il diabete di tipo 2 emanuele bosi corso di endocrinologia e malattie del ricambio università...
TRANSCRIPT
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Il Diabete di Tipo 2
Emanuele Bosi
Corso di Endocrinologia e Malattie del Ricambio
Università Vita-Salute San Raffaele A.A. 2009-2010
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Il Diabete Mellito di tipo 2• Forma di diabete ad esordio prevalentemente adulto, caratterizzata
da insulino-resistenza ed insulino deficienza relativa.
• Normalmente non richiede terapia insulinica
• Eziologia ignota:
- forte componente genetica (concordanza gemelli identici >90%) a localizzazione sconosciuta.
- fattori di rischio: sovrappeso e obesità, sedentarietà, età, ipertensione arteriosa, dislipidemia
• Fenotipo fisiopatologico relativamente eterogeneo
• Non evolve mai in chetoacidosi; in casi estremi coma iperosmolare
• Per molti anni può decorrere in modo totalmente asintomatico
• Si associa ad un aumentato rischio di morbosità e mortalità cardiovascolare anche per livelli glicemici modestamente elevati
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Quanto è diffuso
il diabete di tipo 2?
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The type 2 diabetes pandemia
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Adapted from WHO Diabetes Programme Facts and Figures: www.who.int/diabetes/facts/world_figures/en. Accessed 1 August, 2006.
Worldwide prevalence of diabetes in 2000
Number of persons
< 5,0005,000–74,00075,000–349,000350,000–1,499,0001,500,000–4,999,000> 5,000,000No data available
Total cases 150 million adults
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Worldwide prevalence of diabetes in 2030 (projected)
Total cases > 300 million adults
Number of persons
< 5,0005,000–74,00075,000–349,000350,000–1,499,0001,500,000–4,999,000> 5,000,000No data available Adapted from WHO Diabetes Programme Facts and Figures:
www.who.int/diabetes/facts/world_figures/en. Accessed 1 August, 2006.
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Prevalenza delle alterazioni del metabolismo dei carboidrati in Italia
età come fattore di rischio
Diabete di tipo 2 IGT
Anni % %45-54 5.2 4.455-64 11.3 6.665-74 15.1 10.3>75 16.6 19.4>45 anni 11.1 8.2
- noto 8.2 -- non-noto 2.9 -
Cremona Study
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Pathophysiology and Natural History of Type 2 Diabetes
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Abnormal Islet Function Determines the Development of IGT and T2DM in the Setting of Insulin Resistance
Genetics, age, lifestyle, environmental factors
Insulin resistance
Normal islet function
NGT IGT / T2DM
Abnormal islet function
T2DM = type 2 diabetes mellitus; NGT = normal glucose tolerance; IGT = impaired glucose tolerance
Adapted from Ahren B, Pacini G. Diabetes Obes Metab. 2005;7(1):2–8.
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Adapted from International Diabetes Center. Type 2 Diabetes BASICS. Minneapolis, MN:International Diabetes Center; 2000.
Prediabetes(IFG/IGT)
NGT Diabetes
Diagnosis
Natural history of type 2 diabetes: progressive deterioration of Islet Cell Function
in the Setting of Insulin Resistance
Insulin Resistance
Islet Dysfunction
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Insulino resistenza
Definizione: Ridotto effetto biologico dell’insulina per difetto a localizzazione post-recettoriale
Eziologia: indeterminataFattori di rischio:• Genetici: elevata familiarità, geni non identificati• Età• Sedentarietà• Alimentazione• Obesità e sovrappeso
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INSULIN
RESISTANCELiver, muscle, adipocyte
endothelium
Obesity
DyslipidemiaHypertension
Type 2diabetes
Insulin resistance is a common feature of many human diseases
Cardiovascular disease
Polycystic ovarysyndrome (PCOS)
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Obesità come fattore di rischio per diabete di tipo 2Obesità come fattore di rischio per diabete di tipo 2
Carey et al., Carey et al., Am J Epidemiol,Am J Epidemiol, 1997 1997
Ris
chio
Rel
ativ
oR
isch
io R
elat
ivo
71–75.971–75.9
2424
2020
1616
1212
88
44
00<71<71 76–8176–81 81.1–8681.1–86 86.1–9186.1–91 91.1–96.391.1–96.3 96.496.4
Circonferenza addominale (cm)Circonferenza addominale (cm)
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Years from diagnosisYears from diagnosis
-Cell Function Declines While Insulin Sensitivity Remains Stable in Type -Cell Function Declines While Insulin Sensitivity Remains Stable in Type
2 Diabetes2 Diabetes
10-year follow-up of the Belfast Diet Study: Data from 67 newly diagnosed subjects with type 2 diabetes mellitus (N=432) who 10-year follow-up of the Belfast Diet Study: Data from 67 newly diagnosed subjects with type 2 diabetes mellitus (N=432) who required oral antihyperglycemic therapy or insulin due to secondary failure of diet therapy at 5–7 years.required oral antihyperglycemic therapy or insulin due to secondary failure of diet therapy at 5–7 years.
