Medications to Prevent Alcohol Cravings in Patients with Diabetes Mellitus
Naltrexone and acamprosate are FDA-approved medications for reducing alcohol cravings and maintaining abstinence in patients with alcohol use disorder, and both can be used in patients with diabetes mellitus, though careful glucose monitoring is essential due to alcohol's complex effects on glycemic control. 1, 2
FDA-Approved Anti-Craving Medications
Naltrexone
- Naltrexone 50 mg once daily is an opioid receptor antagonist that blocks endogenous opioid effects and reduces alcohol consumption without causing aversive reactions. 1
- The medication works by competitively binding to opioid receptors, blocking the rewarding effects of alcohol, and has been shown to reduce alcohol consumption in clinical studies as an adjunct to psychosocial support. 1
- Naltrexone is well-absorbed orally but undergoes significant first-pass metabolism with bioavailability of 5-40%, and does not accumulate with daily dosing. 1
- Critical consideration for diabetes patients: Naltrexone itself does not directly affect glucose metabolism, but by reducing alcohol intake, it helps prevent alcohol-related hypoglycemia and hyperglycemia. 1
Acamprosate
- Acamprosate calcium 666 mg (two 333 mg tablets) three times daily is indicated for maintaining abstinence from alcohol in patients who are already abstinent at treatment initiation. 2
- The medication should be started as soon as possible after alcohol withdrawal when abstinence is achieved, and must be part of a comprehensive psychosocial treatment program. 2
- Dose adjustment required in diabetes patients with renal complications: For moderate renal impairment (creatinine clearance 30-50 mL/min), reduce to 333 mg three times daily; contraindicated if creatinine clearance ≤30 mL/min. 2
- Acamprosate can be taken without regard to meals, though dosing with meals was used in clinical trials and may be preferable for patients eating three regular meals daily. 2
Critical Diabetes-Specific Considerations
Alcohol's Effects on Glucose Metabolism
- Alcohol inhibits both gluconeogenesis and glycogenolysis, creating significant hypoglycemia risk, especially in patients using insulin or insulin secretagogues (sulfonylureas, meglitinides). 3, 4
- When consumed with carbohydrate-containing meals, alcohol becomes the preferred fuel and may initially cause higher blood glucose levels followed by reactive hypoglycemia. 4
- Delayed hypoglycemia is a major concern, potentially occurring the morning after evening alcohol consumption, particularly in fasted states or with depleted glycogen stores. 3, 5
Monitoring Requirements During Treatment
- Patients must be educated to monitor blood glucose frequently after any alcohol consumption to minimize hypoglycemia risk, with particular vigilance for delayed effects. 3
- Alcohol can cause hypoglycemic unawareness, making recognition of low blood sugar more difficult and potentially dangerous. 5
- Patients should always consume alcohol with food containing carbohydrates to minimize nocturnal hypoglycemia risk. 3
Clinical Implementation Algorithm
Step 1: Patient Assessment
- Confirm alcohol use disorder diagnosis requiring pharmacotherapy for craving reduction. 1, 2
- Assess renal function (creatinine clearance) before initiating acamprosate, as dose adjustment or contraindication applies. 2
- Evaluate current diabetes medications, with special attention to insulin and insulin secretagogues that increase hypoglycemia risk. 3
Step 2: Medication Selection
- Choose naltrexone 50 mg daily as first-line for most diabetes patients due to once-daily dosing and no renal dose adjustment. 1
- Select acamprosate 666 mg three times daily if naltrexone is contraindicated or patient has normal renal function and can adhere to three-times-daily dosing. 2
- Both medications require concurrent comprehensive psychosocial support for optimal efficacy. 1, 2
Step 3: Diabetes Management Optimization
- Intensify glucose monitoring during initial treatment phase, checking before and 2-4 hours after meals, at bedtime, and upon waking. 3
- Consider temporarily raising glycemic targets in patients with frequent hypoglycemia or reduced hypoglycemia awareness. 3
- Educate patients that moderate alcohol consumption (≤1 drink/day for women, ≤2 drinks/day for men) does not have major detrimental effects on long-term glucose control when consumed responsibly with food. 3
Step 4: Safety Education
- Instruct patients to always carry fast-acting glucose sources and wear medical alert identification indicating diabetes. 3
- Teach recognition of hypoglycemia symptoms and appropriate treatment with 15g carbohydrate. 3
- Educate family members about hypoglycemia recognition and glucagon administration if needed. 3
Important Caveats and Pitfalls
Contraindications to Consider
- Absolute abstinence from alcohol is advised for patients with history of alcohol abuse/dependence (which these patients have), pancreatitis, advanced neuropathy, or severe hypertriglyceridemia. 3
- Acamprosate is contraindicated in severe renal impairment, which is more common in diabetes patients with nephropathy. 2
- Monitor for suicidality with acamprosate, as suicidal ideation and attempts occur more frequently than with placebo (2.4% vs 0.8% in year-long studies). 2
Realistic Expectations
- These medications reduce cravings and support abstinence but do not guarantee it—relapse should be anticipated and managed without discontinuing medication. 2
- Naltrexone efficacy was demonstrated in 12-week trials as adjunct to psychosocial methods under conditions enhancing compliance. 1
- Acamprosate should be continued even if patient relapses, as it supports return to abstinence. 2
Glycemic Control Benefits
- Moderate alcohol consumption is inversely associated with HbA1c levels in diabetes patients, with consumption of 1-2.9 drinks/day associated with lower A1c values compared to abstainers. 6
- However, this potential benefit must be weighed against hypoglycemia risk and the primary goal of treating alcohol use disorder. 6
- Chronic excessive alcohol consumption (≥3 drinks/day) causes insulin resistance, pancreatic β-cell dysfunction, and loss of metabolic control. 7