stickler syndrome study at the national institutes of health nazli mcdonnell m d ph d l.
Download
Skip this Video
Loading SlideShow in 5 Seconds..
Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D. PowerPoint Presentation
Download Presentation
Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D.

Loading in 2 Seconds...

play fullscreen
1 / 25

Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D. - PowerPoint PPT Presentation


  • 272 Views
  • Uploaded on

Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D. Laboratory of Clinical Investigation National Institute on Aging National Institutes of Health Baltimore, Maryland. Introduction.

loader
I am the owner, or an agent authorized to act on behalf of the owner, of the copyrighted work described.
capcha
Download Presentation

Stickler Syndrome Study at the National Institutes of Health Nazli McDonnell M.D., Ph.D.


An Image/Link below is provided (as is) to download presentation

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.


- - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - -
Presentation Transcript
stickler syndrome study at the national institutes of health nazli mcdonnell m d ph d

Stickler Syndrome Study at the National Institutes of HealthNazli McDonnell M.D., Ph.D.

Laboratory of Clinical Investigation

National Institute on Aging

National Institutes of Health

Baltimore, Maryland

introduction
Introduction
  • Stickler Syndrome is an autosomal dominant hereditary disorder that effects the connective tissue
  • 1 in 10,000 individuals in North America (Hermann et al, 1975) are thought to have Stickler Syndrome
  • Stickler Syndrome may affect your eyes, your hearing, your bones and joints
intro cont
Intro cont.
  • Known mutations that lead to Sticklers are found on the Col2A1, Col11A1 and the Col11A2 genes
  • They are genes code for the collagens that are found in your eyes, joints and bones
  • Mutations on these genes account for around 50% of the cases of Stickler Syndrome. Other causes for Sticklers syndrome are unknown at this time.
manifestations
Manifestations
  • Stickler Syndrome effects many parts of the body.
  • In the eyes, Stickler syndrome may cause near-sightedness (myopia), vitreous degeneration, retinal detachments and retinal tearing, premature cataracts and glaucoma
  • People with Stickler Syndrome may be born with cleft palates and/or bifid uvulas
manifestations cont
Manifestations cont.
  • The most noticeable manifestations of Stickler are the facial manifestations. People with Sticklers Syndrome often have a flattened facial profile, flattened and broadened nasal bridge and small chins.
  • Patients also have problems with high frequency hearing loss and hypermobile tympanic membranes
diagnosis is often missed
Diagnosis is often missed
  • Stickler syndrome is among the most common autosomal dominant connective tissue disorders but is often unrecognized and therefore not diagnosed by clinicians.
  • Ten percent of patients with isolated cleft palate and 12% with the Pierre-Robin sequence were found to have undiagnosed Stickler syndrome in one series [Kronwith et al., 1990; Sheffield et al., 1987] The actual incidence is higher.
background
Background
  • Collagens are the most common proteins in the extracellular matrix
  • Collagen Type II is abundant in the vitreous of the eye, the spinal column, cartridge, and inner ear
  • Type II is also present in many tissues during embryological development
  • Collagen XI is found in association with Collagen II.
the collagens
The Collagens
  • Collagens consists of three polypeptide chains which are folded into a rod-like triple helical molecule
  • Each of the constituent chains of the triple helix are called alpha chains and are coiled in a left handed helix with three amino acids per turn.
  • The constituent amino acids are regularly arranged in the order Gly-X-Y such that glycine, which is the smallest of all amino acids, occupies the restricted space in which the three  helical chains come together.
  • This arrangement is crucial for the stability of the macromolecule.
collagen structure
Collagen structure

Side view shows:

Primary structure = (X-Y-gly)n

X,Y are often lysine or proline

Top end view shows:

