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INCRETINS BASED THERAPY
HOW EARLY ?
MOHAMMAD O. DAOUD, MD
CONSULTANT ENDOCRINOLOGIST
KAMC –NGHA JEDDAH
AGENDA
Case oriented discussion
Combination Rx : Guidelines / Algorithms
Basal Insulin…what is next ?
DPP4 I / GLP1-RA Vs Bolus Insulin
Conclusion
CASE
A 51 year old male patient with type 2 DM diagnosed 6 years ago
Currently on Metformin 1 gm bd , Gliclazide MR 90 mg daily
Other Rx: ASA , Atorvastatin 40 mg , Lisinopril 10 mg
Excellent compliance to diet plan , activity and medication intake
Glucose monitoring is above target
What kind of monitoring would you like to know ?
Fasting , Pre-meals and @ Bed time
Vs
Fasting , Post-meals and @ Bed time
Post-prandial
hyperglycaemia
Post-prandial
hyperglycaemia
contributes HbA1c ~1%
B=breakfast; L=lunch; D=dinner.
Adapted from Riddle MC. Diabetes Care. 1990;13:676-686.
Plasmaglucose(mg/dL)
300
200
100
0
Time of day (h)
6 12 18 24 6
Uncontrolled Diabetes HbA1c 8.5%

B

L

D
Normal
HbA1c ~5%
Basal Hyperglycaemia Contributes More to Increased
HbA1c Levels Than Does Post-prandial Hyperglycaemia
Basal hyperglycaemia
contributes ~2%
Fasting
hyperglycaemia
Case # 1
With higher HbA1C :
Pre-meal glucose readings contribute more to
the HbA1C
With HbA1C closer to target ( ex: <8-8.5%)
Post-meal glucose readings contributes more to
the HbA1C value
ADA-2016
Breakfast Lunch Dinner Bedtime
Before After Before After Before After
Day1 12.7 11.0 9.2 9.8
Day2 10.4 10 12.5 11.9
Day3 13.5 13.5 9.6 9.8
Day4 14.7 12.9 10.5
Day5 11.8 13 11.5 10.5
SMBG Record … your assessment ?
CASE
A 55 year old male patient with type 2 DM
On Metformin 1 gm bd , Gliclazide MR 90 mg daily
BP 128/78 , BMI 32 kg/m2
Labs:
HbA1c 9.7 %
Serum Cr 65 ( e-GFR 86 ml/minute )
Urinalysis : Hematuria ( > 2 urine samples: to Urology for evaluation )
CASE
A 55 year old male patient with type 2 DM
On Metformin 1 gm bd , Gliclazide MR 90 mg daily
BP 128/78 , BMI 32 kg/m2
Labs:
HbA1c 9.7 %
Serum Cr 65 ( e-GFR 86 ml/minute )
Urinalysis : Hematuria ( > 2 urine samples: to Urology for evaluation )
-What is next ?
-Patient wants to avoid injections !!
CASE
A 55 year old male patient with type 2 DM
On Metformin 1 gm bd , Gliclazide MR 90 mg daily
Labs :
HbA1c 9.7 % Serum Cr 65 ( e-GFR 86 ml/minute )
DPP4 inhibitor was added at full dose ( Sitagliptin 100 or Linagliptin 5mg …)
Wants to avoid injectable Rx.
Pioglitazone use and risk of bladder cancer:
population based cohort study
What this study adds
The use of Pioglitazone was associated with an overall
63% increased risk of bladder cancer, with the risk
increasing with increasing duration of use and dose
HR 1.63 (95% CI 1.22 to 2.19)
The use of Rosiglitazone was not
Likely to be a drug specific and not a class effect
Marco Tuccori,et al ; BMJ 2016; 352 doi:
http://dx.doi.org/10.1136/bmj.i1541
(Published 30 March 2016)Cite this as: BMJ 2016;352:i1541
Breakfast Lunch Dinner Bedtime
Before After Before After Before After
Day1 11 11.0 9.2 9.8
Day2 10.4 10 10.3
Day3 9.5 11.2 10.6 10.5
Day4 11.9 10.8
Day5 11.0 13 11.5 9.5
SMBG on: MFN + SU + DPP4i 3 months later
CASE
A 51 year old male patient with type 2 DM ;
BMI 31kg/m2
On Metformin 1 gm bd , Gliclazide MR 90 mg daily & + DPP4 inhibitor
Labs 3 months late: HbA1c ( 9.7% to 9.1% )
Serum Cr 60 ( e-GFR 90 ml/minute )
So…3 oral agents at max doses … and still out of control ?
