Clinical disclaimer: This article is educational and does not constitute personal medical advice. If you take medication affected by weight change, or have type 2 diabetes, involve your clinician before making any changes. Never stop medication abruptly without clinical supervision.

Why blood tests before stopping matter

Stopping GLP-1 medication is not just about appetite and weight. These drugs affect glucose metabolism, blood pressure, lipids, kidney function, and liver enzymes. A blood test snapshot before stopping gives you a baseline against which to measure change — and may reveal findings that alter whether or when you stop, or what monitoring you need after.

The right panel depends on your indication, comorbidities, and medication list. There is no universal pre-stopping blood test requirement — but there are tests that are clinically useful for most people and essential for some.

HbA1c: essential if you have diabetes or pre-diabetes

GLP-1 agents lower HbA1c through multiple mechanisms. Stopping will worsen glucose control to some degree in anyone with impaired glucose metabolism. Knowing your HbA1c before stopping gives your clinician the information to decide whether additional glucose management is needed and sets a baseline for monitoring in the weeks after. If your HbA1c is well-controlled on GLP-1 medication, stopping without an alternative glucose plan in place is clinically incomplete. [1]

If you have pre-diabetes rather than established type 2 diabetes, the HbA1c still matters — weight gain after stopping may push glucose back toward the diabetic threshold.

Fasting lipids: often overlooked but important

GLP-1-assisted weight loss typically improves lipid profiles — LDL, triglycerides, and HDL all tend to move favourably. [2] These gains reverse with weight regain. A lipid panel before stopping records where you are while the medication is working — if stopping leads to significant weight regain and lipid deterioration, having a pre-stopping baseline means the deterioration is visible and actionable rather than ambiguous.

This is particularly relevant if cardiovascular risk is part of the clinical picture, or if lipid-lowering medication was reviewed (reduced or stopped) during the weight loss phase.

Kidney function: eGFR and creatinine

GLP-1 agents have been shown to have renoprotective effects in patients with chronic kidney disease (the FLOW trial demonstrated this for semaglutide). [3] In patients with established kidney disease, stopping GLP-1 medication removes this protection. Knowing current eGFR and creatinine before stopping allows monitoring of any kidney function change after cessation — which in a patient with CKD may be clinically significant.

For most patients without known kidney disease, a baseline creatinine is useful principally to rule out occult impairment that might affect other medication choices.

Liver enzymes: ALT and AST

GLP-1 agents improve metabolic dysfunction-associated steatohepatitis (MASH) and generally reduce liver enzymes in patients with fatty liver disease. [4] If you have elevated liver enzymes at baseline and these improved during GLP-1 treatment, a pre-stopping measurement records the improvement. Reversal after stopping — if weight is regained — is predictable and worth tracking.

What blood tests alone cannot tell you

Blood tests are a snapshot, not a monitoring system. The most important pre-stopping assessment for most patients is blood pressure — checked sitting and standing, not just at a single point. This is particularly true if you are on antihypertensives, where the consequences of getting the medication adjustment wrong are immediate (dizziness, falls) rather than deferred (as with lipids or HbA1c). Read more in blood pressure after weight loss.

A Clinical Data Review interprets your existing results in the context of your medication list and stopping plan — it does not require starting from scratch.

Timing: when to test

Ideally, blood tests before stopping should be taken while the medication is still active — reflecting the best metabolic state — not the day before the last dose when levels are near a trough. This gives the clearest picture of what the medication achieved and what is at risk of reversing. Allow four to eight weeks after stopping before repeating, which gives enough time for meaningful change to show.

FAQ

What blood tests should I have before stopping Mounjaro?
The core panel for most people: HbA1c if you have diabetes or pre-diabetes; fasting lipids; eGFR and creatinine; and liver enzymes (ALT, AST) if you had fatty liver disease at baseline. Blood pressure is as important as any blood test. The specific panel depends on your indication and comorbidities.
Do I need blood tests before stopping Wegovy?
Not mandatorily, but they are clinically useful. The most important are HbA1c if your glucose metabolism is impaired, lipids if cardiovascular risk is relevant, and kidney function if there is any known kidney disease. If none of these apply, blood pressure monitoring is the more important pre-stopping step.
How soon after stopping GLP-1 medication should I repeat blood tests?
Allow four to eight weeks before repeating, which gives enough time for meaningful metabolic change to show. HbA1c reflects a three-month average — a repeat at six weeks captures early deterioration, not the full picture. Lipids can change within four weeks of weight change.
Will my cholesterol go up after stopping Mounjaro?
Likely, if weight is regained. GLP-1-assisted weight loss typically improves LDL, triglycerides, and HDL. These improvements reverse with weight regain. The rate and degree depend on how much weight is regained and how quickly.
Can I get a Clinical Data Review from Dr Dan Reardon?
Yes. A Clinical Data Review interprets your existing blood test and wearable data in the context of your medication and stopping plan. It does not require new tests — it works with what you already have.

References

  1. NICE. Type 2 diabetes in adults: management. NG28. 2024.
  2. Aronne LJ et al. Cardiometabolic parameter change by weight regain on tirzepatide withdrawal: SURMOUNT-4 post hoc analysis. JAMA Intern Med. 2025.
  3. Perkovic V et al. Semaglutide and kidney outcomes in type 2 diabetes. FLOW trial. N Engl J Med. 2024.
  4. Newsome PN et al. A placebo-controlled trial of subcutaneous semaglutide in nonalcoholic steatohepatitis. NASH trial. N Engl J Med. 2021.