الجمعية العربية لتداخلات الغدد الصماء و تكنولوجيا السكر

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الجمعية العربية لتداخلات الغدد الصماء و تكنولوجيا السكر الجمعية العربية لتداخلات الغدد الصماء و تكنولوجيا السكر (PASID)

09/06/2026

هل هناك علاقة بين السكري والغدة الدرقية؟
هل تعلم أن هناك رابطاً قوياً بين مرض السكري وصحة الغدة الدرقية؟ تشير الدراسات الحديثة في مصر إلى أن حوالي واحد من كل أربعة مصابين بالسكري قد يعاني أيضاً من اضطراب في الغدة الدرقية. الغدة الدرقية هي "المحرك" الصغير الموجود في رقبتك والذي يتحكم في طاقة جسمك وحرق الغذاء. أحياناً، يؤثر السكري على هذا المحرك ويجعله يعمل ببطء، وهو ما يسمى "خمول الغدة" . الخبر الجيد هو أن اكتشاف هذا الخلل مبكراً يساعدك كثيراً في التحكم بمستويات السكر ويحميك من التعب والإرهاق غير المبرر. صحتك غالية، والوعي هو أول خطوة لحمايتها.

نصيحة اليوم: في زيارتك القادمة للطبيب، اسأله عن فحص الغدة الدرقية (TSH) للاطمئنان على محرك جسمك!

#السكري

New Clinical Update for Healthcare ProfessionalsExplore the latest American Thyroid Assossication 2026 Guidelines addres...
09/06/2026

New Clinical Update for Healthcare Professionals

Explore the latest American Thyroid Assossication 2026 Guidelines addressing thyroid disease management during preconception, pregnancy, and the postpartum period.

Key evidence-based recommendations supporting optimal maternal and fetal outcomes.
Below is one of the most prominent
highlights of your clinical practice

Postpartum Recovery and Transitions
Postpartum thyroiditis (PPT) is common and often transient; its thyrotoxic phase should be managed with beta-blockers rather than antithyroid drugs. For patients who started levothyroxine during pregnancy for mild dysfunction, the guidelines recommend a standardized cessation trial after delivery to avoid lifelong unnecessary medication. Continuous monitoring remains vital, as many women with PPT eventually progress to permanent hypothyroidism.
Takeaway: Don't let gestational therapy become permanent by default—schedule a postpartum re-evaluation at six weeks.

’sHealth

PASID & American Diabetes Association  2026 | Breaking News 🚨🚨🚨Beyond GLP-1: The New Race in Obesity, Diabetes & Metabol...
09/06/2026

PASID & American Diabetes Association 2026 | Breaking News 🚨🚨🚨

Beyond GLP-1: The New Race in Obesity, Diabetes & Metabolic Liver Disease

ADA 2026 is making one thing very clear:

The future of metabolic medicine is no longer about GLP-1 alone.

We are now entering the era of:

-Dual agonists
-Triple agonists
-Amylin-based combinations
-Oral small-molecule GLP-1 therapies
-Liver-targeted obesity treatments

Here are four major programs to watch closely:

1. Survodutide — Boehringer Ingelheim / Zealand Pharma
Mechanism: Dual glucagon/GLP-1 receptor agonist
Key trials: SYNCHRONIZE-1 and SYNCHRONIZE-MASLD

Survodutide is particularly exciting because it is not only a weight-loss therapy; it may also become a major player in MASLD/MASH, where obesity, diabetes, insulin resistance, and liver disease overlap.

In SYNCHRONIZE-1, survodutide achieved significant weight loss in people with obesity or overweight without diabetes, with reported mean weight loss up to 16.6% after 76 weeks.

The liver angle is what makes this drug different. With the rapid rise of MASLD and MASH, the next generation of obesity therapies may be judged not only by weight reduction, but also by liver fat reduction, inflammation, fibrosis signals, and long-term cardiometabolic protection.

2. CagriSema — Novo Nordisk

Mechanism: Cagrilintide + semaglutide
Class: Amylin analogue + GLP-1 receptor agonist
Key trials: REIMAGINE-1, REIMAGINE-2, REIMAGINE-3

In REIMAGINE-2, once-weekly CagriSema showed HbA1c reduction of 1.91 percentage points and body-weight reduction of 14.2% in adults with type 2 diabetes, outperforming semaglutide alone in that trial.

