| Literature DB >> 26807004 |
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Abstract
Entities:
Year: 2016 PMID: 26807004 PMCID: PMC4714725 DOI: 10.2337/diaclin.34.1.3
Source DB: PubMed Journal: Clin Diabetes ISSN: 0891-8929
Criteria for the Diagnosis of Diabetes
| FPG ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8 h. |
| OR |
| 2-h plasma glucose ≥200 mg/dL (11.1 mmol/L) during an OGTT. The test should be performed as described by the World Health Organization, using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water. |
| OR |
| A1C ≥6.5% (48 mmol/mol). The test should be performed in a laboratory using a method that is NGSP certified and standardized to the DCCT assay. |
| OR |
| In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose ≥200 mg/dL (11.1 mmol/L). |
In the absence of unequivocal hyperglycemia, results should be confirmed by repeat testing.
Only diagnostic in a patient with classic symptoms of hyperglycemia or hyperglycemic crisis.
Criteria for Testing for Diabetes or Prediabetes in Asymptomatic Adults
| 1. Testing should be considered in all adults who are overweight (BMI ≥25 kg/m2 or ≥23 kg/m2 in Asian Americans) and have additional risk factors: Physical inactivity First-degree relative with diabetes High-risk race/ethnicity (e.g., African American, Latino, Native American, Asian American, Pacific Islander) Women who delivered a baby weighing >9 lb or were diagnosed with GDM 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 A1C ≥5.7% (39 mmol/mol), IGT, or IFG on previous testing Other clinical conditions associated with insulin resistance (e.g., severe obesity, acanthosis nigricans) History of CVD |
| 2. For all patients, testing should begin at age 45 years. |
| 3. 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 (e.g., those with prediabetes should be tested yearly) and risk status. |
IFG, impaired fasting glucose; IGT, impaired glucose tolerance.
Testing for Type 2 Diabetes or Prediabetes in Asymptomatic Children*
Overweight (BMI >85th percentile for age and sex, weight for height >85th percentile, or weight >120% of ideal for height) |
Family history of type 2 diabetes in first- or second-degree relative Race/ethnicity (Native American, African American, Latino, Asian American, Pacific Islander) Signs of insulin resistance or conditions associated with insulin resistance (acanthosis nigricans, hypertension, dyslipidemia, polycystic ovary syndrome, or small-for-gestational-age birth weight) Maternal history of diabetes or GDM during the child’s gestation |
People aged ≤18 years.
Components of the Comprehensive Diabetes Medical Evaluation
| • Age and characteristics of onset of diabetes (e.g., DKA, asymptomatic laboratory finding) |
| • Eating patterns, nutritional status, weight history, and physical activity habits; nutrition education and behavioral support history and needs |
| • Presence of common comorbidities, psychosocial problems, and dental disease |
| • Screen for depression using PHQ-2 (PHQ-9 if PHQ-2 positive) or EPDS |
| • Screen for DD using DDS or PAID-1 |
| • History of smoking, alcohol consumption, and substance use |
| • Diabetes education, self-management, and support history and needs |
| • Review of previous treatment regimens and response to therapy (A1C records) |
| • Results of glucose monitoring and patient’s use of data |
| • DKA frequency, severity, and cause |
| • Hypoglycemia episodes, awareness, and frequency and causes |
| • History of increased blood pressure, increased lipids, and tobacco use |
| • Microvascular complications: retinopathy, nephropathy, and neuropathy (sensory, including history of foot lesions; autonomic, including sexual dysfunction and gastroparesis) |
| • Macrovascular complications: coronary heart disease, cerebrovascular disease, and peripheral arterial disease |
| • Height, weight, and BMI; growth and pubertal development in children and adolescents |
| •Blood pressure determination, including orthostatic measurements when indicated |
| •Fundoscopic examination |
| •Thyroid palpation |
| •Skin examination (e.g., for acanthosis nigricans, insulin injection, or infusion set insertion sites) |
| •Comprehensive foot examination |
| ○ Inspection |
| ○ Palpation of dorsalis pedis and posterior tibial pulses |
| ○ Presence/absence of patellar and Achilles reflexes |
| ○ Determination of proprioception, vibration, and monofilament sensation |
| •A1C, if results not available within the past 3 months |
| •If not performed/available within the past year |
| ○ Fasting lipid profile, including total, LDL, and HDL cholesterol and triglycerides, as needed |
| ○ Liver function tests |
| ○ Spot urinary albumin–to–creatinine ratio |
| ○ Serum creatinine and estimated glomerular filtration rate |
| ○ Thyroid-stimulating hormone in patients with type 1 diabetes or dyslipidemia or women aged >50 years |
DD, diabetes distress; DDS, Diabetes Distress Scale; DKA, diabetic ketoacidosis; EPDS, Edinburgh Postnatal Depression Scale; PAID, Problem Areas in Diabetes; PHQ, Patient Health Questionnaire.
