期刊论文详细信息
Orphanet Journal of Rare Diseases
Selective cognitive and psychiatric manifestations in Wolfram Syndrome
Tamara Hershey3  Bess A. Marshall1  Tasha Doty2  Amal Al-lozi2  Anna Buttlaire2  Angela M. Reiersen2  Allison N. Bischoff2 
[1] Department of Cell Biology, Washington University School of Medicine, St. Louis, MO, USA;Department of Psychiatry, Washington University School of Medicine, 4525 Scott Avenue, St. Louis, 63110, MO, USA;Department of Radiology, Washington University School of Medicine, St. Louis, MO, USA
关键词: Diabetes mellitus;    Development;    Behavior;    Psychiatry;    Cognition;    Wolfram syndrome;   
Others  :  1211835
DOI  :  10.1186/s13023-015-0282-1
 received in 2015-02-19, accepted in 2015-05-11,  发布年份 2015
PDF
【 摘 要 】

Background

Wolfram Syndrome (WFS) is known to involve diabetes mellitus, diabetes insipidus, optic nerve atrophy, vision loss, hearing impairment, motor abnormalities, and neurodegeneration, but has been less clearly linked to cognitive, sleep, and psychiatric abnormalities. We sought to determine whether these abnormalities are present in children, adolescents, and young adults with WFS compared to age- and gender-matched individuals with and without type 1 diabetes using standardized measures.

Methods

Individuals with genetically-confirmed WFS (n = 19, ages 7–27) were compared to age- and gender- equivalent groups of individuals with type 1 diabetes (T1DM; n = 25), and non-diabetic healthy controls (HC: n = 25). Cognitive performance across multiple domains (verbal intelligence, spatial reasoning, memory, attention, smell identification) was assessed using standardized tests. Standardized self- and parent-report questionnaires on psychiatric symptoms and sleep disturbances were acquired from all groups and an unstructured psychiatric interview was performed within only the WFS group.

Results

The three groups were similar demographically (age, gender, ethnicity, parental IQ). WFS and T1DM had similar duration of diabetes but T1DM had higher HbA1C levels than WFS and as expected both groups had higher levels than HC. The WFS group was impaired on smell identification and reported sleep quality, but was not impaired in any other cognitive or self-reported psychiatric domain. In fact, the WFS group performed better than the other two groups on selected memory and attention tasks. However, based upon a clinical evaluation of only WFS patients, we found that psychiatric and behavioral problems were present and consisted primarily of anxiety and hypersomnolence.

Conclusions

This study found that cognitive performance and psychological health were relatively preserved WFS patients, while smell and sleep abnormalities manifested in many of the WFS patients. These findings contradict past case and retrospective reports indicating significant cognitive and psychiatric impairment in WFS. While many of these patients were diagnosed with anxiety and hypersomnolence, self-reported measures of psychiatric symptoms indicated that the symptoms were not of grave concern to the patients. It may be that cognitive and psychiatric issues become more prominent later in life and/or in later stages of the disease, but this requires standardized assessment and larger samples to determine. In the relatively early stages of WFS, smell and sleep-related symptoms may be useful biomarkers of disease and should be monitored longitudinally to determine if they are good markers of progression as well.

Trial Registration

Current Clinicaltrials.gov Trial NCT02455414 webcite.

【 授权许可】

   
2015 Bischoff et al.; licensee BioMed Central.

【 预 览 】
附件列表
Files Size Format View
20150611042144269.pdf 536KB PDF download
Fig. 2. 18KB Image download
Fig. 1. 10KB Image download
【 图 表 】

Fig. 1.

Fig. 2.