Type 2 DM
Medications Barriers
Efficacy Limits
Adverse Reaction
Hypoglycemia
Weight gain
GI side effects
PO / Injection / Frequency
Cost
Case
A 55 year old male patient with type 2 DM ;
BMI 32kg/m2
On Metformin 1 gm bd , Gliclazide MR 90 mg daily & + DPP4 inhibitor
Labs 3 months late: HbA1c ( 9.7% >>> 9.1% )
Serum Cr 60 ( e-GFR 90 ml/minute )
Does this patient need insulin?
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Metformin + basal insulin + mealtime insulin or GLP-1RA
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
TZD
DPP-4i
GLP-1RA
Insulin
SU
SU
TZD
Insulin
DPP-4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Metformin + basal insulin + mealtime insulin or GLP-1RA
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
DPP-4i
SU
SU
TZD
Insulin
DPP-
4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
HbA1c
9.7%
to
9.1%
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Basal insulin
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
DPP-4i
SU
SU
TZD
Insulin
DPP-
4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-
1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
Case # 1
Basal insulin
Effective
Easy choice : single injection /Pen
(at bedtime)
“Breaks the Ice”
Basal Insulin: Pharmacokinetics
InsulinType Onset Peak Duration
Glargine 1-2 hrs ------- 24 hrs
Glargine -300 1-2 hrs ------- 24 hrs
Detemir 2-4 hrs ------- Up to 24 hrs
Degludec 30-90 mins ------- > 42 hrs
NPH 2 hrs 4-6 hrs 8-12 hrs
Case # Basal Insulin
 Example: body weight 0f 80 kg
16-24 units (0.2-0.3 u/kg) of
Glargine or Detemir added at Bedtime
Degludec ;flexible time
Or
Start a dose of 10 units
 Titrate every 2-3 days
SA- GLA-11-11-04
32
In T2DM ‘Fix fasting first’ –will lower the entire plasma
glucose through 24 hr
Adapted from Polonsky K. N Engl J Med 1988;318:1231–9 and Hirsch I, et al. Clin Diabetes 2005;23:78–86.
Theoretical simulation of diurnal blood glucose profile
Time of day (hours)
400
300
200
100
0
06:00 06:0010:00 14:00 18:00 22:00 02:00
Plasmaglucose(mg/dL)
Normal
Meal Meal Meal
20
15
10
5
0
Plasmaglucose(mmol/L)
Hyperglycaemia due to an increase in fasting glucose
T2DM
Breakfast Lunch Dinner Bedtime
Before After Before After Before After
Day1 10 11.0 10.2 10
Day2 7.4 9.0 9.3
Day3 6.5 9.2 11.0 11
Day4 9.9 11.8
Day5 7.2 11 11.0 10.5
After add on Glargine /Detemir 24 units HS>> 40 u
SA- GLA-11-11-04
When Basal Insulin is “Not Enough”
• Step 1: Think first of titrating the basal insulin dose till reaching
FBG target (Often under-dosage) ; Max 0.5 units /kg
• Step 2: Shift to Basal Plus or Basal-bolus (MDI) regimen :
• Number of daily injections up to 4 (1+3)
• Inconvenience
• Risk of hypoglycemia & Weight gain
Or
Incretin-Based Rx
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Basal insulin
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
DPP-4i
SU
SU
TZD
Insulin
DPP-
4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-
1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
HbA1c
9.1
to
8.0%
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Basal insulin + Meal Related Insulin
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
DPP-4i
SU
SU
TZD
Insulin
DPP-
4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-
1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
ADA/EASD position statement 2015
DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose
co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione
Inzucchi et al. Diabetes Care 2015;38:140−149
Basal Insulin + GLP 1 RA
Healthy eating, weight control, increased physical activity
Not at target
HbA1c after
~3 months
Dual
therapy
Triple
therapy
Metformin
Combination
injectable
therapy
Monothera
py
Not at target
after 3 months:
combination
therapy
with insulin
SU
DPP-4i
GLP-
1RA
Insulin
SU
SU
TZD
Insulin
DPP-
4i
GLP-1
RA
SU
TZD
Insulin
Insulin
TZD
DPP-4i
GLP-
1RA
