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ð äžé éé»
- 22E: GPCR biased agonism, allosteric modulators, gene therapy for hormone resistance, AAV approaches
- Taiwan: å¥ä¿ IGF-1 (mecasermin), GH replacement, GnRH agonist æè·è
º/åå®®å
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ð Pearls (12)
- Biased agonism: GPCR can preferentially signal through G-protein vs β-arrestin
- Allosteric modulators: cinacalcet (CaSR PAM, hyperparathyroidism)
- Setmelanotide for MC4R pathway obesity (BBS, POMC, LEPR)
- Mecasermin (rhIGF-1) for severe primary IGF-1 deficiency / Laron
- β-arrestin biased TRH in trials
- PROTAC targeting nuclear receptors (estrogen receptor degrader)
- Selective glucocorticoid receptor modulators (SEGRMs) in trials
- THRβ-specific agonist (resmetirom) for NASH
- PPAR pan-agonist for diabetes/dyslipidemia
- CRISPR therapy for genetic endocrine disorders (in trials)
- Continuous SC pump for replacement (cortisol pump trials)
- Bioidentical vs synthetic hormone considerations
ð Taiwan + å¥ä¿
- å¥ä¿ GH replacement (somatropin) for adult/peds GHD
- å¥ä¿ mecasermin for Laron / severe IGF-1 deficiency éå¶
- å¥ä¿ GnRH agonist (leuprolide, goserelin) æè·è
º/åå®®å
§èç°äœ
- å¥ä¿ GnRH antagonist (degarelix) æè·è
º
- å¥ä¿ cinacalcet å¯ç²çè
ºäº¢é² (CKD/parathyroid CA)
- å¥ä¿ setmelanotide éå¶ïŒçœç
ïŒ
ð å
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æ
- Receptor é¡å¥ + ä¿¡èè·¯åŸ
- Carrier proteins
- Activating vs inactivating mutations ç¯äŸ
- McCune-Albright spectrum
- Pulsatile / circadian åè¡ææ©
- Resistance syndromes
- 22E: biased agonism, SEGRM, PROTAC, gene therapy
- Taiwan: å¥ä¿ GH/IGF-1/GnRH agonist æ¢ä»¶
â ïž AI èçš¿ã