International Journal of Molecular Sciences (Feb 2024)

High-Titer Anti-ZSCAN1 Antibodies in a Toddler Clinically Diagnosed with Apparent Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation Syndrome

  • Vlad Tocan,
  • Akari Nakamura-Utsunomiya,
  • Yuri Sonoda,
  • Wakato Matsuoka,
  • Soichi Mizuguchi,
  • Yuichiro Muto,
  • Takaaki Hijioka,
  • Masao Nogami,
  • Daiki Sasaoka,
  • Fusa Nagamatsu,
  • Utako Oba,
  • Naonori Kawakubo,
  • Hiroshi Hamada,
  • Yuichi Mushimoto,
  • Pin Fee Chong,
  • Noriyuki Kaku,
  • Yuhki Koga,
  • Yasunari Sakai,
  • Yoshinao Oda,
  • Tatsuro Tajiri,
  • Shouichi Ohga

DOI
https://doi.org/10.3390/ijms25052820
Journal volume & issue
Vol. 25, no. 5
p. 2820

Abstract

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Severe obesity in young children prompts for a differential diagnosis that includes syndromic conditions. Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD) syndrome is a potentially fatal disorder characterized by rapid-onset obesity associated with hypoventilation, neural crest tumors, and endocrine and behavioral abnormalities. The etiology of ROHHAD syndrome remains to be established, but recent research has been focusing on autoimmunity. We report on a 2-year-old girl with rapid-onset obesity during the first year of life who progressed to hypoventilation and encephalitis in less than four months since the start of accelerated weight gain. The patient had a high titer of anti-ZSCAN1 antibodies (348; reference range < 40), and the increased values did not decline after acute phase treatment. Other encephalitis-related antibodies, such as the anti-NDMA antibody, were not detected. The rapid progression from obesity onset to central hypoventilation with encephalitis warns about the severe consequences of early-onset ROHHAD syndrome. These data indicate that serial measurements of anti-ZSCAN1 antibodies might be useful for the diagnosis and estimation of disease severity. Further research is needed to determine whether it can predict the clinical course of ROHHAD syndrome and whether there is any difference in antibody production between patients with and without tumors.

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