Not at target
HbA1c after
~3 months
TZD
SU
DPP-4i
GLP-
1RA
Insulin
Diseaseprogression
SU
TZD
DPP-4i
Insulin
SGLT-2i
Mechanism of action of GLP-1RAs and DPP-4
inhibitors
Food
Gut
Food-activated
GLP-1 response
The enzyme DPP-4
breaks down GLP-1
GLP-1RAs work like
natural GLP-1 and are
DPP-4-resistant
DPP-4
GLP-1R
Glucose-dependent insulin
secretion
Beta cell
DPP-4 inhibitors act to
block the DPP-4 enzyme
Additional physiological benefits are observed at pharmacological
levels of GLP-1
DPP-4is, dipeptidyl peptidase-4 inhibitors; GLP-1, glucagon-like peptide 1; GLP-1RAs, glucagon-like peptide 1 receptor agonists
Adapted from Holst et al.1
1. Holst JJ et al. Trends Mol Med 2008;14:161–168; 2. Flint A et al. Adv Ther 2011;28:213–226
 Gastric
emptying
Physiological
GLP-1 levels
Pharmacological
GLP-1 levels
GLP-1 effects
IncreasingplasmaGLP-1
concentrations
GLP-1RAs
DPP-4is
Insulin
 Glucagon
=  Plasma glucose2
 Appetite
 Food intake
= Weight loss2
The Incretin Therapy
Short Acting
– Exenatide bid
Lixisenatide OD
Long Acting:
Liraglutide
Exenatide LAR
Dulaglutide
Albiglutide
(Semaglutide)
 Incretin mimetics: GLP-1 receptor agonists
Stable peptide analogues of GLP-1
– Post-Prandial Glucose – Fasting Glucose
GLP-1RA vs. DPP-4 inhibitor: change in HbA1c
Data are LS mean. *p<0.0001 vs. sitagliptin; †p=0.01 vs. liraglutide 1.2 mg
Pratley et al. Int J Clin Pract 2011;65:397–407; Bergenstal et al. Lancet 2010;376:431–9
Baseline HbA1c:
LIRA–DPP-4i (52 weeks)
ChangeinHbA1c(%)
p<0.0001
p<0.0001
ADA target
(<7.0%)
27% 50%* 63%*†
DURATION-2 (26 weeks)
ChangeinHbA1c(%)
p<0.0001
Sitagliptin
100 mg OD
Exenatide
2 mg OW
Sitagliptin
100 mg OD
Liraglutide
1.2 mg OD
Liraglutide
1.8 mg OD
Baseline HbA1c: 8.5% 8.6% 8.5% 8.4% 8.4%
~30% ~58%*
GLP-1RA vs. DPP-4 inhibitor: change in body weight
Changeinbodyweight(kg)
p<0.0001
p<0.0001
Data are LS mean
Pratley et al. Int J Clin Pract 2011;65:397–407; Bergenstal et al. Lancet 2010;376:431–9
Changeinbodyweight(kg)
p=0.0002
Baseline
body weight: 87 kg 89 kg 93 kg 94 kg 95 kg
LIRA–DPP-4i (52 weeks)DURATION-2 (26 weeks)
Sitagliptin
100 mg OD
Exenatide
2 mg OW
Sitagliptin
100 mg OD
Liraglutide
1.2 mg OD
Liraglutide
1.8 mg OD
DURATION-2: safety and tolerability from Week 0 to
Week 26
Bergenstal et al. Lancet 2010;376;431–9; Bydureon. EMA: Summary of Product Characteristics. 2011;
available from: http://www.medicines.org.uk/emc/medicine/24665/SPC/ (accessed 2 November 2011)
0
5
10
15
20
25
30
35
40
Exenatide OW (100 mg) Sitagliptin (100 mg)
Adverseevents(%)
Nausea Diarrhoea Vomiting Injection site pruritis
• Incidence of minor hypoglycaemia was low and similar between
groups (1–3%)
• Nausea was predominantly mild
Switching from DPP-4 inhibitor to a GLP-1RA: change in
HbA1c
Data are LS mean. †Mean HbA1c at week 26 for all core study participants; *p<0.05 for change from switch
Pratley et al. Diabetes Care 2012;DOI:10.2337/dc11-2113; Wysham et al. Diabetic Medicine 2011;28:705–14
LIRA–DPP-4i
(Weeks 52–78)
ChangeinHbA1c(%)
p=0.006
p=0.0001
ADA target HbA1c
<7.0%
DURATION-2
(Weeks 26–52)
ChangeinHbA1c(%)
p=0.001
Week 26 HbA1c:
7.2% 7.6%
Week 52 HbA1c:
7.6%†
Sitalira 1.2 mg
Sitalira 1.8 mgSitaexenatide OW
50%*
30%30%
49%*
36%
53%*
Switching from a DPP-4 inhibitor to a GLP-1RA: change in body
weight
LIRA–DPP-4i
(Weeks 52–78)
Changeinbodyweight(kg)
p<0.0001
p<0.0001
Changeinbodyweight(kg)
p=0.0006
Week 26
body weight: 92.8 kg 91.6 kg
Week 52
body weight:
86 kg†
Sitalira 1.2 mg
Sitalira 1.8 mgSitaexenatide OW
Data are LS mean. †Mean body weight at week 26 for all core study participants
Pratley et al. Diabetes Care 2012;DOI:10.2337/dc11-2113; Wysham et al. Diabetic Medicine 2011;28:705–14
DURATION-2
(Weeks 26–52)
EASD-ADA
2015
Basal Insulin- GLP-1RA
The Evidence
GLP-1RA, glucagon-like peptide-1 receptor agonist
52
4B Study:
Basal insulin glargine + exenatide B.i.d.