【 参考文献 】
  • [1]Wolfram DJ. Diabetes mellitus and simple optic atrophy among siblings: report of four cases. Mayo Clin Proc. 1938; 9:715-8.
  • [2]Takeda K, Inoue H, Tanizawa Y, Matsuzaki Y, Oba J, Watanabe Y et al.. WFS1 (Wolfram Syndrome 1) gene product : predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain. Hum Mol Genet. 2001; 10(5):477-84.
  • [3]Ishihara H, Takeda S, Tamura A, Takahashi R, Yamaguchi S, Takei D et al.. Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion. Hum Mol Genet. 2004; 13(11):1159-70.
  • [4]Yamada T, Ishihara H, Tamura A, Takahashi R, Yamaguchi S, Takei D et al.. WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic beta-cells. Hum Mol Genet. 2006; 15(10):1600-9.
  • [5]Akiyama M, Hatanaka M, Ohta Y, Ueda K, Yanai A, Uehara Y et al.. Increased insulin demand promotes while pioglitazone prevents pancreatic beta cell apoptosis in Wfs1 knockout mice. Diabetologia. 2009; 52(4):653-63.
  • [6]Yamamoto H, Hofmann S, Hamasaki D, Yamamoto H, Kreczmanski P, Schmitz C et al.. Wolfram Syndrome 1 (WFS1) protein expression in retinal ganglion cells and optic nerve glia of the cynomolgus monkey. Exp Eye Res. 2006; 83(5):1303-6.
  • [7]Lu S, Kanekura K, Hara T, Mahadevan J, Spears LD, Oslowski CM et al.. A calcium-dependent protease as a potential therapeutic target for Wolfram Syndrome. Proc Natl Acad Sci. 2014; 111(49):E5292-301.
  • [8]Hershey T, Lugar HM, Shimony JS, Rutlin J, Koller JM, Perantie DC et al.. Early brain vulnerability in Wolfram Syndrome. PLoS One. 2012; 7(7):e40604.
  • [9]Pickett KA, Duncan RP, Hoekel J, Marshall D, Hershey T, Earhart G et al.. Early presentation of gait impairment in Wolfram Syndrome. Orphanet J Rare Dis. 2012; 7(1):92. BioMed Central Full Text
  • [10]Marshall BA, Permutt MA, Paciorkowski AR, Hoekel J, Karzon R, Wasson J et al.. Phenotypic characteristics of early Wolfram Syndrome. Orphanet J Rare Dis. 2013; 8(1):64. BioMed Central Full Text
  • [11]Barrett TG, Bundey SE, Macleod AF. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) Syndrome. Lancet. 1995; 346:1458-63.
  • [12]Chaussenot A, Bannwarth S, Rouzier C, Vialettes B, Mkadem SA, Chabrol B et al.. Neurologic features and genotype-phenotype correlation in Wolfram Syndrome. Ann Neurol. 2011; 69(3):501-8.
  • [13]Nickl-Jockschat T, Kunert J, Heroertz-Dahlmann B, Grozinger M. Psychiatric symptoms in a patient with Wolfram Syndrome caused by a combination of thalamic deficit and endocrinological pathologies. Neurocase. 2008; 15(1):47-52.
  • [14]Hardy C, Khanim F, Torres R, Scott-Brown M, Seller A, Poulton J et al.. Clinical and molecular genetic analysis of 19 Wolfram Syndrome kindreds demonstrating a wide spectrum of mutations in WFS1. Am J Hum Genet. 1999; 65(5):1279-90.
  • [15]Waschbisch A, Volbers B, Struffert T, Hoyer J, Schwab S, Bardutzky J. Primary diagnosis of Wolfram Syndrome in an adult patient–case report and description of a novel pathogenic mutation. Neurol Sci. 2011; 300:191-3.
  • [16]Medlej R, Wasson J, Baz P, Azar S, Salti I, Loiselet J et al.. Diabetes mellitus and optic atrophy: a study of Wolfram Syndrome in the Lebanese population. J Clin Endocrinol Metab. 2004; 89(4):1656-61.
  • [17]Lessell S, Rosman NP. Juvenile diabetes mellitus and optic atrophy. Arch Neurol. 1977; 34(12):759-65.
  • [18]Verri A, Borutti G, Sandrini G, Poloni M, Vailati A. A case of Wolfram Syndrome: neurological features. Ital J Neurol Sci. 1982; 3:351-3.
  • [19]Nguyen C, Foster ER, Paciorkowski AR, Viehover A, Considine C, Bondurant A et al.. Reliability and validity of the Wolfram Unified Rating Scale (WURS). Orphanet J Rare Dis. 2012; 7(1):89. BioMed Central Full Text
  • [20]Wechsler D. Wechsler abbreviated scale of intelligence. 3rd ed. Psychological Corporation, Cleveland, OH; 1999.
  • [21]McGrew KS, Woodcock RW. Woodcock-Johnson III technical manual. Riverside Publishing, Itasca, IL; 2001.
