A Pharmacogenetic Approach to the Treatment of Patients With PPARG Mutations

作者：Agostini Maura; Schoenmakers Erik; Beig Junaid; Fairall Louise; Szatmari Istvan; Rajanayagam Odelia; Muskett Frederick W; Adams Claire; Marais A David; O'Rahilly Stephen; Semple Robert K; Nagy Laszlo; Majithia Amit R; Schwabe John W R; Blom Dirk J; Murphy Rinki; Chatterjee Krishna; Savage David B

来源：Diabetes, 2018, 67(6): 1086-1092.

DOI：10.2337/db17-1236

Loss-of-function mutations in PPARG cause familial partial lipodystrophy type 3 (FPLD3) and severe metabolic disease in many patients. Missensemutations in PPARG are present in similar to 1 in 500 people. Although mutations are often binarily classified as benign or deleterious, prospective functional classification of all missense PPARG variants suggests that their impact is graded. Furthermore, in testing novel mutations with both prototypic endogenous (e.g., prostaglandin J2 [PGJ2]) and synthetic ligands (thiazolidinediones, tyrosine agonists), we observed that synthetic agonists selectively rescue function of some peroxisome proliferator-activated receptor-gamma (PPAR gamma) mutants. We report on patients with FPLD3 who harbor two such PPAR gamma mutations (R308P and A261E). Both PPAR gamma mutants exhibit negligible constitutive or PGJ2-induced transcriptional activity but respond readily to synthetic agonists in vitro, with structural modeling providing a basis for such differential ligand-dependent responsiveness. Concordant with this finding, dramatic clinical improvement was seen after pioglitazone treatment of a patient with R308P mutant PPAR gamma. A patient with A261E mutant PPAR gamma also responded beneficially to rosiglitazone, although cardiomyopathy precluded prolonged thiazolidinedione use. These observations indicate that detailed structural and functional classification can be used to inform therapeutic decisions in patients with PPARG mutations.

• 出版日期2018-6