treatment or Basal insulin glargine + mealtime
Bolus insulin lispro treatment.
Michaela Diamant, Diabetes Care 2014;37:2763–2773
53
Study Design
Entry Criteria:
• T2DM HbA1c >7.0 to ≤10%
• IG + MET with or w/o SU*
• IG ≥20 IU/day
*SU, sulfonylurea discontinued upon study entry; MET, metformin
1. Yki-Jarvinen H, et al. Diabetes Care. 2007;30:1364-1369; 2. Rosenstock J, al. Diabetes Care. 2008;31:20-25.
Week
Basal Insulin Optimization (BIO)
Titrated Basal IG1
12-wk BIO Phase
0 30
30-wk Intervention Phase
Ex-BID 5mg Ex-BID 10mg
LisTID2
Titrated Basal IG1
+ MET continued throughout study
Randomization
-12-14
Screening
Michaela Diamant, Diabetes Care 2014;37:2763–2773
54
Titration of Basal Insulin Glargine Once Daily
( IG QD), Byetta and Prandial Lispro TID
Target fasting glucose <5.6 mmol/L (<100 mg/dL) with no hypoglycemia
BIO-phase: IG QD1
Lis TID2
Target pre-prandial glucose <6.1 mmol/L
(<109mg/dL) with no hypoglycemia
ExBID
Dose increased at wk 4 and tapered
thereafter if side-effects occurred
Target fasting glucose <5.6 mmol/L (<100 mg/dL) with no hypoglycemia
Intervention phase: IG QD1
ExBID+IG arm
IG decreased by ≥10% if HbA1c ≤8.0% &
at wk 4 with ExBID dose↑
LisTID+IG arm
½ up to ⅔ of IG daily dose maintained,
⅓- ½ divided into 3 pre-meal doses of Lis
At Randomization
Michaela Diamant, Diabetes Care 2014;37:2763–2773
55
Results: HbA1c at 30 Weeks
Values are LS Mean ± SE calculated using MMRM; *N’s for target achievement are patients with HbA1c values at 30 wk
Michaela Diamant, Diabetes Care 2014;37:2763–2773
56
Results: Fasting and Self-Measured Glucose
Per protocol population (N=510), Fasting glucose values are LS Mean ± SE; blood glucose values are Mean ± SE; *P<0.0001
Michaela Diamant, Diabetes Care 2014;37:2763–2773
57
Results: Mean Daily Insulin Doses
Per protocol population (N=510), Values are Mean ± SD
Michaela Diamant, Diabetes Care 2014;37:2763–2773
58
Results: Change in Body Weight
Michaela Diamant, Diabetes Care 2014;37:2763–2773
59
Results: Incidence of Hypoglycemia
Overall Rate per patient-year (Minor and Major): 2.1 (ExBID + IG) vs. 5.1 (LisTID + IG)
Michaela Diamant, Diabetes Care 2014;37:2763–2773
Conclusions:
Adding Exenatide to titrated Glargine with Metformin
resulted in similar glycemic control as add on Lispro insulin
GLP1- RA (Exenatide) is a safe, effective and well tolerated
non insulin Rx if Basal insulin fails
TAKE HOME MESSAGES
Compared with DPP-4 inhibitors, GLP-1 RA are associated with:
1-Greater HbA1c reduction and greater weight loss
2-Similar low risk of hypo-glycaemia but
an increased incidence of gastrointestinal events
Switching from a DPP-4 i to a GLP-1 RA was associated with:
1-Significant additional HbA1c reductions
2-Significant weight loss
Incretins based therapy ( DPP4 I and GLP1-RA) provides an
excellent combination with Insulin :Basal and MDI
GLP1-RA is an excellent effective alternative to
meal related insulin on top of basal insulin with:
-Equal postprandial efficacy
-Same or better HbA1c lowering and
-Same /lower risk of hypoglycemia
- Weight loss
GLP-1
1 .
