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Prediabetes and Diabetes Type 2: Screening and Making the Diagnosis

Clinical Actions:

Diabetes results when the pancreas cannot respond to or produce insulin, leading to abnormal metabolism of carbohydrates and elevated levels of glucose in the blood and urine. Type 2 diabetes (previously “noninsulin-dependent diabetes” or “adult-onset diabetes”) accounts for 90–95% of all diabetes. Type 2 diabetes is caused by a progressive loss of β-cell insulin secretion, usually associated with insulin resistance. Prediabetes is diagnosed when glucose levels start to rise due to β-cell insulin secretion failure, but diagnostic criteria are not yet met for Type 2 diabetes.

Table of Contents  

Evaluate Patients for Risk Factors

Risk Factors for Type 2 Diabetes (NIDDK)

  • Overweight or obese
    • NIDDK BMI chart (see ‘Primary Sources – Learn More’ below)
      • Not Asian American or Pacific Islander: At-risk BMI ≥ 25
      • Asian American: At-risk BMI ≥ 23
      • Pacific Islander: At-risk BMI ≥ 26
  • ≥45 years
  • Family history of diabetes
  • Race/Ethnicity
    • African American, Alaska Native, American Indian, Asian American, Hispanic/Latino, Native Hawaiian, or Pacific Islander
  • Hypertension (or on therapy for hypertension)
  • Dyslipidemia
  • Personal history of
    • Pregnancy: GDM or macrosomia (BW >4000 g)
    • Physical inactivity
    • Heart disease or stroke
    • Depression
    • PCOS
    • Acanthosis nigricans
    • HIV

Screening and Diagnostic Criteria

Who and When to Screen


  • Overweight or obesity (BMI ≥25 kg/m2 or ≥23 kg/m2 in Asian Americans) and ≥1 of the following risk factors
    • First-degree relative with diabetes
    • High-risk race/ethnicity (e.g., African American, Latino, Native American, Asian American, Pacific Islander)
    • History of CVD
    • Hypertension (≥140/90 mmHg or on therapy for hypertension)
    • HDL cholesterol level <35 mg/dL (0.90 mmol/L) and/or a triglyceride level >250 mg/dL (2.82 mmol/L)
    • Women with polycystic ovary syndrome
    • Physical inactivity
    • Other clinical conditions associated with insulin resistance (e.g., severe obesity, acanthosis nigricans)
  • People with HIV
    • Screen for diabetes and prediabetes with a fasting glucose test
      • Before starting antiretroviral therapy
      • At the time of switching antiretroviral therapy
      • 3 to 6 months after starting or switching antiretroviral therapy
    • If initial screening results are normal, fasting glucose should be checked annually
  • Patients with prediabetes (A1C ≥5.7% [39 mmol/mol], IGT, or IFG) should be tested yearly
  • Women who were diagnosed with GDM should have lifelong testing at least every 3 years
  • For all other patients, testing should begin at age 35 years
  • If results are normal, testing should be repeated at a minimum of 3-year intervals, with consideration of more frequent testing depending on initial results and risk status


  • Begin at age 45 without risk factors
  • Screening based on risk factors: In addition to the above list, AACE/ACE includes the following factors
    • Antipsychotic therapy for schizophrenia and/or severe bipolar disease
    • Chronic glucocorticoid exposure
    • Sleep disorders (e.g., obstructive sleep apnea, chronic sleep deprivation, and night shift occupation) with glucose intolerance
  • Normal glucose values: Every 3 years
  • Consider annual screening for patients with 2 or more risk factors


  • Screen for prediabetes and type 2 diabetes in adults aged 35 to 70 years who have overweight (BMI ≥25) or obesity (BMI ≥30)
  • Clinicians should offer or refer patients with prediabetes to effective preventive interventions
  • Above are Grade B recommendations: Offer or provide this service

Diagnostic Criteria

  • Normal
    • Fasting plasma glucose (FPG) <100 mg/dL (5.6 mmol per L)
    • Oral glucose tolerance test (OGTT) with 75g glucose load
      • 2h (plasma glucose) PG <140 mg/dL (7.8 mmol per L)
  • High Risk for Diabetes (prediabetes)
    • Impaired fasting glucose (IFG): FPG ≥100 to 125 mg/dL (5.6 to 6.9 mmol per L)
    • Impaired glucose tolerance (IGT): 2h PG ≥140 to 199 mg/dL (7.8 to 11.0 mmol per L)
    • A1C 5.7% to 6.4%
    • Note: Patients with prediabetes should be tested yearly
  • Diabetes: Glucose criteria are preferred for the diagnosis of DM
    • FPG ≥126 (7.0 mmol per L) mg/dL
    • OGTT: 2h PG ≥200 mg/dL (11.1 mmol per L)
    • Random PG ≥200 mg/dL (11.1 mmol per L) with the following symptoms of hyperglycemia
      • Polydipsia | Polyuria | Polyphagia | Blurred vision | Weakness | Unexplained weight loss
    • A1C ≥6.5%
    • Note: Always confirm diabetes diagnosis with repeat glucose or A1C testing on another day