HOMA=Homeostasis Model Assessment; data expressed as percentages of values in lean nondiabetic HOMA=Homeostasis Model Assessment; data expressed as percentages of values in lean nondiabetic reference population.reference population.Adapted from Levy J et al. Adapted from Levy J et al. Diabet Med.Diabet Med. 1998;15:290–296. 1998;15:290–296.
00
4040
6060
HO
MA
(%
)H
OM
A (
%)
2020
0000
4040
6060
8080
HO
MA
(H
OM
A (
%)
%)
2020
22 44 66 00 22 44 66
Years from diagnosisYears from diagnosis
-Cell Function-Cell Function Insulin SensitivityInsulin Sensitivity
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Hypothetical Model for Postnatal Pancreaticß-Cell Growth in Humans
CJ Rhodes, Science, 2005
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• At start of UKPDS,-cell function was already compromised
-cell function deteriorates over time (~4%/year)
Adapted from: UKPDS 16. Diabetes 1995;44:1249–1258.HOMA: homeostasis model assessment. n=4209
Extrapolation of -cell function prior to UKPDS
-ce
ll fu
nct
ion (
%,
HO
MA
)
Years from diagnosis
UKPDS
0
20
40
100
–4 6–10 –8 –6 –2 0 2 4
80
60
Diet
SulphonylureaMetformin
UKPDS: Loss of -cell function is the major determinant of disease progression in T2DM
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Il volume -cellulare èridotto del 40% già inpresenza di IFG
Lo studio dei pancreasautoptici ha dimostrato cheil volume relativo -cellularedei soggetti obesi con IFGe dei soggetti con diabetedi tipo 2 è rispettivamenteridotto del 40 e del 63% rispetto a quello dei soggettiobesi non-diabetici
Butler AE, et al. Diabetes 52:102-110, 2003
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Determinants of progressive loss of -cell function and mass
• Glucotoxicity
• Lipotoxicity
• Secretory defects
• Inflammation
• Islet amyloid deposition
• Incretin failure
• alpha-cell dysfunction
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Determinants of progressive loss of -cell function and mass
• Glucotoxicity reversible, tend to resolve after
• Lipotoxicity normalization of glucose by any mean
• Secretory defects
• Inflammation
• Islet amyloid deposition
• Incretin failure
• alpha-cell dysfunction
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Determinants of progressive loss of -cell function and mass
• Glucotoxicity
• Lipotoxicity
• Secretory defects: early, selective for glucose
• Inflammation
• Islet amyloid deposition
• Incretin failure
• alpha-cell dysfunction
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Perdita della Fase Precoce della Secrezione Insulinica nel Diabete Tipo 2
Ward WK, et al. Diabetes Care 1984;7:491–502.