2 .
3 .
SGLT2DPP4Metformin

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Incretins based therapy :How Early

  • 1. INCRETINS BASED THERAPY HOW EARLY ? MOHAMMAD O. DAOUD, MD CONSULTANT ENDOCRINOLOGIST KAMC –NGHA JEDDAH
  • 2. AGENDA Case oriented discussion Combination Rx : Guidelines / Algorithms Basal Insulin…what is next ? DPP4 I / GLP1-RA Vs Bolus Insulin Conclusion
  • 3. CASE A 51 year old male patient with type 2 DM diagnosed 6 years ago Currently on Metformin 1 gm bd , Gliclazide MR 90 mg daily Other Rx: ASA , Atorvastatin 40 mg , Lisinopril 10 mg Excellent compliance to diet plan , activity and medication intake Glucose monitoring is above target
  • 4. What kind of monitoring would you like to know ? Fasting , Pre-meals and @ Bed time Vs Fasting , Post-meals and @ Bed time
  • 5. Post-prandial hyperglycaemia Post-prandial hyperglycaemia contributes HbA1c ~1% B=breakfast; L=lunch; D=dinner. Adapted from Riddle MC. Diabetes Care. 1990;13:676-686. Plasmaglucose(mg/dL) 300 200 100 0 Time of day (h) 6 12 18 24 6 Uncontrolled Diabetes HbA1c 8.5%  B  L  D Normal HbA1c ~5% Basal Hyperglycaemia Contributes More to Increased HbA1c Levels Than Does Post-prandial Hyperglycaemia Basal hyperglycaemia contributes ~2% Fasting hyperglycaemia
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  • 7. Case # 1 With higher HbA1C : Pre-meal glucose readings contribute more to the HbA1C With HbA1C closer to target ( ex: <8-8.5%) Post-meal glucose readings contributes more to the HbA1C value
  • 9. Breakfast Lunch Dinner Bedtime Before After Before After Before After Day1 12.7 11.0 9.2 9.8 Day2 10.4 10 12.5 11.9 Day3 13.5 13.5 9.6 9.8 Day4 14.7 12.9 10.5 Day5 11.8 13 11.5 10.5 SMBG Record … your assessment ?
  • 10. CASE A 55 year old male patient with type 2 DM On Metformin 1 gm bd , Gliclazide MR 90 mg daily BP 128/78 , BMI 32 kg/m2 Labs: HbA1c 9.7 % Serum Cr 65 ( e-GFR 86 ml/minute ) Urinalysis : Hematuria ( > 2 urine samples: to Urology for evaluation )
  • 11. CASE A 55 year old male patient with type 2 DM On Metformin 1 gm bd , Gliclazide MR 90 mg daily BP 128/78 , BMI 32 kg/m2 Labs: HbA1c 9.7 % Serum Cr 65 ( e-GFR 86 ml/minute ) Urinalysis : Hematuria ( > 2 urine samples: to Urology for evaluation ) -What is next ? -Patient wants to avoid injections !!
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  • 14. CASE A 55 year old male patient with type 2 DM On Metformin 1 gm bd , Gliclazide MR 90 mg daily Labs : HbA1c 9.7 % Serum Cr 65 ( e-GFR 86 ml/minute ) DPP4 inhibitor was added at full dose ( Sitagliptin 100 or Linagliptin 5mg …) Wants to avoid injectable Rx.
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  • 16. Pioglitazone use and risk of bladder cancer: population based cohort study What this study adds The use of Pioglitazone was associated with an overall 63% increased risk of bladder cancer, with the risk increasing with increasing duration of use and dose HR 1.63 (95% CI 1.22 to 2.19) The use of Rosiglitazone was not Likely to be a drug specific and not a class effect Marco Tuccori,et al ; BMJ 2016; 352 doi: http://dx.doi.org/10.1136/bmj.i1541 (Published 30 March 2016)Cite this as: BMJ 2016;352:i1541
  • 17. Breakfast Lunch Dinner Bedtime Before After Before After Before After Day1 11 11.0 9.2 9.8 Day2 10.4 10 10.3 Day3 9.5 11.2 10.6 10.5 Day4 11.9 10.8 Day5 11.0 13 11.5 9.5 SMBG on: MFN + SU + DPP4i 3 months later
  • 18. CASE A 51 year old male patient with type 2 DM ; BMI 31kg/m2 On Metformin 1 gm bd , Gliclazide MR 90 mg daily & + DPP4 inhibitor Labs 3 months late: HbA1c ( 9.7% to 9.1% ) Serum Cr 60 ( e-GFR 90 ml/minute ) So…3 oral agents at max doses … and still out of control ?