3. Orforglipron — Eli Lilly
Mechanism: Oral non-peptide GLP-1 receptor agonist
Brand name: Foundayo
Key trials: ACHIEVE program

Orforglipron may represent one of the most practical breakthroughs in the field: an oral GLP-1 tablet without the complex fasting, water, and timing restrictions required with oral semaglutide.

The ACHIEVE program includes comparisons with:
-Dapagliflozin — ACHIEVE-2
-Oral semaglutide — ACHIEVE-3
-Placebo added to insulin glargine — ACHIEVE-5

Lilly reported that phase 3 ACHIEVE results showed orforglipron outperformed oral semaglutide and dapagliflozin in type 2 diabetes, supporting its potential to redefine oral incretin therapy.

4. AZD5004 / Elecoglipron — AstraZeneca / Eccogene
Mechanism: Oral small-molecule GLP-1 receptor agonist
Key trials: VISTA and SOLSTICE

The VISTA trial evaluates the drug in overweight/obesity, while SOLSTICE evaluates it in type 2 diabetes. SOLSTICE is a phase 2b randomized, double-blind, placebo-controlled study in adults with T2D.

This is important because the oral GLP-1 space is becoming highly competitive, and the next big disruption may not be “more weight loss” alone, but easier delivery, better scalability, and improved access.

New Clinical Update for Healthcare ProfessionalsExplore the latest American Thyroid Assossication 2026 Guidelines addres...
08/06/2026

New Clinical Update for Healthcare Professionals

Explore the latest American Thyroid Assossication 2026 Guidelines addressing thyroid disease management during preconception, pregnancy, and the postpartum period.

Key evidence-based recommendations supporting optimal maternal and fetal outcomes.
Below is one of the most prominent
highlights of your clinical practice

Navigating Hyperthyroidism and Graves'
Clinicians must distinguish self-limiting gestational transient thyrotoxicosis (GTT) from Graves' disease using TRAb/TSI titers, as GTT requires only supportive care. If antithyroid drugs are necessary, propylthiouracil (PTU) is the preferred agent during the first trimester to minimize the risk of severe congenital malformations associated with methimazole. Any mother on these medications or with high antibody titers requires fetal ultrasound monitoring starting at 18–20 weeks.
Takeaway: Switch Graves' patients to PTU before conception or as soon as pregnancy is confirmed.

’sHealth

New Clinical Update for Healthcare ProfessionalsExplore the latest American Thyroid Assossication 2026 Guidelines addres...
07/06/2026

New Clinical Update for Healthcare Professionals

Explore the latest American Thyroid Assossication 2026 Guidelines addressing thyroid disease management during preconception, pregnancy, and the postpartum period.

Key evidence-based recommendations supporting optimal maternal and fetal outcomes.
Below is one of the most prominent
highlights of your clinical practice

Precision in Gestational Hypothyroidism

The indication for treating subclinical hypothyroidism is now heavily influenced by gestational age. Evidence suggests that levothyroxine benefits are primarily seen when treatment starts in the first trimester; treatment initiated later in pregnancy may not improve neurocognitive or obstetric outcomes. For overt hypothyroidism (TSH ≥ 6 mU/L or persistent elevation), monotherapy with levothyroxine is mandatory, while combination therapies (T3/desiccated thyroid) are strictly discouraged due to fetal brain requirements.
Takeaway: The first trimester is the most critical window—act early to maximize potential neurodevelopmental benefits.

’sHealth

PASID & American Diabetes Association  2026 | Breaking News 🚨🚨🚨Retatrutide: Is This the Closest We Have Ever Come to Bar...
07/06/2026

PASID & American Diabetes Association 2026 | Breaking News 🚨🚨🚨

Retatrutide: Is This the Closest We Have Ever Come to Bariatric Surgery Without Surgery?

One of the biggest stories at ADA 2026 is undoubtedly Retatrutide, Eli Lilly’s next-generation triple hormone receptor agonist that simultaneously targets:
1-GLP-1 receptor
2-GIP receptor
3-Glucagon receptor

This unique “Triple-G” mechanism not only reduces appetite and food intake but may also increase energy expenditure, helping explain the unprecedented weight-loss results being reported.

What is New at ADA 2026?