Nutrition Therapy Recommendations
| Topic | Recommendations | Evidence rating |
| Effectiveness of nutrition therapy | An individualized MNT program, preferably provided by a registered dietitian, is recommended for all people with type 1 or type 2 diabetes. | |
For people with type 1 diabetes or those with type 2 diabetes who are prescribed a flexible insulin therapy program, education on how to use carbohydrate counting or estimation to determine mealtime insulin dosing can improve glycemic control. | ||
For individuals whose daily insulin dosing is fixed, having a consistent pattern of carbohydrate intake with respect to time and amount can result in improved glycemic control and a reduced risk of hypoglycemia. | ||
A simple and effective approach to glycemia and weight management emphasizing healthy food choices and portion control may be more helpful for those with type 2 diabetes who are not taking insulin, who have limited health literacy or numeracy, and who are elderly and prone to hypoglycemia. | ||
Because diabetes nutrition therapy can result in cost savings | ||
| Energy balance | Modest weight loss achievable by the combination of lifestyle modification and the reduction of energy intake benefits overweight or obese adults with type 2 diabetes and also those at risk for diabetes. Interventional programs to facilitate this process are recommended. | |
| Eating patterns and macronutrient distribution | As there is no single ideal dietary distribution of calories among carbohydrates, fats, and proteins for people with diabetes, macronutrient distribution should be individualized while keeping total calorie and metabolic goals in mind. | |
Carbohydrate intake from whole grains, vegetables, fruits, legumes, and dairy products, with an emphasis on foods higher in fiber and lower in glycemic load, should be advised over other sources, especially those containing sugars. | ||
People with diabetes and those at risk should avoid sugar-sweetened beverages in order to control weight and reduce their risk for CVD and fatty liver | ||
| Protein | In individuals with type 2 diabetes, ingested protein appears to increase insulin response without increasing plasma glucose concentrations. Therefore, carbohydrate sources high in protein should not be used to treat or prevent hypoglycemia. | |
| Dietary fat | Whereas data on the ideal total dietary fat content for people with diabetes are inconclusive, an eating plan emphasizing elements of a Mediterranean-style diet rich in monounsaturated fats may improve glucose metabolism and lower CVD risk and can be an effective alternative to a diet low in total fat but relatively high in carbohydrates. | |
Eating foods rich in long-chain omega-3 fatty acids, such as fatty fish (EPA and DHA) and nuts and seeds (ALA), is recommended to prevent or treat CVD | ||
| Micronutrients and herbal supplements | There is no clear evidence that dietary supplementation with vitamins, minerals, herbs, or spices can improve diabetes, and there may be safety concerns regarding the long-term use of antioxidant supplements such as vitamins E and C and carotene. | |
| Alcohol | Adults with diabetes who drink alcohol should do so in moderation (no more than one drink per day for adult women and no more than two drinks per day for adult men). | |
Alcohol consumption may place people with diabetes at increased risk for delayed hypoglycemia, especially if taking insulin or insulin secretagogues. Education and awareness regarding the recognition and management of delayed hypoglycemia are warranted. | ||
| Sodium | As for the general population, people with diabetes should limit sodium consumption to ≤2,300 mg/day, although further restriction may be indicated for those with both diabetes and hypertension. |
FIGURE 1.Depicted are patient and disease factors used to determine optimal A1C targets. Characteristics and predicaments toward the left justify more stringent efforts to lower A1C; those toward the right suggest less stringent efforts. Adapted with permission from Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in type 2 diabetes, 2015: a patient-centered approach: update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care 2015;38:140–149.
