥15%);

    Patients with diabetes but without CVD;

    Patients with diabetes and CVD or the presence of target organ damage or CV risk factors;

    Patients without a history of coronary artery disease;

    Patients with a history of coronary artery disease; for patients who also have high-risk conditions such as familial hypercholesterolemia and diabetes complicated by other high-risk conditions (noncardiogenic cerebral infarction, peripheral artery disease, chronic kidney disease, metabolic syndrome, overlap of major risk factors, and smoking), stricter LDL-C control should be considered, with a level of <70 mg/dL as the target;

    There is no target value of LDL-C in the ADA guidelines. However, there are recommendations on the intensity of statin therapy according to the CV risk. For patients with diabetes aged 40–75 years without ASCVD, moderate-intensity statin therapy should be used. Moderate-intensity statin regimens achieve 30%–49% reductions in LDL-C;

    In patients with diabetes at higher risk, especially those with multiple ASCVD risk factors or aged 50–70 years, it is reasonable to use high-intensity statin therapy. High-intensity statin therapy will achieve approximately a 50% reduction in LDL-C;

    High-risk: DM but no other major risk and/or age <40;

    Very high risk: DM with major ASCVD risk (hypertension, family history, low HDL-C, smoking, chronic kidney disease stage 3, 4);

    Extreme risk: DM plus established CVD.

    Table 2 Target Values of Continuous Glucose Monitoring Data for Most Adults with Diabetes

    CGM, continuous glucose monitoring.

    Table 1

    Table 2

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