  • 19. Type 2 DM Medications Barriers Efficacy Limits Adverse Reaction Hypoglycemia Weight gain GI side effects PO / Injection / Frequency Cost
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  • 23. Case A 55 year old male patient with type 2 DM ; BMI 32kg/m2 On Metformin 1 gm bd , Gliclazide MR 90 mg daily & + DPP4 inhibitor Labs 3 months late: HbA1c ( 9.7% >>> 9.1% ) Serum Cr 60 ( e-GFR 90 ml/minute ) Does this patient need insulin?
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  • 26. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Metformin + basal insulin + mealtime insulin or GLP-1RA Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin TZD DPP-4i GLP-1RA Insulin SU SU TZD Insulin DPP-4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP-1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i
  • 27. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Metformin + basal insulin + mealtime insulin or GLP-1RA Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin DPP-4i SU SU TZD Insulin DPP- 4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP-1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i HbA1c 9.7% to 9.1%
  • 28. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Basal insulin Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin DPP-4i SU SU TZD Insulin DPP- 4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP- 1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i
  • 29. Case # 1 Basal insulin Effective Easy choice : single injection /Pen (at bedtime) “Breaks the Ice”
  • 30. Basal Insulin: Pharmacokinetics InsulinType Onset Peak Duration Glargine 1-2 hrs ------- 24 hrs Glargine -300 1-2 hrs ------- 24 hrs Detemir 2-4 hrs ------- Up to 24 hrs Degludec 30-90 mins ------- > 42 hrs NPH 2 hrs 4-6 hrs 8-12 hrs
  • 31. Case # Basal Insulin  Example: body weight 0f 80 kg 16-24 units (0.2-0.3 u/kg) of Glargine or Detemir added at Bedtime Degludec ;flexible time Or Start a dose of 10 units  Titrate every 2-3 days
  • 32. SA- GLA-11-11-04 32 In T2DM ‘Fix fasting first’ –will lower the entire plasma glucose through 24 hr Adapted from Polonsky K. N Engl J Med 1988;318:1231–9 and Hirsch I, et al. Clin Diabetes 2005;23:78–86. Theoretical simulation of diurnal blood glucose profile Time of day (hours) 400 300 200 100 0 06:00 06:0010:00 14:00 18:00 22:00 02:00 Plasmaglucose(mg/dL) Normal Meal Meal Meal 20 15 10 5 0 Plasmaglucose(mmol/L) Hyperglycaemia due to an increase in fasting glucose T2DM
  • 33. Breakfast Lunch Dinner Bedtime Before After Before After Before After Day1 10 11.0 10.2 10 Day2 7.4 9.0 9.3 Day3 6.5 9.2 11.0 11 Day4 9.9 11.8 Day5 7.2 11 11.0 10.5 After add on Glargine /Detemir 24 units HS>> 40 u
  • 34. SA- GLA-11-11-04 When Basal Insulin is “Not Enough” • Step 1: Think first of titrating the basal insulin dose till reaching FBG target (Often under-dosage) ; Max 0.5 units /kg • Step 2: Shift to Basal Plus or Basal-bolus (MDI) regimen : • Number of daily injections up to 4 (1+3) • Inconvenience • Risk of hypoglycemia & Weight gain Or Incretin-Based Rx
  • 35. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Basal insulin Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin DPP-4i SU SU TZD Insulin DPP- 4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP- 1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i HbA1c 9.1 to 8.0%
  • 36. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Basal insulin + Meal Related Insulin Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin DPP-4i SU SU TZD Insulin DPP- 4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP- 1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i
