Literature DB >> 24788131

Brain changes in Kallmann syndrome.

R Manara1, A Salvalaggio2, A Favaro3, V Palumbo4, V Citton5, A Elefante6, A Brunetti6, F Di Salle7, G Bonanni8, A A Sinisi4.   

Abstract

BACKGROUND AND
PURPOSE: Kallmann syndrome is a rare inherited disorder due to defective intrauterine migration of olfactory axons and gonadotropin-releasing hormone neurons, leading to rhinencephalon hypoplasia and hypogonadotropic hypogonadism. Concomitant brain developmental abnormalities have been described. Our aim was to investigate Kallmann syndrome-related brain changes with conventional and novel quantitative MR imaging analyses.
MATERIALS AND METHODS: Forty-five male patients with Kallmann syndrome (mean age, 30.7 years; range, 9-55 years) and 23 age-matched male controls underwent brain MR imaging. The MR imaging study protocol included 3D-T1, FLAIR, and diffusion tensor imaging (32 noncollinear gradient-encoding directions; b-value=800 s/mm2). Voxel-based morphometry, sulcation, curvature, and cortical thickness analyses and tract-based spatial statistics were performed by using Statistical Parametric Mapping 8, FreeSurfer, and the fMRI of the Brain Software Library.
RESULTS: Corpus callosum partial agenesis, multiple sclerosis-like white matter abnormalities, and acoustic schwannoma were found in 1 patient each. The total amount of gray and white matter volume and tract-based spatial statistics measures (fractional anisotropy and mean, radial, and axial diffusivity) did not differ between patients with Kallmann syndrome and controls. By specific analyses, patients with Kallmann syndrome presented with symmetric clusters of gray matter volume increase and decrease and white matter volume decrease close to the olfactory sulci; reduced sulcal depth of the olfactory sulci and deeper medial orbital-frontal sulci; lesser curvature of the olfactory sulcus and sharper curvature close to the medial orbital-frontal sulcus; and increased cortical thickness within the olfactory sulcus.
CONCLUSIONS: This large MR imaging study on male patients with Kallmann syndrome featured significant morphologic and structural brain changes, likely driven by olfactory bulb hypo-/aplasia, selectively involving the basal forebrain cortex.
© 2014 by American Journal of Neuroradiology.

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Year:  2014        PMID: 24788131      PMCID: PMC7966280          DOI: 10.3174/ajnr.A3946

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  37 in total

Review 1.  Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations.

Authors:  S B Seminara; F J Hayes; W F Crowley
Journal:  Endocr Rev       Date:  1998-10       Impact factor: 19.871

2.  Kallmann's syndrome and schizophrenia.

Authors:  George A Vagenakis; Thomas N Hyphantis; Charalabos Papageorgiou; Anthi Protonatariou; Argyro Sgourou; Panayotis A Dimopoulos; Venetsanos Mavreas; Apostolos G Vagenakis; Neoklis A Georgopoulos
Journal:  Int J Psychiatry Med       Date:  2004       Impact factor: 1.210

3.  Gender difference analysis of cortical thickness in healthy young adults with surface-based methods.

Authors:  Kiho Im; Jong-Min Lee; Junki Lee; Yong-Wook Shin; In Young Kim; Jun Soo Kwon; Sun I Kim
Journal:  Neuroimage       Date:  2006-01-19       Impact factor: 6.556

4.  Kallmann's syndrome: mirror movements associated with bilateral corticospinal tract hypertrophy.

Authors:  M Krams; R Quinton; J Ashburner; K J Friston; R S Frackowiak; P M Bouloux; R E Passingham
Journal:  Neurology       Date:  1999-03-10       Impact factor: 9.910

5.  Diagnosis of X-recessive Kallmann syndrome in early infancy. Evidence of hypoplastic rhinencephalon.

Authors:  R Birnbacher; K Wandl-Vergesslich; H Frisch
Journal:  Eur J Pediatr       Date:  1994-04       Impact factor: 3.183

6.  Kallmann syndrome.

Authors:  Catherine Dodé; Jean-Pierre Hardelin
Journal:  Eur J Hum Genet       Date:  2008-11-05       Impact factor: 4.246

7.  Kallmann syndrome: MR evaluation of olfactory system.

Authors:  D M Yousem; W J Turner; C Li; P J Snyder; R L Doty
Journal:  AJNR Am J Neuroradiol       Date:  1993 Jul-Aug       Impact factor: 3.825

8.  Histopathology of olfactory mucosa in Kallmann's syndrome.

Authors:  J E Schwob; K E Szumowski; D A Leopold; P Emko
Journal:  Ann Otol Rhinol Laryngol       Date:  1993-02       Impact factor: 1.547

9.  Kallman syndrome versus idiopathic hypogonadotropic hypogonadism at MR imaging.

Authors:  T J Vogl; J Stemmler; B Heye; J Schopohl; A Danek; C Bergman; J O Balzer; R Felix
Journal:  Radiology       Date:  1994-04       Impact factor: 11.105

10.  Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome.

Authors:  M Schwanzel-Fukuda; D Bick; D W Pfaff
Journal:  Brain Res Mol Brain Res       Date:  1989-12
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Review 2.  Neuroanatomical and molecular correlates of cognitive and behavioural outcomes in hypogonadal males.

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4.  Rhinencephalon changes in tuberous sclerosis complex.

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Review 5.  Arachnoid cyst: a further anomaly associated with Kallmann syndrome?

Authors:  Luca Massimi; Alessandro Izzo; Giovanna Paternoster; Paolo Frassanito; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2016-07-05       Impact factor: 1.475

6.  Spectral signatures of mirror movements in the sensori-motor connectivity in kallmann syndrome.

Authors:  Renzo Manara; Federica Di Nardo; Alessandro Salvalaggio; Antonio Agostino Sinisi; Guglielmo Bonanni; Vincenzo Palumbo; Elena Cantone; Arturo Brunetti; Francesco Di Salle; Arianna D'errico; Andrea Elefante; Fabrizio Esposito
Journal:  Hum Brain Mapp       Date:  2017-09-30       Impact factor: 5.038

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Authors:  Joshua S Shimony; Christopher D Smyser; Graham Wideman; Dimitrios Alexopoulos; Jason Hill; John Harwell; Donna Dierker; David C Van Essen; Terrie E Inder; Jeffrey J Neil
Journal:  Neuroimage       Date:  2015-11-06       Impact factor: 6.556

8.  Dynamic spectral signatures of mirror movements in the sensorimotor functional connectivity network of patients with Kallmann syndrome.

Authors:  Federica Di Nardo; Renzo Manara; Antonietta Canna; Francesca Trojsi; Gianluca Velletrani; Antonio Agostino Sinisi; Mario Cirillo; Gioacchino Tedeschi; Fabrizio Esposito
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9.  A novel PNPLA6 compound heterozygous mutation identified in a Chinese patient with Boucher‑Neuhäuser syndrome.

Authors:  Ruizhi Zheng; Yaguang Zhao; Jiayu Wu; Yuanmei Wang; Jian-Ling Liu; Zhi-Ling Zhou; Xiao-Tao Zhou; Dan-Na Chen; Wei-Hua Liao; Jia-Da Li
Journal:  Mol Med Rep       Date:  2018-05-03       Impact factor: 2.952

Review 10.  Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption.

Authors:  Yujun Liu; Xu Zhi
Journal:  Reprod Sci       Date:  2021-07-06       Impact factor: 2.924

  10 in total

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