(A)TRIUMPH-1 (Phase 3 Obesity Trial)
In adults with obesity or overweight without diabetes:
-28.3% average weight loss with the 12 mg weekly dose at 80 weeks
-Average weight reduction of 70.3 lbs (31.9 kg)
-45.3% of participants achieved ≥30% weight loss
-More than 85% achieved ≥15% weight loss
-Nearly all participants lost at least 5% of body weight

🤩Participants in the extension study reached 30.3% average weight loss at 104 weeks (~85 lbs / 38.5 kg)

👌👌Beyond Weight Loss; Retatrutide demonstrated clinically meaningful improvements in multiple obesity-related conditions:
-Obstructive Sleep Apnea (OSA)
-Knee Osteoarthritis symptoms
-Blood pressure reduction
-Lipid profile improvement
-Prediabetes remission to normoglycemia in >95% of participants

(B) TRANSCEND-T2D-1 (Phase 3 Diabetes Trial)
In adults with Type 2 Diabetes: Baseline HbA1c: 7.9%

At Week 40:
👉HbA1c reduction of 1.7–2.0%
👉HbA1c levels reached approximately 5.9–6.2%
👉Weight loss up to 16.8%
👉No weight-loss plateau observed
👉Continued downward weight trajectory throughout the study period

The most common adverse events were typical incretin-related GIT effects: Nausea, Vomiting, Diarrhea &Constipation
Most events were mild to moderate and occurred during dose escalation.

A unique finding seen more frequently with higher doses was dysesthesia (abnormal skin sensations), which appears to be a distinguishing feature of retatrutide compared with currently available GLP-1 therapies.

Today, for the first time, a medication is producing:
😳 ~30% body weight reduction
😳Nearly half of patients losing ≥30% of body weight
😳Significant metabolic improvements
😳Major benefits across obesity-related complications

These results are approaching outcomes historically associated with metabolic surgery.

A few years ago, we asked: ((Can medications reach 15% weight loss?)), Today, the question has become: (((Can medications replace bariatric surgery for many patients?)))

Retatrutide may be the strongest evidence yet that the answer could be yes for selected patients.

📍 This is the second post in the PASID ADA 2026 Highlights Series.

Follow PASID for daily updates from ADA 2026 on obesity, diabetes, AI, CGM, cardiovascular outcomes, and next-generation therapies.

06/06/2026

خبر سار لكل من يعاني من السكري من النوع الثاني وزيادة الوزن! 🌟

هل تتخيلون أن العلاج قد يصبح حقنة واحدة فقط كل شهر بدلاً من كل أسبوع؟ الدراسات الحديثة كشفت عن دواء جديد واعد يسمى "بيروبيناتيد" (Berobenatide). هذا الدواء مصمم ليكون طويل المفعول جداً، حيث يعمل على تنظيم مستويات السكر في الدم ومساعدة الجسم على فقدان الوزن الزائد بفعالية كبيرة .

أظهرت النتائج أن هذا العلاج ساعد المرضى على تقليل نسبة السكر التراكمي بشكل ملحوظ، مع تحقيق نقص واضح في الوزن وصل إلى أكثر من 10% خلال أشهر قليلة. الأهم من ذلك هو الراحة؛ فبدلاً من الالتزام بحقن أسبوعية، تمنحكم هذه التقنية حرية أكبر ووخزات أقل، مما يسهل عليكم الالتزام بالعلاج والاستمرار في حياتكم بنشاط.

بالنسبة للأعراض، فقد كانت بسيطة وغالباً ما تقتصر على شعور خفيف بلعيان النفس يزول مع الوقت. نحن دائماً نشجعكم على استشارة طبيبكم المختص لمناقشة أحدث الخيارات العلاجية التي تناسب حالتكم، ولا تنسوا أن الخطوات الصغيرة في تنظيم الغذاء والحركة تصنع فرقاً كبيراً في صحتكم. 💙

ما هو رأيكم؟ هل تجدون أن العلاج الشهري سيغير من روتينكم اليومي للأفضل؟

#صحة #سكري #السمنة

PASID & American Diabetes Association  2026 | Breaking News 🚨🚨🚨What if the future of obesity and type 2 diabetes treatme...
06/06/2026

PASID & American Diabetes Association 2026 | Breaking News 🚨🚨🚨

What if the future of obesity and type 2 diabetes treatment is not a weekly injection… but a once-monthly injection?

One of the most talked-about presentations at ADA 2026 was Berobenatide (PF-08653944), Pfizer’s ultra-long-acting GLP-1 receptor agonist designed to potentially enable monthly dosing while maintaining the powerful metabolic benefits we expect from modern incretin therapies.