Controllo Diabete di Tipo 2
120
100
80
60
40
20
0–30 0 30 60 90 120
Tempo (minuti)
–30 0 30 60 90 120
Tempo (minuti)
IRI
pla
smat
ica
(µ
U/m
l) 120
100
80
60
40
20
0IR
I p
lasm
atic
a (µ
U/m
l)
20 g glucosio20 g
glucosio
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• Glucotoxicity
• Lipotoxicity
• Secretory defects
• Inflammation: mediated by IL-1, IL-6, TNF-
• Islet amyloid deposition
• Incretin failure
• alpha-cell dysfunction
Determinants of progressive loss of -cell function and mass
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Interleukin-1–Receptor Antagonist in Type 2 Diabetes Mellitus Larsen CM et Al NEJM 356:1517 - 1526, 2007
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Determinants of progressive loss of -cell function and mass
• Glucotoxicity
• Lipotoxicity
• Secretory defects
• Inflammation
• Islet amyloid deposition: IAPP (Amylin)
• Incretin failure
• alpha-cell dysfunction
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Rhodes C. Science 307:380-384, 2005
Morfologia del pancreasendocrino nel normale, nell’obeso non diabetico enel diabetico di tipo 2
Nell’obeso non-diabetico ilnumero delle isole è aumentatoe le isole tendono ad esserepiù grandi, principalmente perun aumento delle -cellule
Nel diabetico di tipo 2, il numerodelle isole è diminuito, c’è unariduzione marcata delle -cellulee compaiono depositi di amiloide (in viola) che occupano buona parte dell’isola
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Diffuse islet amyloidosis
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Diffuse islet amyloidosis
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Human islet amyloid polypeptide (IAPP). The amyloidogenic region of IAPP is responsible for providing a toxic conformational structure within the islets.
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Determinants of progressive loss of -cell function and mass
• Glucotoxicity
• Lipotoxicity
• Secretory defects
• Inflammation
• Islet amyloid deposition
• Incretin failure Incretins: GIP, GLP-1
• alpha-cell dysfunction
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The Glucoregulatory Role of GLP-1
Beta cells:Enhances glucose-dependent
insulin secretion
Adapted from Flint A, et al. J Clin Invest. 1998;101:515-520.; Adapted from Larsson H, et al. Acta Physiol Scand. 1997;160:413-422.; Adapted from Nauck MA, et al. Diabetologia. 1996;39:1546-1553.; Adapted from Drucker DJ. Diabetes. 1998;47:159-169.
Liver: ↓ Glucagon reduces
hepatic glucose output
Alpha cells:↓ Postprandial
glucagon secretion
Stomach: Helps regulate
gastric emptying
GLP-1 secreted upon the ingestion of food
Promotes satiety and reduces appetite
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GLP-1 stimulates -cell regeneration and mass in animal models
Farilla et al. Endocrinology 2003;144:5149–5158. Bulotta et al. J Mol Endocrinol 2002;29:347–360.
-cell neogenesis
-cell proliferation
-cell hypertrophy
-cell apoptosis
-cell regeneration and increased mass
-cell
Red arrows indicate effect of GLP-1
Key
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Reduced GLP-1 secretion in type 2 diabetes
T2D patients
* * **
*
**
0
5
10
15
20
0 60 120 180 240
Time (min)
GLP-1 (pM)
IGT
Normal
Source: Adapted from Toft-Nielsen et al. ( 2001): J Clin Endocrinol Metab 86:3717-3723
Mixed Meal
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The burden of Type 2 Diabetes
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Diabeticretinopathy
Leading causeof blindnessin working-ageadults1
Diabeticnephropathy
Leading cause of end-stage renal disease2
Cardiovasculardisease
Stroke
1.2- to 1.8-fold increase in stroke3
Diabeticneuropathy
Leading cause of non-traumatic lower extremity amputations5
75% diabetic patients die from CV events4
Type 2 diabetes is NOT a mild disease
1Fong DS, et al. Diabetes Care 2003;26 (Suppl. 1):S99–S102. 2Molitch ME, et al. Diabetes Care 2003;26 (Suppl. 1):S94–S98. 3Kannel WB, et al. Am Heart J 1990;120:672–676. 4Gray RP & Yudkin JS. In Textbook of Diabetes 1997.
5Mayfield JA, et al. Diabetes Care 2003;26 (Suppl. 1):S78–S79.
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Complication
Retinopathy 21
Abnormal ECG 18
Absent foot pulses ( 2) and/or ischaemic feet 14
Impaired reflexes and/or decreased vibration sense 7
Angina 3
Intermittent claudication 3
Myocardial infarction 2
Stroke/transient ischaemic attack 1
Prevalence (%)*
*Some patients had more than one complication at time of diagnosis
Adapted from UKPDS VIII. Diabetologia 1991;34:877–890.
