Literature DB >> 24178788

High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.

Ruta Navardauskaite1, Petra Dusatkova, Barbora Obermannova, Roland W Pfaeffle, Werner F Blum, Dalia Adukauskiene, Natalija Smetanina, Ondrej Cinek, Rasa Verkauskiene, Jan Lebl.   

Abstract

CONTEXT: PROP1 gene mutations cause multiple pituitary hormone deficiency (MPHD).
OBJECTIVE: We sought to expand experience with PROP1 mutation carriers by studying a large cohort of Lithuanian patients. PATIENTS AND METHODS: Sixty-seven MPHD patients were tested for PROP1 defects. Perinatal and postnatal data were obtained from medical records. Hormonal investigations, pituitary imaging, and GH therapy were provided in a single center in Kaunas, Lithuania.
RESULTS: A biallelic PROP1 gene mutation was found in 47 subjects (70.1%), of which 46 were homozygous for 296delGA. Positive finding rate among MPHD and population prevalence of PROP1 defects in Lithuania (15.8 per million) were the highest reported to date. Patients' birth lengths/weights were normal. Testicular retention was noted in 31% of boys. Median height SD scores declined over years 1-5: -1.56, -2.34, -3.43, -3.52, and -3.70. Mid-parental height predicted severity of growth retardation at diagnosis (r2=0.30; P=.0001). Deficiencies of GH, TSH, ACTH, and FSH/LH were diagnosed in 44/44, 44/44, 19/44, and 22/44 subjects at median age of 5.5, 5.6, 13.1, and 15.0 years, respectively. Pituitary height ranged from 16.6 mm (+20.2 SD) to 1.4 mm (-15.5 SD) and declined with age (r2=0.27, P=.001). GH replacement (dose 0.027 mg/kg/d) led to height velocities 12.2; 9.1; 6.9; 6.8; 6.7; 5.6; and 5.7 cm/y (medians) at years 1-7 and final height SD scores (17 patients) -0.98±1.77 (-1.04±1.41 below target height; P=.008 vs 0).
CONCLUSIONS: High prevalence of PROP1 defects in Lithuania is due to 296delGA mutation, suggesting a founder effect.

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Year:  2013        PMID: 24178788     DOI: 10.1210/jc.2013-3090

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  11 in total

1.  Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency.

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Journal:  Endocrine       Date:  2019-05-15       Impact factor: 3.633

2.  Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.

Authors:  Firdevs Baş; Z Oya Uyguner; Feyza Darendeliler; Zehra Aycan; Ergun Çetinkaya; Merih Berberoğlu; Zeynep Şiklar; Gönül Öcal; Şükran Darcan; Damla Gökşen; Ali Kemal Topaloğlu; Bilgin Yüksel; Mehmet Nuri Özbek; Oya Ercan; Olcay Evliyaoğlu; Semra Çetinkaya; Yaşar Şen; Emre Atabek; Güven Toksoy; Banu Küçükemre Aydin; Rüveyde Bundak
Journal:  Endocrine       Date:  2014-12-11       Impact factor: 3.633

Review 3.  Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Authors:  Qing Fang; Akima S George; Michelle L Brinkmeier; Amanda H Mortensen; Peter Gergics; Leonard Y M Cheung; Alexandre Z Daly; Adnan Ajmal; María Ines Pérez Millán; A Bilge Ozel; Jacob O Kitzman; Ryan E Mills; Jun Z Li; Sally A Camper
Journal:  Endocr Rev       Date:  2016-11-09       Impact factor: 19.871

4.  Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations.

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6.  Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.

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Journal:  J Hum Genet       Date:  2017-03-30       Impact factor: 3.172

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8.  Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders.

Authors:  Sebastian Alexis Vishnopolska; Maria Florencia Mercogliano; Maria Andrea Camilletti; Amanda Helen Mortensen; Debora Braslavsky; Ana Keselman; Ignacio Bergadá; Federico Olivieri; Lucas Miranda; Roxana Marino; Pablo Ramírez; Natalia Pérez Garrido; Helen Patiño Mejia; Marta Ciaccio; Maria Isabel Di Palma; Alicia Belgorosky; Marcelo Adrian Martí; Jacob Otto Kitzman; Sally Ann Camper; Maria Ines Pérez-Millán
Journal:  J Clin Endocrinol Metab       Date:  2021-06-16       Impact factor: 6.134

9.  Novel Nucleotide Variations, Haplotypes Structure and Associations with Growth Related Traits of Goat AT Motif-Binding Factor (ATBF1) Gene.

Authors:  Xiaoyan Zhang; Xianfeng Wu; Wenchao Jia; Chuanying Pan; Xiangcheng Li; Chuzhao Lei; Hong Chen; Xianyong Lan
Journal:  Asian-Australas J Anim Sci       Date:  2015-10       Impact factor: 2.509

10.  Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Authors:  Fatma Derya Bulut; Semine Özdemir Dilek; Damla Kotan; Eda Mengen; Fatih Gürbüz; Bilgin Yüksel
Journal:  J Clin Res Pediatr Endocrinol       Date:  2020-01-17
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