Prediabetes is not a clinical disorder but rather an important risk factor for diabetes and cardiovascular disease. While there are some differences between organizations regarding risk factors for screening and diagnostic cut-offs, all agree as to the importance of identifying those at risk for significant cardiovascular events if diabetes is left untreated. The prognosis for type 2 diabetes varies and is very dependent on glucose control.


Symptoms of Diabetes (related to hyperglycemia)

  • Excessive urination, thirst and hunger 
  • Unexpected weight loss 
  • Increased susceptibility to infections, especially yeast or fungal infections 
  • Weak, tired feeling
  • Dry mouth
  • Blurry vision
  • Deposits of blood, or puffy yellow spots in the retina
  • Decreased sensation in the legs
  • Weak pulses in the feet
  • Blisters, ulcers or infections of the feet 

Complications of Type 2 Diabetes

  • Atherosclerosis
  • Retinopathy 
  • Neuropathy 
  • Nephropathy
  • Dermatologic pathology
    • Infections
    • Feet in particular: Ulcerations with poor healing  

Learn More – Primary Sources:

ADA: Classification and Diagnosis of Diabetes: Standards of Medical Care in Diabetes—2022

AACE/ACE Clinical Practice Guidelines for Developing a Diabetes Mellitus Comprehensive Care Plan

Consensus Statement By The American Association Of Clinical Endocrinologists And American College Of Endocrinology On The Comprehensive Type 2 Diabetes Management Algorithm – 2020 Executive Summary

NIDDK: Risk Factors for Type 2 Diabetes

USPSTF: Screening for Prediabetes and Type 2 Diabetes

HIV and Diabetes | NIH

Treating Type 2 Diabetes


  • Treatment of Type 2 Diabetes, whether new onset or persistent, requires multimodal, comprehensive management. Diabetic treatment includes lifestyle changes, weight management, and pharmacologic approaches. Aside from antihyperglycemic agents, patients may also require lipid-lowering and antihypertensive medications
  • Initial therapy and A1C
  • Lifestyle therapy plus antihyperglycemic monotherapy (preferably with metformin)
  • A1C target (See ‘Related ObG Topic’ below): Currently, there are different professional guideline thresholds
    • ACP: Aim to achieve an HbA1c level between 7% and 8% in most patients with type 2 diabetes and consider deintensifying pharmacologic therapy in patients with type 2 diabetes who achieve HbA1c levels less than 6.5%
    • ADA: Recommends <7% for the general population and to consider more stringent goals (<6.5%) for selected patients without significant hypoglycemia (e.g., long life expectancy, no CVD and treated with lifestyle or metformin only)
    • AACE/ACE: ≤6.5% if target can be achieved safely
  • ADA Treatment Recommendations Include the Following

    • Metformin is the preferred initial medication if tolerated by patient, with other agents added to metformin as needed to achieve target
      • Benefits: Low hypoglycemia risk | May help with modest weight loss | Good antihyperglycemic efficacy at doses of 1,000 to 2,000 mg/day
      • Side effects: GI intolerance (bloating, abdominal discomfort, and diarrhea)
      • Renal disease: Can be used with reduced estimated glomerular filtration rates (eGFR) ≥30 mL/min/1.73 m2
      • Vitamin B12 deficiency: Periodically test for vitamin B12 levels
    • Consider early introduction of insulin
      • Catabolism: Weight loss | Hypertriglyceridemia | Ketosis
      • Hyperglycemic symptoms
      • A1C levels >10% (86 mmol/mol) or blood glucose levels ≥300 mg/dL (16.7 mmol/L)
    • Dual therapy: Consider in newly diagnosed patients if A1C ≥1.5% (12.5 mmol/mol) above target
      • Initial dual therapy extends time to treatment failure (compared to sequential addition of medications)
      • High costs and tolerability issues are important barriers to the use of GLP-1 receptor agonists
    • Continue metformin for as long as tolerated and not contraindicated
      • Add other agents, including insulin, to metformin
      • Glucagon-like peptide 1 receptor agonist is preferred to insulin when possible