  • 37. ADA/EASD position statement 2015 DPP-4i, dipeptidyl peptidase-4 inhibitor; GLP-1RA, glucagon-like peptide-1 receptor agonist; SGLT-2i, sodium-glucose co-transporter-2 inhibitor; SU, sulphonylurea; TZD, thiazolidinedione Inzucchi et al. Diabetes Care 2015;38:140−149 Basal Insulin + GLP 1 RA Healthy eating, weight control, increased physical activity Not at target HbA1c after ~3 months Dual therapy Triple therapy Metformin Combination injectable therapy Monothera py Not at target after 3 months: combination therapy with insulin SU DPP-4i GLP- 1RA Insulin SU SU TZD Insulin DPP- 4i GLP-1 RA SU TZD Insulin Insulin TZD DPP-4i GLP- 1RA Not at target HbA1c after ~3 months TZD SU DPP-4i GLP- 1RA Insulin Diseaseprogression SU TZD DPP-4i Insulin SGLT-2i
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  • 39. Mechanism of action of GLP-1RAs and DPP-4 inhibitors Food Gut Food-activated GLP-1 response The enzyme DPP-4 breaks down GLP-1 GLP-1RAs work like natural GLP-1 and are DPP-4-resistant DPP-4 GLP-1R Glucose-dependent insulin secretion Beta cell DPP-4 inhibitors act to block the DPP-4 enzyme
  • 40. Additional physiological benefits are observed at pharmacological levels of GLP-1 DPP-4is, dipeptidyl peptidase-4 inhibitors; GLP-1, glucagon-like peptide 1; GLP-1RAs, glucagon-like peptide 1 receptor agonists Adapted from Holst et al.1 1. Holst JJ et al. Trends Mol Med 2008;14:161–168; 2. Flint A et al. Adv Ther 2011;28:213–226  Gastric emptying Physiological GLP-1 levels Pharmacological GLP-1 levels GLP-1 effects IncreasingplasmaGLP-1 concentrations GLP-1RAs DPP-4is Insulin  Glucagon =  Plasma glucose2  Appetite  Food intake = Weight loss2
  • 41. The Incretin Therapy Short Acting – Exenatide bid Lixisenatide OD Long Acting: Liraglutide Exenatide LAR Dulaglutide Albiglutide (Semaglutide)  Incretin mimetics: GLP-1 receptor agonists Stable peptide analogues of GLP-1 – Post-Prandial Glucose – Fasting Glucose
  • 42. GLP-1RA vs. DPP-4 inhibitor: change in HbA1c Data are LS mean. *p<0.0001 vs. sitagliptin; †p=0.01 vs. liraglutide 1.2 mg Pratley et al. Int J Clin Pract 2011;65:397–407; Bergenstal et al. Lancet 2010;376:431–9 Baseline HbA1c: LIRA–DPP-4i (52 weeks) ChangeinHbA1c(%) p<0.0001 p<0.0001 ADA target (<7.0%) 27% 50%* 63%*† DURATION-2 (26 weeks) ChangeinHbA1c(%) p<0.0001 Sitagliptin 100 mg OD Exenatide 2 mg OW Sitagliptin 100 mg OD Liraglutide 1.2 mg OD Liraglutide 1.8 mg OD Baseline HbA1c: 8.5% 8.6% 8.5% 8.4% 8.4% ~30% ~58%*
  • 43. GLP-1RA vs. DPP-4 inhibitor: change in body weight Changeinbodyweight(kg) p<0.0001 p<0.0001 Data are LS mean Pratley et al. Int J Clin Pract 2011;65:397–407; Bergenstal et al. Lancet 2010;376:431–9 Changeinbodyweight(kg) p=0.0002 Baseline body weight: 87 kg 89 kg 93 kg 94 kg 95 kg LIRA–DPP-4i (52 weeks)DURATION-2 (26 weeks) Sitagliptin 100 mg OD Exenatide 2 mg OW Sitagliptin 100 mg OD Liraglutide 1.2 mg OD Liraglutide 1.8 mg OD
  • 44. DURATION-2: safety and tolerability from Week 0 to Week 26 Bergenstal et al. Lancet 2010;376;431–9; Bydureon. EMA: Summary of Product Characteristics. 2011; available from: http://www.medicines.org.uk/emc/medicine/24665/SPC/ (accessed 2 November 2011) 0 5 10 15 20 25 30 35 40 Exenatide OW (100 mg) Sitagliptin (100 mg) Adverseevents(%) Nausea Diarrhoea Vomiting Injection site pruritis • Incidence of minor hypoglycaemia was low and similar between groups (1–3%) • Nausea was predominantly mild
  • 45. Switching from DPP-4 inhibitor to a GLP-1RA: change in HbA1c Data are LS mean. †Mean HbA1c at week 26 for all core study participants; *p<0.05 for change from switch Pratley et al. Diabetes Care 2012;DOI:10.2337/dc11-2113; Wysham et al. Diabetic Medicine 2011;28:705–14 LIRA–DPP-4i (Weeks 52–78) ChangeinHbA1c(%) p=0.006 p=0.0001 ADA target HbA1c <7.0% DURATION-2 (Weeks 26–52) ChangeinHbA1c(%) p=0.001 Week 26 HbA1c: 7.2% 7.6% Week 52 HbA1c: 7.6%† Sitalira 1.2 mg Sitalira 1.8 mgSitaexenatide OW 50%* 30%30% 49%* 36% 53%*