Summary of Glycemic Recommendations for Nonpregnant Adults With Diabetes
| A1C | <7.0% (53 mmol/mol) |
| Preprandial capillary plasma glucose | 80–130 mg/dL |
| Peak postprandial capillary plasma glucose | <180 mg/dL |
More or less stringent glycemic goals may be appropriate for individual patients. Goals should be individualized based on duration of diabetes, age/life expectancy, comorbid conditions, known CVD or advanced microvascular complications, hypoglycemia unawareness, and individual patient considerations.
Postprandial glucose may be targeted if A1C goals are not met despite reaching preprandial glucose goals. Postprandial glucose measurements should be made 1–2 hours after the beginning of the meal, generally peak levels in patients with diabetes.
FIGURE 2.Antihyperglycemic therapy in type 2 diabetes: general recommendations. The order in the chart was determined by historical availability and the route of administration, with injectables to the right; it is not meant to denote any specific preference. Potential sequences of antihyperglycemic therapy for patients with type 2 diabetes are displayed, with the usual transition moving vertically from top to bottom (although horizontal movement within therapy stages is also possible, depending on the circumstances). DPP-4-i, DPP-4 inhibitor; fxs, fractures; GI, gastrointestinal; GLP-1-RA, GLP-1 receptor agonist; GU, genitourinary; HF, heart failure; Hypo, hypoglycemia; SGLT2-i, SGLT2 inhibitor; SU, sulfonylurea; TZD, thiazolidinedione. *See ref. 17 in the full SOC document for description of efficacy categorization. †Consider starting at this stage when A1C is ≥9% (75 mmol/mol). ‡Consider starting at this stage when blood glucose is ≥300–350 mg/dL (16.7–19.4 mmol/L) and/or A1C is ≥10–12% (86–108 mmol/mol), especially if symptomatic or catabolic features are present, in which case basal insulin + mealtime insulin is the preferred initial regimen. §Usually a basal insulin (NPH, glargine, detemir, degludec). Adapted with permission from Inzucchi SE, Bergenstal RM, Buse JB, et al. Management of hyperglycemia in type 2 diabetes, 2015: a patient-centered approach: update to a position statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care 2015;38:140–149.
Recommendations for Statin and Combination Treatment in People With Diabetes
| Age | Risk factors | Recommended statin intensity |
| <40 years | None | None |
| ASCVD risk factor(s) | Moderate or high | |
| ASCVD | High | |
| 40–75 years | None | Moderate |
| ASCVD risk factors | High | |
| ASCVD | High | |
| ACS and LDL cholesterol >50 mg/dL (1.3 mmol/L) in patients who cannot tolerate high-dose statins | Moderate plus ezetimibe | |
| >75 years | None | Moderate |
| ASCVD risk factors | Moderate or high | |
| ASCVD | High | |
| ACS and LDL cholesterol >50 mg/dL (1.3 mmol/L) in patients who cannot tolerate high-dose statins | Moderate plus ezetimibe |
In addition to lifestyle therapy.
ASCVD risk factors include LDL cholesterol ≥100 mg/dL (2.6 mmol/L), high blood pressure, smoking, overweight and obesity, and family history of premature ASCVD. ACS, acute coronary syndrome.
High- and Moderate-Intensity Statin Therapy*
| High-intensity statin therapy | Moderate-intensity statin therapy |
| Lowers LDL cholesterol by ≥50% | Lowers LDL cholesterol by 30% to <50% |
| Atorvastatin 40–80 mg | Atorvastatin 10–20 mg |
| Rosuvastatin 20–40 mg | Rosuvastatin 5–10 mg |
| Simvastatin 20–40 mg | |
| Pravastatin 40–80 mg | |
| Lovastatin 40 mg | |
| Fluvastatin XL 80 mg | |
| Pitavastatin 2–4 mg |
Once-daily dosing.
