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. 2022 Nov;45(11):2165-2170.
doi: 10.1007/s40618-022-01860-0. Epub 2022 Jul 19.

MKRN3 circulating levels in Prader-Willi syndrome: a pilot study

M Mariani  1 , D Fintini  2 , G Cirillo  3 , S Palumbo  3 , E M Del Giudice  3 , S Bocchini  2 , M Manco  4 , M Cappa  2 , A Grandone  3
Affiliations

MKRN3 circulating levels in Prader-Willi syndrome: a pilot study

M Mariani et al. J Endocrinol Invest. 2022 Nov.

Abstract

Context: Hypogonadism in Prader-Willi syndrome (PWS) is generally attributed to hypothalamic dysfunction or to primary gonadal defect. MKRN3, a maternal imprinted gene located on 15q11.2-q13 region, encodes makorin ring finger protein 3, whose deficiency causes precocious puberty, an extremely rare symptom in PWS.

Objective: This study aimed to evaluate MKRN3 levels in patients with PWS and to analyze its correlation with sexual hormone levels, insulin resistance and Body Mass Index (BMI).

Methods: We performed an observational cross-sectional study and enrolled 80 patients with genetically confirmed diagnosis of PWS with median age of 9.6 years.

Results: MKRN3 levels were measurable in 49 PWS patients with a geometric mean of 34.9 ± 22 pg/ml (median: 28.4). Unmeasurable levels of MKRN3 were found in 31 patients. No statistically significant differences were found between patients with and without measurable MKRN3 levels for any clinical, biochemical, or genetic characteristics. However, MKRN3 levels were inversely correlated with HOMA-IR index (p: 0.005) and HbA1c (p: 0.046) values. No statistically significant correlations were found between MKRN3 and LH, estradiol and testosterone concentrations, pubertal development and genetic defect, whereas a direct correlation with FSH was found (p: 0.007).

Conclusions: The typical genetic defect of PWS should lead to unmeasurable levels of the MKRN3 protein due to the inactivation of the paternal allele. Measurable circulating MKRN3 could suggest the possible involvement of tissue-specific imprinting mechanisms and other regulatory factors in gene expression. Correlations with HOMA-IR index, HbA1c, and FSH suggest peripheral actions of MKRN3, but future studies are warranted to investigate this topic.

Keywords: Hypogonadism; MKRN3; Prader Willi; Puberty.

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