Noninsulin agents that could be used for management of early post–renal transplant hyperglycemia
Noninsulin agent . | Considerations for use in EPTH . | Reference studies . | Comments . |
---|---|---|---|
Metformin | o Avoid with tenuous renal function | Not favored in EPTH | |
o Gastrointestinal upset | |||
o Can rarely cause lactic acidosis in impaired renal function | |||
Sulfonylurea | o Require dose adjustment with renal function, which varies in the early posttransplant period | Not favored in EPTH | |
o High risk of hypoglycemia | |||
o Weight gain | |||
GLP-1 RA | o Potential risk of acute kidney injury with higher dose | (83–85) | Need further studies for use in EPTH |
o Cardiovascular benefit | |||
o Weight loss | |||
DPP-4 inhibitors | o Better HOMA-IR and HOMA-B compared to insulin | (86–91) | Favorable studies, need randomized controlled trials to compare glycemic control for EPTH |
o Linagliptin does not require renal dose adjustment | |||
SGLT2 inhibitors | o Avoidance with tenuous kidney function | (92) | Need further studies for use in EPTH |
o Potential for causing dehydration | |||
o Genitourinary infections | |||
o Weight loss | |||
o Blood pressure control | |||
o Increased risk of volume depletion and ketoacidosis perioperatively | |||
o Canagliflozin showed glycemic improvement at 6 months post transplant without significant adverse effects | |||
Thiazolidinediones | o Potential for fluid retention | Not favored | |
o Slow onset of action in improving hyperglycemia | |||
o Weight gain | |||
o Increased risk for heart failure |
Noninsulin agent . | Considerations for use in EPTH . | Reference studies . | Comments . |
---|---|---|---|
Metformin | o Avoid with tenuous renal function | Not favored in EPTH | |
o Gastrointestinal upset | |||
o Can rarely cause lactic acidosis in impaired renal function | |||
Sulfonylurea | o Require dose adjustment with renal function, which varies in the early posttransplant period | Not favored in EPTH | |
o High risk of hypoglycemia | |||
o Weight gain | |||
GLP-1 RA | o Potential risk of acute kidney injury with higher dose | (83–85) | Need further studies for use in EPTH |
o Cardiovascular benefit | |||
o Weight loss | |||
DPP-4 inhibitors | o Better HOMA-IR and HOMA-B compared to insulin | (86–91) | Favorable studies, need randomized controlled trials to compare glycemic control for EPTH |
o Linagliptin does not require renal dose adjustment | |||
SGLT2 inhibitors | o Avoidance with tenuous kidney function | (92) | Need further studies for use in EPTH |
o Potential for causing dehydration | |||
o Genitourinary infections | |||
o Weight loss | |||
o Blood pressure control | |||
o Increased risk of volume depletion and ketoacidosis perioperatively | |||
o Canagliflozin showed glycemic improvement at 6 months post transplant without significant adverse effects | |||
Thiazolidinediones | o Potential for fluid retention | Not favored | |
o Slow onset of action in improving hyperglycemia | |||
o Weight gain | |||
o Increased risk for heart failure |
Abbreviations: DPP-4, dipeptidyl peptidase-4; EPTH, early post–renal transplant hyperglycemia; GLP-1 RA, glucagon-like peptide-1 receptor agonist; HOMA-B, homeostatic model assessment of β-cell function; HOMA-IR, homeostatic model assessment of insulin resistance; SGLT2, sodium-glucose cotransporter-2.
Noninsulin agents that could be used for management of early post–renal transplant hyperglycemia
Noninsulin agent . | Considerations for use in EPTH . | Reference studies . | Comments . |
---|---|---|---|
Metformin | o Avoid with tenuous renal function | Not favored in EPTH | |
o Gastrointestinal upset | |||
o Can rarely cause lactic acidosis in impaired renal function | |||
Sulfonylurea | o Require dose adjustment with renal function, which varies in the early posttransplant period | Not favored in EPTH | |
o High risk of hypoglycemia | |||
o Weight gain | |||
GLP-1 RA | o Potential risk of acute kidney injury with higher dose | (83–85) | Need further studies for use in EPTH |
o Cardiovascular benefit | |||
o Weight loss | |||
DPP-4 inhibitors | o Better HOMA-IR and HOMA-B compared to insulin | (86–91) | Favorable studies, need randomized controlled trials to compare glycemic control for EPTH |
o Linagliptin does not require renal dose adjustment | |||
SGLT2 inhibitors | o Avoidance with tenuous kidney function | (92) | Need further studies for use in EPTH |
o Potential for causing dehydration | |||
o Genitourinary infections | |||
o Weight loss | |||
o Blood pressure control | |||
o Increased risk of volume depletion and ketoacidosis perioperatively | |||
o Canagliflozin showed glycemic improvement at 6 months post transplant without significant adverse effects | |||
Thiazolidinediones | o Potential for fluid retention | Not favored | |
o Slow onset of action in improving hyperglycemia | |||
o Weight gain | |||
o Increased risk for heart failure |
Noninsulin agent . | Considerations for use in EPTH . | Reference studies . | Comments . |
---|---|---|---|
Metformin | o Avoid with tenuous renal function | Not favored in EPTH | |
o Gastrointestinal upset | |||
o Can rarely cause lactic acidosis in impaired renal function | |||
Sulfonylurea | o Require dose adjustment with renal function, which varies in the early posttransplant period | Not favored in EPTH | |
o High risk of hypoglycemia | |||
o Weight gain | |||
GLP-1 RA | o Potential risk of acute kidney injury with higher dose | (83–85) | Need further studies for use in EPTH |
o Cardiovascular benefit | |||
o Weight loss | |||
DPP-4 inhibitors | o Better HOMA-IR and HOMA-B compared to insulin | (86–91) | Favorable studies, need randomized controlled trials to compare glycemic control for EPTH |
o Linagliptin does not require renal dose adjustment | |||
SGLT2 inhibitors | o Avoidance with tenuous kidney function | (92) | Need further studies for use in EPTH |
o Potential for causing dehydration | |||
o Genitourinary infections | |||
o Weight loss | |||
o Blood pressure control | |||
o Increased risk of volume depletion and ketoacidosis perioperatively | |||
o Canagliflozin showed glycemic improvement at 6 months post transplant without significant adverse effects | |||
Thiazolidinediones | o Potential for fluid retention | Not favored | |
o Slow onset of action in improving hyperglycemia | |||
o Weight gain | |||
o Increased risk for heart failure |
Abbreviations: DPP-4, dipeptidyl peptidase-4; EPTH, early post–renal transplant hyperglycemia; GLP-1 RA, glucagon-like peptide-1 receptor agonist; HOMA-B, homeostatic model assessment of β-cell function; HOMA-IR, homeostatic model assessment of insulin resistance; SGLT2, sodium-glucose cotransporter-2.
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