Management of CKD in Diabetes
| GFR (mL/min/1.73 m2) | Recommended management |
| All patients | Yearly measurement of creatinine, UACR, potassium |
| 45–60 | Referral to a nephrologist if possibility for nondiabetic kidney disease exists (duration of type 1 diabetes <10 years, persistent albuminuria, abnormal findings on renal ultrasound, resistant hypertension, rapid fall in eGFR, or active urinary sediment on urine microscopic examination) |
| Consider the need for dose adjustment of medications | |
| Monitor eGFR every 6 months | |
| Monitor electrolytes, bicarbonate, hemoglobin, calcium, phosphorus, and parathyroid hormone at least yearly | |
| Assure vitamin D sufficiency | |
| Consider bone density testing | |
| Referral for dietary counseling | |
| 30–44 | Monitor eGFR every 3 months |
| Monitor electrolytes, bicarbonate, calcium, phosphorus, parathyroid hormone, hemoglobin, albumin, and weight every 3–6 months | |
| Consider the need for dose adjustment of medications | |
| <30 | Referral to a nephrologist |
Framework for Considering Treatment Goals for Glycemia, Blood Pressure, and Dyslipidemia in Older Adults With Diabetes
| Patient characteristics/health status | Rationale | Reasonable A1C goal | Fasting or preprandial glucose | Bedtime glucose | Blood pressure (mmHg) | Lipids | ||
| mg/dL | mmol/L | mg/dL | mmol/L | |||||
| Healthy (few coexisting chronic illnesses, intact cognitive and functional status) | Longer remaining life expectancy | <7.5% (58 mmol/mol) | 90–130 | 5.0–7.2 | 90–150 | 5.0–8.3 | <140/90 | Statin unless contraindicated or not tolerated |
| Complex/intermediate (multiple coexisting chronic illnesses | Intermediate remaining life expectancy, high treatment burden, hypoglycemia vulnerability, fall risk | <8.0% (64 mmol/mol) | 90–150 | 5.0–8.3 | 100–180 | 5.6–10.0 | <140/90 | Statin unless contraindicated or not tolerated |
| Very complex/poor health (LTC or end-stage chronic illnesses | Limited remaining life expectancy makes benefit uncertain | <8.5% | 100–180 | 5.6–10.0 | 110–200 | 6.1–11.1 | <150/90 | Consider likelihood of benefit with statin (secondary prevention more so than primary) |
This represents a consensus framework for considering treatment goals for glycemia, blood pressure, and dyslipidemia in older adults with diabetes. The patient characteristic categories are general concepts. Not every patient will clearly fall into a particular category. Consideration of patient and caregiver preferences is an important aspect of treatment individualization. Additionally, a patient’s health status and preferences may change over time. ADL, activities of daily living.
A lower A1C goal may be set for an individual if achievable without recurrent or severe hypoglycemia or undue treatment burden.
Coexisting chronic illnesses are conditions serious enough to require medications or lifestyle management and may include arthritis, cancer, congestive heart failure, depression, emphysema, falls, hypertension, incontinence, stage 3 or worse chronic kidney disease, myocardial infarction, and stroke. By “multiple,” we mean at least three, but many patients may have five or more.
The presence of a single end-stage chronic illness, such as stage 3–4 congestive heart failure or oxygen-dependent lung disease, chronic kidney disease requiring dialysis, or uncontrolled metastatic cancer, may cause significant symptoms or impairment of functional status and significantly reduce life expectancy.
A1C of 8.5% (69 mmol/mol) equates to an estimated average glucose of ∼200 mg/dL (11.1 mmol/L). Looser A1C targets above 8.5% (69 mmol/mol) are not recommended as they may expose patients to more frequent higher glucose values and the acute risks from glycosuria, dehydration, hyperglycemic hyperosmolar syndrome, and poor wound healing.