  • 46. Switching from a DPP-4 inhibitor to a GLP-1RA: change in body weight LIRA–DPP-4i (Weeks 52–78) Changeinbodyweight(kg) p<0.0001 p<0.0001 Changeinbodyweight(kg) p=0.0006 Week 26 body weight: 92.8 kg 91.6 kg Week 52 body weight: 86 kg† Sitalira 1.2 mg Sitalira 1.8 mgSitaexenatide OW Data are LS mean. †Mean body weight at week 26 for all core study participants Pratley et al. Diabetes Care 2012;DOI:10.2337/dc11-2113; Wysham et al. Diabetic Medicine 2011;28:705–14 DURATION-2 (Weeks 26–52)
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  • 49. Basal Insulin- GLP-1RA The Evidence GLP-1RA, glucagon-like peptide-1 receptor agonist
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  • 52. 52 4B Study: Basal insulin glargine + exenatide B.i.d. treatment or Basal insulin glargine + mealtime Bolus insulin lispro treatment. Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 53. 53 Study Design Entry Criteria: • T2DM HbA1c >7.0 to ≤10% • IG + MET with or w/o SU* • IG ≥20 IU/day *SU, sulfonylurea discontinued upon study entry; MET, metformin 1. Yki-Jarvinen H, et al. Diabetes Care. 2007;30:1364-1369; 2. Rosenstock J, al. Diabetes Care. 2008;31:20-25. Week Basal Insulin Optimization (BIO) Titrated Basal IG1 12-wk BIO Phase 0 30 30-wk Intervention Phase Ex-BID 5mg Ex-BID 10mg LisTID2 Titrated Basal IG1 + MET continued throughout study Randomization -12-14 Screening Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 54. 54 Titration of Basal Insulin Glargine Once Daily ( IG QD), Byetta and Prandial Lispro TID Target fasting glucose <5.6 mmol/L (<100 mg/dL) with no hypoglycemia BIO-phase: IG QD1 Lis TID2 Target pre-prandial glucose <6.1 mmol/L (<109mg/dL) with no hypoglycemia ExBID Dose increased at wk 4 and tapered thereafter if side-effects occurred Target fasting glucose <5.6 mmol/L (<100 mg/dL) with no hypoglycemia Intervention phase: IG QD1 ExBID+IG arm IG decreased by ≥10% if HbA1c ≤8.0% & at wk 4 with ExBID dose↑ LisTID+IG arm ½ up to ⅔ of IG daily dose maintained, ⅓- ½ divided into 3 pre-meal doses of Lis At Randomization Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 55. 55 Results: HbA1c at 30 Weeks Values are LS Mean ± SE calculated using MMRM; *N’s for target achievement are patients with HbA1c values at 30 wk Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 56. 56 Results: Fasting and Self-Measured Glucose Per protocol population (N=510), Fasting glucose values are LS Mean ± SE; blood glucose values are Mean ± SE; *P<0.0001 Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 57. 57 Results: Mean Daily Insulin Doses Per protocol population (N=510), Values are Mean ± SD Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 58. 58 Results: Change in Body Weight Michaela Diamant, Diabetes Care 2014;37:2763–2773
  • 59. 59 Results: Incidence of Hypoglycemia Overall Rate per patient-year (Minor and Major): 2.1 (ExBID + IG) vs. 5.1 (LisTID + IG) Michaela Diamant, Diabetes Care 2014;37:2763–2773 Conclusions: Adding Exenatide to titrated Glargine with Metformin resulted in similar glycemic control as add on Lispro insulin GLP1- RA (Exenatide) is a safe, effective and well tolerated non insulin Rx if Basal insulin fails
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  • 63. Compared with DPP-4 inhibitors, GLP-1 RA are associated with: 1-Greater HbA1c reduction and greater weight loss 2-Similar low risk of hypo-glycaemia but an increased incidence of gastrointestinal events Switching from a DPP-4 i to a GLP-1 RA was associated with: 1-Significant additional HbA1c reductions 2-Significant weight loss
  • 64. Incretins based therapy ( DPP4 I and GLP1-RA) provides an excellent combination with Insulin :Basal and MDI GLP1-RA is an excellent effective alternative to meal related insulin on top of basal insulin with: -Equal postprandial efficacy -Same or better HbA1c lowering and -Same /lower risk of hypoglycemia - Weight loss
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  • 66. GLP-1 1 . 2 . 3 . SGLT2DPP4Metformin