    With Comorbidities in addition to Type 2 Diabetes

    • In patients with known atherosclerotic cardiovascular disease or at high risk, kidney disease, or heart failure, the following are recommended
      • Sodium–glucose cotransporter 2 inhibitors
      • Glucagon-like peptide 1 receptor agonists with demonstrated CVD benefit
    • Consideration of these medications in the setting of these co-morbidities is independent of HbA1C or HbA1C target


    Management should be individualized based on numerous factors, such as age, life expectancy, comorbid conditions, duration of diabetes, risk of hypoglycemia or adverse consequences from hypoglycemia, patient motivation, and adherence. The ADA states that

    A patient-centered approach should be used to guide the choice of pharmacologic agents. Considerations include comorbidities (atherosclerotic cardiovascular disease, heart failure, chronic kidney disease), hypoglycemia risk, impact on weight, cost, risk for side effects, and patient preferences.


    Lifestyle Modification

    • ACCE/ACE list the following as key areas for lifestyle modification
      • Nutrition: Weight management | plant-based diet
      • Physical Activity: 150 min/week exertion such as walking or stair climbing | Strength training
      • Sleep: About 6 to 8 hours/night
      • Behavioral support: Community engagement | Alcohol moderation
      • Smoking cessation: No tobacco products


    Noninsulin Glucose-Lowering Agents

    • Biguanides
      • Metformin is considered first line medication
      • Acceptable alternatives (described below) to metformin as initial therapy include
        • GLP1 receptor agonists | SGLT2 inhibitors | DPP4 inhibitors | TZDs | AGIs
        • SUs, and glinides may also be appropriate as monotherapy for select patients
    • GLP1 receptor agonists (GLP-RA): Exenatide | Dulaglutide | Semaglutide | Liraglutide
      • Next in line to be added to metformin when dual or triple therapy indicated (same suggested hierarchy level as SGLT2i)
      • Strong A1C-lowering properties: Associated with decreased weight, lipid and BP
    • Sodium-glucose cotransporter 2 inhibitors (SGLT2i): Ertugliflozin | Dapagliflozin | Canagliflozin | Empagliflozin
      • Next in line to be added to metformin when dual or triple therapy indicated (same suggested hierarchy level as GLP1-RA)
      • Glucosuric effect: Associated with decreased A1C, weight, and systolic BP
    • Dipeptidyl peptidase 4 inhibitors (DPP4i): Alogliptin | Saxagliptin | Linagliptin | Sitagliptin
      • Inhibit DPP4 and increase GLP1 and other incretin hormones | Modestly lower A1C | low risk of hypoglycemia
      • Combination pills available with metformin, SGLT2 inhibitors, and a TZD
    • Thiazolidinediones (TZDs): Pioglitazone | Rosiglitazone
      • Directly reduce insulin resistance | Potent A1C-lowering properties | Low risk of hypoglycemia
      • Caution recommended due to associated risk factors: Weight gain | Increased bone fracture risk in postmenopausal females and elderly males | Elevated risk for chronic edema or heart failure
    • Alpha-glucosidase inhibitors (AGIs): Acarbose | Miglitol
      • Modest A1C-lowering effects | Low hypoglycemia risk
      • Limited use in the US
    • Insulin-secretagogues
      • Sulfonylureas (SUs): Glimepiride | Glipizide | Glyburide
        • Relatively potent A1C-lowering effects
        • Effects may not last | May increase weight | Risk for hypoglycemia and CVD
      • Glinides: Nateglinide | Repaglinide
        • Shorter half-life than SUs, with lower A1C-lowering effects but also lower risk of prolonged hypoglycemia
    • Other medications
      • Bromocriptine | Colsevelam (bile acid sequestrant)

    Note: While the ACE/ACCE algorithm (see below in ‘Learn More – Primary Sources) places GLP-RA and SGLT2i drugs as next in line to combine with metformin, the ADA states

    If the A1C target is not achieved after approximately 3 months, metformin can be combined with any one of the preferred six treatment options: sulfonylurea, thiazolidinedione, DPP-4 inhibitor, SGLT2 inhibitor, GLP-1 RA, or basal insulin; the choice of which agent to add is based on drug-specific effects and patient factors


