Abstract

BackgroundNodding syndrome is an epidemic symptomatic generalized epilepsy syndrome of unknown cause in Eastern Africa. Some patients have extreme short stature. We hypothesized that growth failure in nodding syndrome is associated with specific endocrine dysfunctions. In this pilot study, we examined the relationship between serum hormone levels and stature, bone age and sexual development.ResultsWe recruited ten consecutive children, 13 years or older, with World Health Organization defined nodding syndrome and assessed physical growth, bone age, development of secondary sexual characteristics and serum hormone levels. Two children with incomplete results were excluded. Of the eight remaining, two had severe stunting (height for age Z [HAZ] score < -3) and three had moderate stunting (HAZ score between-3 and -2). The bone age was delayed by a median 3(range 0-4) years. Serum growth hormone levels were normal in all eight but the two patients with severe stunting and one with moderate stunting had low levels of Somatomedin C (Insulin like Growth Factor [IGF1]) and/or IGF binding protein 3 (IGFBP3), mediators of growth hormone function. A linear relationship was observed between serum IGF1 level and HAZ score. With the exception of one child, all were either pre-pubertal or in early puberty (Tanner stages 1 and 2) and in the seven, levels of the gonadotrophins (luteinising and follicle stimulating hormone) and the sex hormones (testosterone/oestrogen) were all within pre-pubertal ranges or ranges of early puberty. Thyroid function, prolactin, adrenal, and parathyroid hormone levels were all normal.ConclusionsPatients with nodding syndrome may have dysfunctions in the pituitary growth hormone and pituitary gonadal axes that manifest as stunted growth, delayed bone age and puberty. Studies are required to determine if such endocrine dysfunction is a primary manifestation of the disease or a secondary consequence of chronic ill health and malnutrition and if so, whether targeted interventions can improve outcome.

Highlights

  • Nodding syndrome is an epidemic symptomatic generalized epilepsy syndrome of unknown cause in Eastern Africa

  • We hypothesized that nodding syndrome is associated with specific endocrine dysfunctions and that such dysfunction may manifest with growth failure, delayed bone growth and puberty

  • This study explored if specific endocrine abnormalities in these patients was associated with the delayed growth and sexual development

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Summary

Introduction

Nodding syndrome is an epidemic symptomatic generalized epilepsy syndrome of unknown cause in Eastern Africa. There are an estimated 5000 - 10,000 affected children in the region [7] This probably symptomatic generalized epilepsy syndrome is characterized by head nodding determined to be atonic seizures [5], and complicated by the development of other seizure types, cognitive and motor decline, Several patients with nodding syndrome have extreme short stature and delayed development of secondary sexual characteristics [4]. The pathogenesis of this growth failure and delay in the onset of puberty are unknown. We assessed consecutive patients with nodding syndrome, measured serum hormone levels and examined the relationship between the hormone levels and stature, bone age and sexual development

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