Serious complications of type 2 diabetes are present at diagnosis
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4 5
Type 2 diabetes increases the risk of CVD
*P < 0.1; †P < 0.05; ‡P < 0.01; §P < 0.001
1 2 3 6
Coronary mortality
Sudden death
Angina pectoris
MI
CHD
Cardiac failure
Intermittent claudication
Stroke
Any CV event§
*
§
†
§
†§
†‡
§
†
†
Males with diabetes
Females with diabetes
‡
Age-adjusted risk ratio(1 = risk for individuals without diabetes)
Adapted from Kannel WB, et al. Am Heart J 1990;120:672–676.
N/A
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Relative cost of diabetes
US data from 1990–1993 Adapted from www.cdc.gov/diabetes/pubs/costs/index.htm. Accessed 1 August, 2006.
120
Dir
ect
and
in
dir
ect
cost
s(U
S$
bil
lio
n)
0
20
40
60
80
100
Stroke Depression Arthritis Diabetes Cancer
$92
$104
$65
$44
$30
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Aggressive Glycemic Control in T2DM Reduces Risk of Complications
Risk Reduction With 1% Decline in Updated HbA1c
Micro-vasculardisease
PVD* MI Stroke Heartfailure
Cataractextraction
Death related to diabetes
P <.0001P <.0001 P =.035 P =.021 P <.0001
37% 43%
14% 12% 16% 19% 21%
15
PVD = Peripheral Vascular Disease; MI = Myocardial Infarction*UKPDS 35: Prospective observational analysis of UKPDS patients (n = 4585, incidence analysis; n = 3642, relative risk analysis). Median 10.0 years of follow up.Adapted from Stratton IM, et al. BMJ. 2000;321:405-412.
0
45
30
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Therapeutic Goals in Type 2 Diabetes
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ADA = American Diabetes Association; ACE = American College of Endocrinology; IDF = International Diabetes Federation*Referenced to a non-diabetic range of 4.0%–6.0% using a DCCT-based assay; †Upper limit of normal = 6.0%‡Measurements should be made 1–2 hours after the beginning of the mealAdapted from American Diabetes Association. Diabetes Care. 2005;28(supp 1):S4-S36. International Diabetes Federation. Global Guideline for Type 2 Diabetes. Brussels: International Diabetes Federation, 2005. American Association of Clinical Endocrinologists and the American College of Endocrinology. Endocrine Practice. 2002;8(suppl 1): 5-11.
ADA ACE IDF
HbA1c
< 6.0%* (individual goal)
< 7.0%* (general goal)
≤ 6.5%† < 6.5%*
Preprandial capillary plasma glucose
90–130 mg/dL
(5.0–7.2 mmol/L)
< 110 mg/dL
(< 6.0 mmol/L)
< 110 mg/dL
(< 6.0 mmol/L)
Peak postprandial capillary plasma glucose‡
< 180 mg/dL
(< 10.0 mmol/L)
< 140 mg/dL
(< 7.7 mmol/L)
< 145 mg/dL
(< 8.0 mmol/L)
Current Treatment Goals for Glycemic Control: Towards Reducing Risk of Complications
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1NHANES 1999–2000 DataT2DM represents ~90%–95% of casesAdapted from Adapted from Saydah SH, et al. JAMA. 2004;291:335-342.
Two Thirds of People with Type 2 Diabetes are Not at Goal1
HbA1c Level % Patients
<7.0% 37.0
7.0%–8.0% 25.8
>8.0% 37.2
>9.0% 20.2
>10.0% 12.4
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UKPDS: type 2 diabetes is progressively worsening independently on current therapies
Adapted from: UKPDS 34. Lancet 1998:352:854–865. *Using diet initially then sulphonylureas, insulin and/or metformin if FPG > 15 mmol/l; †ADA clinical practice recommendations. n=5102
6
7
8
9
Media
n H
bA
1c
(%
)
Years from randomisation
Conventional*GlibenclamideChlorpropamideMetforminInsulin
6.2% – upper limit of normal range
Recommended treatment target ≤ 7.0†
2 4 6 8 100
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Determinants of type 2 diabetes and anti-diabetic agents
Insulin resistance Metformin, TZDs, insulinLoss of -cell function• Glucotoxicity Any anti-diabetic• Lipotoxicity Any anti-diabetic• Secretory defects Sulfonylureas, Glinides, insulin• Inflammation TZDs (mild), anti-IL1 (exp)• Islet amyloid deposition None (?TZDs)• Incretin failure Incretin mimetics, analogues,
DPP-4 inhibitors• alpha-cell dysfunction Idem, insulin
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Metformin
TZDs
α-Glucosidase inhibitors
GI effects (nausea, diarrhea), lactic acidosis (rare)
GI effects (flatulence, diarrhea)
Weight gain, edema, fractures, ?CHF
Incretin mimetics (injection)
GI effects (nausea, vomiting, diarrhea)
SUs
Glinides
Hypoglycemia, weight gain, hyperinsulinemia*
Major Adverse Events of Current Treatments for T2DM Limit Efficacy
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Lifesty
le Changes
Diet and Exercise
Oral Monotherapy
Standard Approach to the Management of T2DM: Treatment Intensification
Oral Combination ++
Oral + Insulin ++ ++
Insulin
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Adapted from Mudaliar S et al. In: Ellenberg and Rifkin’s Diabetes Mellitus, 6th ed. New York, NY: Appleton and Lange; 2003:531-557.