    • Most potent antihyperglycemic agent
    • Considerations prior to use
      • Patient motivation | CVD, comorbidities and complications | Age | Risk for Hypoglycemia | Overall health |Cost considerations
    • Basal analogs: Glargine | Detemir | Degludec
      • Flat serum insulin concentration for 24 hours or longer
    • Human Neutral protamine Hagedorn (NPH) insulin
      • More likely to cause hypoglycemia than basal analogs
    • Addition of human NPH or long-acting insulin analogs to oral agents is “well-established approach that is effective for many patients” (ADA)
    • Rapid acting Insulin: Glulisine | Lispro | Aspart | Inhaled insulin (preferable to regular human)
      • May be necessary at mealtime if glycemia uncontrolled despite combination of oral medications and insulin/GLP1-RA
    • Premixed insulins combining longer and shorter action insulin available but less flexible and greater risk of hypoglycemia

    Management Summary (Initiation)

    • Recent onset T2D and A1C
    • Monotherapy (preferably metformin)
  • A1C >7.5% (whether newly diagnosed or not)
    • If not already taking antihyperglycemic agents start on metformin plus another agent
  • A1C >9.0%
    • Symptomatic (polyuria, polydipsia, or polyphagia): Will likely need insulin
    • Asymptomatic: Start with 2 or 3 non-insulin medications
  • Note: Link to detailed ACE/ACCE Glycemic Control algorithm available in ‘Learn More – Primary Sources’ below)

    Self-Monitoring of Blood Glucose (SMBG)

    • Recommended for patients on intensive insulin therapy (basal plus prandial insulin)
      • Check prior to meals/snacks, prior to exercise, and at bedtime
      • Once-daily fasting glucose in patient on basal insulin only
      • Limited benefit for patients on oral therapy only
    • Continuous glucose monitoring (CGM) devices are emerging as a complement to SMBG
      • Strong correlation between “time in range” (TIR) and HbA1c (70% TIR equates to HbA1c ~7%)
    • Patients not on insulin
      • Routine glucose monitoring likely limited in clinical value
      • For some, may provide insight regarding exercise, diet and medication management


    • Risk for antihyperglycemic agents, especially insulin
    • Some classes have lower risk for hypoglycemia
      • Metformin | GLP1 receptor agonists | SGLT2 inhibitors | DPP4 inhibitors | TZDs
      • However, hypoglycemia can still occur in combination with an insulin secretagogue or exogenous insulin
    • Screen patients for evidence of hypoglycemia unawareness
      • Young children with type I diabetes and elderly are particularly vulnerable
      • Interventions include: Medication or diet adjustments | Patient education | Individualized glycemic goals
    • Educate patients regarding symptoms
      • Tremors or feeling shaky | Nervous or anxious | Sweating, chills and clamminess | Irritability | Confusion | Tachycardia | Lightheaded or dizziness | Pallor | Drowsy or weakness | Blurred/impaired vision | Tingling or numbness in the lips, tongue, or cheeks | Headaches | Lack of coordination | Seizures (severe)
    • “15-15 Rule”: Raise glucose to >70 mg/dL with 15 grams carbohydrate intake and check glucose at 15 minutes | Repeat if glucose still
    • Glucose tablets or gel tube | 4 ounces (1/2 cup) of juice or regular (non-diet) soda | 1 tablespoon of sugar, honey, or corn syrup | Hard candies, jellybeans, or gumdrops (based on labelling)
  • Severe hypoglycemia (patient cannot treat herself or unconscious): Glucagon
    • Available by injection (buttock, arm or thigh) or nasal powder (does not require inhalation)
  • Additional Notes

    • GLP1-RA is preferable to insulin for those patients who may require an injectable medication
    • Patients who require a 3rd medication and who have A1C >8.0% and/or long-standing disease: Less likely to reach their target A1C with a third oral antihyperglycemic agent
      • While adding GLP1-RA may initially work, many patients will still require insulin
    • Reevaluate medications regularly
      • Every 3 to 6 months
      • Adjust as needed based on new patient factors
      • Yearly visits (or more frequent depending on clinical findings) to ophthalmologist and podiatrist
    • Important to prevent complications and slow CVD / renal disease
      • Manage risk factors for atherosclerosis (e.g., BP, cholesterol, smoking, obesity)

    Learn More – Primary Sources

    FDA List of Approved Diabetes Medications

    AACE/ACE Comprehensive Type 2 Diabetes Management Algorithm

    ADA Pharmacologic Approaches to Glycemic Treatment: Standards of Medical Care in Diabetes—2022

    Hemoglobin A1c Targets for Glycemic Control With Pharmacologic Therapy for Nonpregnant Adults With Type 2 Diabetes Mellitus: A Guidance Statement Update From the American College of Physicians

    CDC-Recognized Lifestyle Change Program

    ADA Healthcare Professional Resources