  • [22]Wechsler D. Wechsler intelligence scale for children. 3rd ed. Psychological Corporation, Cleveland, OH; 1997.
  • [23]Wechsler D. Wechsler adult intelligence scale–III. Psychological Corporation, San Antonio, TX; 1997.
  • [24]Fridlund AJ, Delis DC. California verbal learning test–children’s version. Psychological Corporation, San Antonio, TX; 1994.
  • [25]Delis DC, Kaplan E. California verbal learning test-II. Psychological Corporation, San Antonio, TX; 2000.
  • [26]Conners CK, Epstein JN, Angold A, Klaric J. Continuous performance test performance in a normative epidemiological sample. J Abnorm Child Psychol. 2003; 31:555-62.
  • [27]Doty RL. The smell identification test administration manual. 3rd ed. Sensonics, Haddon Heights, NJ; 1995.
  • [28]Wechsler D. Wechsler test of adult reading: WTAR. Psychological Corporation, San Antonio, TX; 2001.
  • [29]Gadow KD, Sprafkin J. Child symptom inventory-4 screening and norms manual. Checkmate Plus, Stony Brook, NY; 2002.
  • [30]Gadow KD, Sprafkin J, Weiss MD. Adult self-report-4 manual. Checkmate Plus, Stony Brook, NY; 2004.
  • [31]Gadow KD, Sprafkin J. Youth’s inventory-4 manual. Checkmate Plus, Stony Brook, NY; 1999.
  • [32]Chervin RD, Hedger K, Dillon JE, Pituch KJ. Pediatric sleep questionnaire (PSQ): validity and reliability of scales for sleep-disordered breathing, snoring, sleepiness, and behavioral problems. Sleep Med. 2000; 1:21-32.
  • [33]Buysse DJ, Reynolds CF, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh sleep quality index: a new instrument psychiatric practice and research. Psychiatry Res. 1989; 28:193-213.
  • [34]Harris PA, Taylor Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)–a metadata-driven methodology and workflow process for providing translational research informatict support. J Biomed Inform. 2009; 42(2):377-81.
  • [35]Sequeira A, Kim C, Seguin M, Lesage A, Chawsky N, Desautels A et al.. Wolfram syndrome and suicide: evidence for a role of WFS1 in suicidal and impulsive behavior. Am J Med Genet B Neuropsychiatr Genet. 2003; 119B(1):108-13.
  • [36]Swift M, Swift RG. Wolframin mutations and hospitalization for psychiatric illness. Mol Psychiatry. 2005; 10(8):799-803.
  • [37]Okten A, Gedik Y, Demirci A, Mocan H, Erduran E, Aslan Y. Various clinical aspects of DIDMOAD (Wolfram) Syndrome. Turk J Pediatr. 1995; 37:235-40.
  • [38]Genís D, Davalos A, Molins A, Ferrer I. Wolfram Syndrome: a neuropathological study. Acta Neuropathol. 1997; 93(4):426-9.
  • [39]Jackson MJ, Bindoff LA, Weber K, Wilson JN, Ince P, Alberti KG et al.. Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Diabetes Care. 1994; 17(7):728-33.
  • [40]Strous RD, Shoenfeld Y. To smell the immune system: olfaction, autoimmunity and brain involvement. Autoimmun Rev. 2006; 6(1):54-60.
  • [41]Matyka KA, Crawford C, Wiggs L, Dunger DB, Stores G. Alterations in sleep physiology in young children with insulin-dependent diabetes mellitus: relationship to nocturnal hypoglycemia. J Pediatr. 2000; 137(2):233-8.
  • [42]Estrada CL, Danielson KK, Drum ML, Lipton RB. Insufficient sleep in young patients with diabetes and their families. Biol Res Nurs. 2012; 14(1):48-54.
  • [43]Perfect MM, Patel PG, Scott RE, Wheeler MD, Patel C, Griffin K et al.. Sleep, glucose, and daytime functioning in youth with type 1 diabetes. Sleep. 2012; 35(1):81-8.
  • [44]Caruso NC, Radovanovic B, Kennedy D, Couper J, Kohler M, Kavanagh PS et al.. Sleep, executive functioning and behaviour in children and adolescents with type 1 diabetes. Sleep Med. 2014; 15(12):1490-9.
  • [45]Colavito V, Tesoriero C, Wirtu AT, Grassi-Zucconi G, Bentivoglio M. Limbic thalamus and state-dependent behavior: the paraventricular nucleus of the thalamic midline as a node in circadian timing and sleep/wake-regulatory networks. Neurosci Biobehav Rev. 2014. http://www.sciencedirect.com/science/article/pii/S014976341400325X.
  文献评价指标  
  下载次数:27次 浏览次数:13次