Key Results from VESPER-2

(Adults with Type 2 Diabetes and Obesity/Overweight)

At just 28 weeks:

-HbA1c reduction of up to 2.2%
-Body weight reduction of up to 10.2%
-Gastrointestinal adverse events were predominantly mild or moderate
-No meaningful signal of severe nausea
-Safety profile consistent with the established GLP-1 receptor agonist class

Why Is This Important?
The next major battle in obesity medicine may not be about achieving greater weight loss alone.

It may be about:
👌Fewer injections
👌Better treatment adherence
👌Improved patient convenience
👌Long-term persistence on therapy

Berobenatide is being developed as an ultra-long-acting GLP-1 RA, with studies exploring maintenance regimens as infrequent as once monthly, potentially redefining how patients receive obesity and diabetes therapies.

Monthly Dosing Strategy
The VESPER program evaluated transition strategies from weekly dosing to long-acting maintenance regimens, including:
3.2 mg monthly and 4.8 mg monthly

Importantly, weight reduction continued after transitioning to monthly administration, suggesting sustained biological activity despite less frequent injections.

VESPER-1 Extension Study
(Adults with Obesity/Overweight without Diabetes)
👏Up to 16% weight loss was achieved with weekly berobenatide at 32 weeks.
👏Weight loss continued through Week 60.
👏No severe gastrointestinal adverse events were reported in the open-label extension.

What Happens Next?
The encouraging Phase 2 data have supported the ongoing global Phase 3 VESPER program, positioning berobenatide as one of the most promising next-generation GLP-1 therapies currently in development.

📍 This is the first post in the PASID ADA 2026 Highlights Series.

Over the coming days, we will bring you the most important ADA 2026 updates in:
👉Obesity Medicine
👉Type 2 Diabetes
👉 CGM & Diabetes Technology
👉 Artificial Intelligence in Healthcare
👉 Cardiovascular & Kidney Outcomes
👉 Emerging Therapies

Follow PASID for daily scientific highlights from ADA 2026.

New Clinical Update for Healthcare ProfessionalsExplore the latest American Thyroid Association 2026 Guidelines addressi...
06/06/2026

New Clinical Update for Healthcare Professionals

Explore the latest American Thyroid Association 2026 Guidelines addressing thyroid disease management during preconception, pregnancy, and the postpartum period.

Key evidence-based recommendations supporting optimal maternal and fetal outcomes.
Below is one of the most prominent
highlights of your clinical practice .

Paradigm Shift in Infertility Management
For women with infertility or recurrent miscarriage, the target TSH remains 0.5–2.5 mU/L during treatment. However, high-quality trials have led to a major change: levothyroxine should no longer be offered to euthyroid women who are TPOAb positive, as it does not improve live birth rates. Furthermore, because mild TSH elevations often spontaneously normalize, diagnostic confirmation with repeat testing is recommended before starting therapy.
Takeaway: Reserve levothyroxine for confirmed hypothyroidism and stop treating euthyroid "antibody-only" cases.

’sHealth

05/06/2026

هل تخططين لاستقبال فرد جديد في عائلتك أو أنتِ في رحلة الحمل بالفعل؟
صحتك هي الأساس الذي يبني مستقبل طفلك الصغير. الغدة الدرقية، تلك الغدة الصغيرة في رقبتك، تعمل كـ "محرك" ينظم نمو طفلك وتطور دماغه بشكل سليم.

لكي يعمل هذا المحرك بكفاءة، يحتاج إلى "وقود" أساسي وهو اليود. التوصيات الطبية الحديثة لعام 2026 تؤكد أن الحصول على كمية كافية من اليود (حوالي 250 ميكروجرام يومياً) أمر ضروري جداً للأم والجنين. يمكنك العثور على هذا العنصر الهام في أطعمة بسيطة نأكلها يومياً مثل لأسماك (كالسلمون)، البيض، ومنتجات الألبان.

تذكري أن جسمك يمر بتغيرات مذهلة خلال الحمل، ومن الطبيعي أن تزداد احتياجاتك الغذائية لتغطية متطلبات طفلك . إذا شعرتِ بخمول غير معتاد أو رغبتِ في الاطمئنان، فإن فحصاً بسيطاً لمستوى الهرمونات قد يمنحك الراحة النفسية اللازمة.

صحتك وصحة طفلك تستحق الاهتمام؛ ابدئي باعتماد غذاء متوازن اليوم، ولا تترددي في استشارة طبيبك للاطمئنان على وظائف الغدة الدرقية لضمان رحلة حمل آمنة وسعيدة.




#اليود







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