Welcome! đIâm Dr. Susan Brian, a board-certified endocrinologist, certified menopause specialist, and clinical researcher with over 18 post Fellowship ďżźyears of experience helping women navigate the complex changes that come with hormones, metabolism, weight, and aging.
On this channel, youâll find evidence-based information about menopause, perimenopause, GLP-1 medications, obesity medicine, thyroid disease, PMOS, bone health, insulin resistance, and healthy aging â explained in a way that makes sense without the medical jargon.
As an active clinical researcher involved in studies of emerging obesity and metabolic therapies, I share the latest science, clinical trial updates, and what new discoveries may mean for real patients and real lives.
The information shared on this channel is for educational purposes only and is not personal medical advice. Please discuss your individual medical care with your healthcare professional.
Susan Brian MD
Have you heard of Zenagamtide yet?
It has been called âamycretinâ until now.
Itâs an investigational dual GLP-1/amylin receptor agonist from Novo in research currently for obesity and type 2 diabetes.
Itâs different than CagriSema (I think will likely be approved in 2027), which combines two separate drugs, zenagamtide is a single molecule designed to activate both pathways.
Early trials have shown significant weight lossâ 24% at 36 weeks âalthough this was a small early-phase study (larger Phase 3 trials now underway)
It is also being developed as an oral medication.
The most common side effects so far are gastrointestinal, similar to other incretin-based drugs, and it is not yet FDA-approved
1 week ago | [YT] | 9
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Susan Brian MD
Sobel TH, Shen W. Menopause. 2022;29(4):483â490. doi:10.1097/GME.0000000000001938.
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Susan Brian MD
Insulin resistance is often talked about as if it has one clear symptom or a single blood test that can diagnose it, but itâs more complex than that.
Insulin resistance is a physiologic state where the body needs more insulin than normal to keep blood sugar in a healthy range. Because of this, a person can have insulin resistance for years before developing prediabetes or type 2 diabetes.
Certain physical and metabolic signs can raise suspicion, including acanthosis nigricans (darkened skin patches), increased abdominal fat, high blood pressure, high triglycerides, low HDL cholesterol, MASLD (fatty liver disease), and PCOS. However, none of these findings alone is enough to make a diagnosis.
In research and some clinical settings, insulin resistance can be estimated using HOMA-IR (Homeostatic Model Assessment of Insulin Resistance). This is calculated from fasting blood tests: fasting insulin (ÂľU/mL) Ă fasting glucose (mg/dL) á 405. In general, higher values suggest greater insulin resistance. However, there is no single agreed-upon cutoff that defines insulin resistance. Different studies use different thresholds, and values around 2.0â2.5 are sometimes used in research, but these should not be treated as a universal diagnostic standard.
HOMA-IR does correlate reasonably well with more precise methods, such as the glucose clamp technique, when looking at large groups of people. However, it is not commonly used in routine medical care to diagnose insulin resistance, mainly because insulin testing is not standardized across laboratories and there is no consistent clinical cutoff.
Itâs also important to understand that the percentage of people labeled as having âelevatedâ HOMA-IR varies widely. It depends entirely on the cutoff used and the population being studied, so there is no single fixed prevalence.
Current guidelines, including the 2026 ADA Standards of Care, recommend using established tests such as A1C, fasting plasma glucose, or an oral glucose tolerance test to screen for prediabetes and type 2 diabetes, rather than relying on HOMA-IR.
Overall, the key message is that metabolic risk can be identified early. We do not need to wait for diabetes to develop before recognizing or addressing insulin resistance.
1 week ago | [YT] | 0
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Susan Brian MD
Iâm pretty excited about the possibility of CagriSema getting FDA approval.
Did you see the new study?
The phase 3a REIMAGINE 3 trial was just published in The Lancet (July 2026)â it evaluated once-weekly cagrilintideâsemaglutide (CagriSema) as an add-on to basal insulin in 274 adults with type 2 diabetes and lasted 40 weeks. (this medicine hasnât been FDA approved yet)
The A1c reduction was very impressive!
Both the 2.4 mg and 1.0 mg doses produced substantially greater HbA1c reductions than placebo (â2.33% and â2.10% vs. â0.66%), while also helping with significant weight loss.
ALSO***What makes these findings really interesting is that these improvements were achieved without increasing the risk of hypoglycemia, despite participants remaining on basal insulinâa common concern whenever any medicine is added to insulin (we counsel our patients about lowering the insulin appropriately )
CagriSema looks like it might become a great option for people with type 2 diabetes on basal insulin but still struggling to reach glycemic and weight-management goals.
3 weeks ago | [YT] | 0
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Susan Brian MD
Thanks to Dr Hollie Wakelyn, PharmD for her help with this chart - use it to help change between estrogen doses while there is a patch shortage!
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Susan Brian MD
I think you might have to tap on the image to see the full text? Let me know if you have any questions below!âŹď¸
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