Literature DB >> 35749012

Pituitary stalk interruption syndrome: phenotype, predictors, and pathophysiology of perinatal events.

Chakra Diwaker1, Puja Thadani2, Saba Samad Memon1, Vijaya Sarathi3, Anurag Ranjan Lila1, Sneha Arya1, Brijesh Krishnappa1, Manjiri Karlekar1, Virendra A Patil1, Nalini Shah1, Tushar Bandgar4.   

Abstract

PURPOSE: There is limited data regarding Pituitary Stalk Interruption Syndrome (PSIS) from India. Moreover, the pathophysiological link between perinatal events and PSIS is unclear. We aim to elucidate the predictors of PSIS among patients with growth hormone deficiency (GHD) and perinatal events in PSIS by comparing cohorts of PSIS and genetically proven GHD without PSIS.
METHODS: Among 179 GHD patients, 56 PSIS and 70 genetically positive GHD (52-GHRHR, 15-POU1F1, and 3-PROP1) patients were included. Perinatal events, clinical anomalies, pituitary hormone deficiency, and imaging findings were recorded. We compared PSIS-isolated GHD (PSIS-IGHD) subgroup with GHRHR-IGHD and PSIS-combined pituitary hormone deficiency (PSIS-CPHD) subgroup with POU1F1/PROP1-CPHD.
RESULTS: PSIS patients (45 males, median age: 12.5 years) most commonly presented with short stature. At last follow-up (median age: 17.35 years), gonadal (during pubertal-age), thyroid and cortisol axes were affected in 81.6%, 62.5%, and 62.5%. 10/13 (77%) of PSIS children with initial IGHD diagnosis manifested hypogonadism during pubertal age. Male predominance, sporadic presentation, and clinical anomalies were significantly higher in both PSIS subgroups than in the respective genetic subgroups. Breech presentation was higher in PSIS-CPHD than POU1F1/PROP1-CPHD (44.4% vs 5.5%, p = 0.004). Neonatal hypoglycemia (22% vs. 0%, p = 0.05) and jaundice (42 vs. 5%, p = 0.004) were higher in PSIS-CPHD than PSIS-IGHD.
CONCLUSION: Later age at presentation and frequent hypogonadism were observed in our PSIS cohort. Male sex, sporadic presentation, clinical anomalies, and breech presentation predicted PSIS at presentation. Breech presentation in PSIS is likely due to stalk interruption rather than hormonal deficiency.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Breech presentation; Ectopic posterior pituitary; Extra pituitary malformation; Pituitary stalk interruption syndrome

Mesh:

Substances:

Year:  2022        PMID: 35749012     DOI: 10.1007/s11102-022-01243-x

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   3.599


  22 in total

1.  Pituitary stalk interruption syndrome: a clinical-biological-genetic assessment of its pathogenesis.

Authors:  G Pinto; I Netchine; M L Sobrier; F Brunelle; J C Souberbielle; R Brauner
Journal:  J Clin Endocrinol Metab       Date:  1997-10       Impact factor: 5.958

Review 2.  DIAGNOSIS OF ENDOCRINE DISEASE: Pituitary stalk interruption syndrome: etiology and clinical manifestations.

Authors:  Julia Vergier; Frederic Castinetti; Alexandru Saveanu; Nadine Girard; Thierry Brue; Rachel Reynaud
Journal:  Eur J Endocrinol       Date:  2019-11       Impact factor: 6.664

3.  Clues for Polygenic Inheritance of Pituitary Stalk Interruption Syndrome From Exome Sequencing in 20 Patients.

Authors:  Nitash Zwaveling-Soonawala; Marielle Alders; Aldo Jongejan; Lidija Kovacic; Floor A Duijkers; Saskia M Maas; Eric Fliers; A S Paul van Trotsenburg; Raoul C Hennekam
Journal:  J Clin Endocrinol Metab       Date:  2018-02-01       Impact factor: 5.958

4.  Ectopic posterior pituitary and stalk abnormality predicts severity and coexisting hormone deficiencies in patients with congenital growth hormone deficiency.

Authors:  Varsha S Jagtap; Shrikrishna V Acharya; Vijaya Sarathi; Anurag R Lila; Sweta R Budyal; Rajeev Kasaliwal; Shilpa S Sankhe; Tushar R Bandgar; Padmavathy S Menon; Nalini S Shah
Journal:  Pituitary       Date:  2012-06       Impact factor: 4.107

5.  Congenital hypopituitarism: clinico-radiological correlation.

Authors:  Pinaki Dutta; Anil Bhansali; Paramjeet Singh; Rajesh Rajput; Niranjan Khandelwal; Sanjay Bhadada
Journal:  J Pediatr Endocrinol Metab       Date:  2009-10       Impact factor: 1.634

6.  Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic resonance imaging and anterior pituitary function.

Authors:  S Chen; J Léger; C Garel; M Hassan; P Czernichow
Journal:  J Clin Endocrinol Metab       Date:  1999-07       Impact factor: 5.958

7.  POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature.

Authors:  Swati Jadhav; Chakra Diwaker; Anurag R Lila; Jugal V Gada; Shantanu Kale; Vijaya Sarathi; Puja M Thadani; Sneha Arya; Virendra A Patil; Nalini S Shah; Tushar R Bandgar
Journal:  Pituitary       Date:  2021-03-20       Impact factor: 4.107

8.  Multi-genic pattern found in rare type of hypopituitarism: a whole-exome sequencing study of Han Chinese with pituitary stalk interruption syndrome.

Authors:  Qing-Hua Guo; Cheng-Zhi Wang; Zhi-Qiang Wu; Yan Qin; Bai-Yu Han; An-Ping Wang; Bao-An Wang; Jing-Tao Dou; Xiao-Sheng Wu; Yi-Ming Mu
Journal:  J Cell Mol Med       Date:  2017-07-14       Impact factor: 5.310

9.  Pituitary stalk transection syndrome: Comparison of clinico-radiological features in adults and children with review of literature.

Authors:  Chinmay Kulkarni; Srikanth Moorthy; Sreekumar K Pullara; R Rajeshkannan; Ambika G Unnikrishnan
Journal:  Indian J Radiol Imaging       Date:  2012-07

10.  Identification of novel candidate pathogenic genes in pituitary stalk interruption syndrome by whole-exome sequencing.

Authors:  Xuqian Fang; Yuwen Zhang; Jialin Cai; Tingwei Lu; Junjie Hu; Fei Yuan; Peizhan Chen
Journal:  J Cell Mol Med       Date:  2020-08-31       Impact factor: 5.310

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