Preferential Maternal Transmission of STX16‐GNAS Mutations Responsible for Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B): Another Example of Transmission Ratio Distortion. (27th December 2020)

• Record Type: Journal Article
• Authors: Kiuchi, Zentaro; Reyes, Monica; Jüppner, Harald
• Is Part Of: Journal of bone and mineral research. Volume 36:Number 4(2021)
• Page Start: 696
• Page End: 703
• Publication Date: 2020-12-27
• Subjects: PHP1A -- TRANSMISSION RATIO DISTORTION -- PARATHYROID HORMONE -- EPIGENETICS; Bones -- Metabolism -- Periodicals; Mineral metabolism -- Periodicals; 612.392
• DOI: 10.1002/jbmr.4221
• Languages: English
• ISSNs: 0884-0431

Abstract

ABSTRACT: Preferential transmission of a genetic mutation to the next generation, referred to as transmission ratio distortion (TRD), is well established for several dominant disorders, but underlying mechanisms remain undefined. Recently, TRD was reported for patients affected by pseudohypoparathyroidism type Ia or pseudopseudohypoparathyroidism. To determine whether TRD is observed also for autosomal dominant pseudohypoparathyroidism type Ib (AD‐PHP1B), we analyzed kindreds with the frequent 3‐kb STX16 deletion or other STX16/GNAS mutations. If inherited from a female, these genetic defects lead to loss‐of‐methylation at exon A/B alone or at all three differentially methylated regions (DMR), resulting in parathyroid hormone (PTH)‐resistant hypocalcemia and hyperphosphatemia and possibly resistance to other hormones. In total, we investigated 212 children born to 80 females who are unaffected carriers of a STX16/GNAS mutation ( n = 47) or affected by PHP1B ( n = 33). Of these offspring, 134 (63.2%) had inherited the genetic defect ( p = .00012). TRD was indistinguishable for mothers with a STX16/GNAS mutation on their paternal (unaffected carriers) or maternal allele (affected). The mechanisms favoring transmission of the mutant allele remain undefined but are likely to include abnormalities in oocyte maturation. Search for mutations in available descendants of males revealed marginally significant evidence for TRD ( p = .038), but these analyses are less reliable because many more offspring of males than females with a STX16/GNAS mutation were lost to follow‐up (31 of 98 versus 6 of 218). This difference in follow‐up is probably related to the fact that inheritance of a mutation from a male does not have clinical implications, whereas inheritance from an affected or unaffected female results in PHP1B. Lastly, affected PHP1B females had fewer descendants than unaffected carriers, but it remains unclear whether abnormal oocyte development or impaired actions of reproductive hormones are responsible. Our findings highlight previously not recognized aspects of AD‐PHP1B that are likely to have implications for genetic testing and counseling. © 2020 American Society for Bone and Mineral Research (ASBMR).