Add insulin
Oral agent 2 Oral agents
Inadequate nonpharmacologic
therapy
3 Oral agents
Historical Algorithm ofTherapy for Type 2 Diabetes
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Possible Alternative Algorithm ofTherapy for Type 2 Diabetes
Oral agent
2 Oral agents
3 Oral agents
Add Insulin Earlier in the Algorithm
• Severe symptoms
• Severe hyperglycaemia
• Ketosis
• Pregnancy
Inadequate nonpharmacologic
therapy
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The Number of Medications Taken Usually Increases With Duration of Disease
100
0
Be
ta-c
ell
fun
cti
on
(%
)
0 10 15–25
Diabetesdiagnosed
Insulin-based
regimens
Multidrugcombo
±insulin
Approximate time (years)
Monotherapyfailure
Requiring insulin
Dual-drugregimens
Monotherapy
80
60
40
20
IGT
IGT=impaired glucose tolerance.UKPDS 16. Diabetes. 1995;44:1249–1258. Turner RC et al. JAMA. 1999;281:2005–2012; Warren RE. Diabetes Res Clin Pract. 2004;65:S3–S8; Lebovitz HE. Med Clin N Am. 2004;88:847–863.
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Nathan DM et al, Diabetes Care, 2006; Diabetologia 2006
DiagnosisDiagnosis
Lifestyle Intervention + MetforminLifestyle Intervention + Metformin
NoNo Yes*Yes*A1C≥7%A1C≥7%
Add Basal Insulin#
(most effective)Add Basal Insulin#
(most effective)Add Sulfonylurea(least expensive)Add Sulfonylurea(least expensive)
Add Glitazone(no hypoglycemia)
Add Glitazone(no hypoglycemia)
NoNo Yes*Yes*A1C≥7%A1C≥7% NoNo Yes*Yes*A1C≥7%A1C≥7% NoNo Yes*Yes*A1C≥7%A1C≥7%
Intensify Insulin#Intensify Insulin# Add GlitazoneAdd Glitazone Add Basal Insulin#Add Basal Insulin# Add SulfonylureaAdd Sulfonylurea
Add Basal or Intensify Insulin#Add Basal or Intensify Insulin#
Intensive Insulin + Metformin ± GlitazoneIntensive Insulin + Metformin ± Glitazone
NoNo Yes*Yes* NoNo Yes*Yes*A1C≥7%A1C≥7%A1C≥7%A1C≥7%
Step 1
Step 2
Step 3
Management of Hyperglycemia in Type 2 Diabetes: ADA/EASD Consensus Algorithm for the Initiation and
Adjustment of Therapy
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Iperglicemia post-prandiale:HbA1c ~+1%
C=colazione; P=pranzo; C=cena.Adapted from Riddle M. Diabetes Care 1990;13:67686.
Glicem
ia p
lasm
ati
ca
(mg
/dl)
300
200
100
0
Momenti della giornata (ore)
06.00 12.00 18.00 24.00 06.00
Diabete non controllato (HbA1c ~8%)
Iperglicemia aDigiuno:
HbA1c ~+2%
C
P
C
HbA1c normale~5%
Nel DMT2 sono elevati sia i livelli di glicemia a digiuno sia i post-prandiali