Olfaction evaluation and correlation with brain atrophy in Bardet-Biedl syndrome

• Published in: Clinical genetics Vol. 86; no. 6; pp. 521 - 529
• Main Authors: Braun, J.-J., Noblet, V., Durand, M., Scheidecker, S., Zinetti-Bertschy, A., Foucher, J., Marion, V., Muller, J., Riehm, S., Dollfus, H., Kremer, S.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-12-2014
• Subjects: Adolescent; Adult; Atrophy; Bardet-Biedl syndrome; Bardet-Biedl Syndrome - physiopathology; Brain; Brain - pathology; brain atrophy; Case-Control Studies; Female; Genetic disorders; Humans; Magnetic Resonance Imaging; Male; Medical research; Morphology; MRI; olfaction; Olfaction Disorders - etiology; Retinitis Pigmentosa - etiology; Smell - physiology; Young Adult; olfaction; Bardet-Biedl syndrome; MRI; brain atrophy
• ISSN: 0009-9163; 1399-0004
• DOI: 10.1111/cge.12391

Bardet‐Biedl syndrome (BBS) is a well‐recognized ciliopathy characterized by cardinal features namely: early onset retinitis pigmentosa, polydactyly, obesity, hypogonadism, renal and cognitive impairment. Recently, disorders of olfaction (anosmia, hyposmia) have been also described in BBS patients. Moreover, morphological brain anomalies have been reported and prompt for further investigations to determine whether they are primary or secondary to peripheral organ involvement (i.e. visual or olfactory neuronal tissue). The objective of this article is to evaluate olfactory disorders in BBS patients and to investigate putative correlation with morphological cerebral anomalies. To this end, 20 BBS patients were recruited and evaluated for olfaction using the University of Pennsylvania Smell Identification Test (UPSIT). All of them underwent a structural magnetic resonance imaging (MRI) scan. We first investigated brain morphological differences between BBS subjects and 14 healthy volunteers. Then, we showed objective olfaction disorders in BBS patients and highlight correlation between gray matter volume reduction and olfaction dysfunction in several brain areas.