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c/t2dglp1·posted 1 months ago by u/nadia_norgaard

[PSA] hypoglycaemia is not what most of this community thinks it is

Results Well Actually ×2

Writing this once so it can be linked instead of retyped: hypoglycaemia is not what most of this community thinks it is.

Assumed the weight endpoints from the obesity trials applied to my situation. They are different programmes.

Variability dropped before the average did, which was visible on the sensor and invisible on the lab result.

Kept fingersticks alongside the sensor for two weeks to sanity-check it. Worth doing once.

Sceptical readings welcome. The confident ones are the ones I distrust.

1,047 up / 180 down85% upvoted30 commentsid 1tyrm421 Jun 2026

30 comments

25 in this archive, depth 4

best — the order this archive was captured in

u/santiago_rasmussen89 points·1 months ago

Certain conditions affect A1c independently of glycaemia. If a result looks inconsistent with the sensor data, that is a question for whoever manages your care rather than for this board.

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u/cormac_danquah71 points·1 months ago

Disagree — that is an obesity trial endpoint and this thread is about glycaemic control.

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u/a1c_arcT2D19 points·1 months ago

the fasting number is the one people fixate on and it moves last

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[removed]27 points·1 months ago

[removed by moderator]

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u/slow_logbook_notes3032 points·1 months ago

Cosigning that postprandial excursions improve first and the fasting number is the laggard.

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u/sanne_laurent44 points·1 months ago·edited

Push back: one sensor reading is not a data point worth acting on, especially in the first day of wear.

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u/osman_ferrari0 points·1 months ago

Push back: one sensor reading is not a data point worth acting on, especially in the first day of wear.

Disagreeing with this line: that endpoint is from the obesity programme and does not answer the question.

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u/bianca_demir1 point·1 months ago

dose for glycaemic control is not the same conversation as dose for weight

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u/baseline_drifteranalytical18 points·1 months ago

The order things move in, since nobody explains it and it worries people.

Postprandial excursions generally respond earliest. Variability tends to narrow before the average does, which is visible on a sensor and invisible on a lab result. Fasting glucose is often the laggard, and A1c — being a three-month average — is the last thing to reflect anything.

So a month in which the sensor looks better and the fasting number has not moved is the ordinary sequence, not a contradiction. Knowing that in advance would have saved me a quarter of unnecessary worry, which is why it is worth writing down.

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u/fridge_door_no5 points·1 months ago

Small fix — insulin secretion in this class is glucose-dependent, which is precisely why the risk you describe comes from the other agent.

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u/kaia_cabrera4 points·1 months ago

That is a sensor value, not a plasma value, and the two are not interchangeable at that level of precision.

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u/chidi_abubakar26 points·1 months ago

A1c reflects average glycaemia over roughly the preceding three months, weighted towards the most recent weeks. It cannot show variability and it lags any change you make.

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u/bianca_dziedzic7 points·1 months ago

The diabetes and obesity programmes are separate, with different populations and different primary endpoints. Reading a result across from one to the other is not a comparison.

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u/yannick_barros11 points·1 months ago

What does time in range look like, not just the average?

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u/iman_castellanos19 points·1 months ago

Incretin-based agents stimulate insulin secretion in a glucose-dependent manner, which is why hypoglycaemia risk with them alone is low. Risk rises with agents that act independently of glycaemia.

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u/neha_rahimi12 points·1 months ago

Brought the whole CGM export to my appointment rather than one number. Entirely different conversation.

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u/gentle_correctionnice about it10 points·1 months ago

Agreed on variability. Two people with the same average can have completely different days.

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u/tomas_lokken5 points·1 months ago·edited

Correction: that trial is the diabetes programme and the figure you quoted is its glycaemic endpoint, not a weight result.

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u/farid_jansen7 points·1 months ago

Brought the whole CGM export to my appointment rather than one number.

Agreed, and the glucose-dependence point is the reason the risk profile reads the way it does.

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u/arne_amankwah13 points·1 months ago·edited

Continuous monitoring shows the shape: postprandial excursions, overnight behaviour and time in range. Two people with identical A1c can have very different distributions.

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u/niels_salinas4 points·1 months ago

check the trial population before quoting a result at somebody

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u/georgi_haddad8 points·1 months ago

Sensor accuracy varies across wear, and readings on the first day are the least reliable. Calibration practice and compression artefacts explain many alarming single values.

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u/kaia_cabrera4 points·1 months ago

Correcting myself: 18 weeks between those two A1c results, which is too short an interval to interpret.

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u/lyophile_lou1 point·1 months ago

Have you taken this to whoever manages your diabetes?

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u/yannick_barros1 point·1 months ago

Yes — the person managing your diabetes is the one to talk to, and this board is explicit about that.

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Type 2 diabetes as the original indication: A1c trajectories, CGM traces, hypoglycaemia risk when stacked with sulfonylureas or insulin, metformin combinations, and why the weight-loss conversation sometimes drowns out the glycaemic one.

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