Secondary structure is a

collagen helix with pitch

of 3.0 residues per turn

collagens and stickler syndrome
Collagens and Stickler Syndrome
  • Type 2 collagen is a homotrimer of three COL2A1 gene products, whereas type 11 collagen is a heterotrimer containing one each of the COL2A1, COL11A1, and COL11A2 gene products.
  • Both type 2 and 11 collagens are members of the fibrillar collagens, which are primarily found in cartilage, vitreous, and nucleus pulposus (soft, gelatinous central portion of an intervertebral disk).
the diagnostic criteria
The diagnostic criteria
  • Orofacial Abnormalities (2 points maximum)
  • (2 points) Cleft palate (open cleft, submucous cleft, or bifid uvula) (Major)
  • (1 point) Characteristic facies (malar hypoplasia, broad nasal bridge,
  • Micro/retrognathia)
  • Ocular Abnormalities (2 points maximum)
  • (2 points) Characteristic vitreous changes or retinal abnormalities (lattice degeneration, retinal holes, or retinal tear, retinal detachment) (Major)
  • Auditory Abnormalities (2 points maximum)
  • (2 points) High frequency sensorineural hearing loss (Major)
  • Age < 20: threshold  20 dB at 4-8 kHz
  • Age 20-40: threshold  30 dB at 4-8 kHz
  • Age > 40: threshold  40 dB at 4-8 kHz
  • (1 point) Hypermobile tympanic membranes
  • Skeletal Abnormalities (2 points maximum)
  • (1 point) History of femoral head failure
  • (slipped epiphysis or Legg-Perthes like disease)
  • (1 point) Radiographically demonstrated osteoarthritis before age 40
  • (1 point) scoliosis, spondylolisthesis, or Scheuermann-like kyphotic deformity
  • Family History / Molecular Data
  • (1 point) Independently affected 1st degree relative in a pattern consistent with autosomal dominant inheritance or presence of COL2A1, COL11A1, or
  • COL11A2 mutation associated with Stickler syndrome
  • Diagnosis requires: 5 or more points total up to 9 points
  • At least one 2-point major manifestation
  • Absence of features suggestive of a skeletal dysplasia (e.g. stature <5% centile)
genotype phenotype correlations
Genotype/Phenotype Correlations
  • Study involved 48 families suspected of having Stickler Syndrome
  • Consent was received from each individual to allow the NIA to collect data and genetic material from each patient
  • Patients underwent a detailed clinical genetics examination, dilated ophthalmology exam, audiology and otolaryngology evaluations
materials and methods contd
Materials and methods contd.
  • In most cases, radiographs of the spine and hip were available
  • The enrollment and tests took place before the development of the diagnostic criteria for Stickler syndrome.
  • Forty eight probands were selected from each family for molecular genetic analysis
  • Col2A1 and Col11A1 genes were amplified by polymerase chain reaction (PCR) and were screened for mutations
results
Results
  • 23 mutations in Col2A1 and 4 mutations in Col11A1 was found in our cohort of 48 probands.
  • All persons included in the study had orofacial features, while clefting of palate/uvula showed intra and inter family variability
  • All persons also had ocular involvement in the form of vitreous or retinal changes.
types of mutations
Types of Mutations
  • STOP = 16
  • Splice Site = 8
  • Insertion = 1
  • Arg/Cys = 1
  • Other missense =1
results contd
Results contd.
  • Hearing loss, premature osteoarthritis, and skeletal involvement was common.
  • Femoral head failure occurred in 3 families.
  • Hip or knee pain needs to be taken very seriously in children with Stickler syndrome as it can be a manifestation of femoral head failure.
summary of findings
Summary of Findings
  • Facial features 29/29
  • Open Cleft 11/29
  • Submucus Cleft 7/29
  • Bifid Uvula 5/29
  • Vitreous Change 24/29
  • Retinal Change 24/29
  • Vitreous OR Retinal Change 29/29
  • High frequency sensory neural hearing loss 17/29
  • Hypermobile Tympanic Membranes 2/29
  • Femoral Head Failure 3/29
  • Premature Osteoarthritis 16/29
  • Skeletal Abnormalities 14/29
discussion
Discussion
  • The mutation detection rate in this Stickler Syndrome cohort was 56%
  • All subjects with a mutation in Col2A1 or Col11A1 met the recently published Stickler Diagnostic Criteria
  • The majority of the mutations detected resulted in a splice site aberration (often implicated in exon skipping) or a premature termination codon.
discussion contd
Discussion Contd.
  • The phenotype analysis revealed that ocular involvement and craniofacial dysmorphisms are core features of Stickler syndrome.
  • Comparison with a large pedigree without a Col2A1/Col11A1 mutation in the proband reveals that this family has a phenotype indistinguishable from the subjects with such mutations
mutations in stickler syndrome
Mutations in Stickler Syndrome
  • All of the mutations found resulted in haploinsufficiency (inadequate amount of collagen, as opposed to abnormal collagen)
  • Dominant negative mutations in Collagen II result in the dwarfisms
  • This opens the door to the possibility that symptoms of Stickler syndrome may be treated by a mechanism that increases collagen production from the “good copy” of the gene.
future directions
Future directions
  • The next project will be to study the genes of the individuals who lack known mutations.
  • We are studying a candidate gene, CSPG2, which has been implicated in a family with Wagner syndrome which is a disease that affects the eye very similarly to Stickler syndrome.
future directions23
Future Directions
  • Tissues from patients with the known mutations will be analyzed to learn more about how the mutations effect the workings of the collagen
  • Phenotype analysis will continue to better understand the syndrome
enrollment of new patients
Enrollment of new patients
  • We will start to enroll new patients soon
  • Eye exam is now available for the study in its new location in Baltimore, however we are working on the details of transportation of participants
  • Hope to enroll 20 patients in 2008
acknowledgements
Acknowledgements

Ben Griswold, Minna Männikko, Jeremy Wells, Marja Majava-Elo, Joseph Tran, Katherine Mandel , Peter S. Rose, Howard P. Levy,Joie Davis, Yvonne Szymko, Benjamin Rubin, Ekaterini Tsilou, Muriel Kaiser, Andrew J. Griffith, Ruth Altshuler Liberfarb, Leena Ala-Kokko, Clair A. Francomano

1 Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health

2 Department of Medical Biochemistry and Molecular Biology, University of Oulu

3 Department of Genetics, Massachusetts General Hospital

4 Clinical Research Branch, National Institute on Aging, National Institutes of Health

5 Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota

6 Department of Internal Medicine, Johns Hopkins University School of Medicine

7 National Human Genome Research Institute, National Institutes of Health

8 National Eye Institute, National Institutes of Health

9 National Institute on Deafness and Other Communication Disorders, National Institutes of Health

10Laboratory of Genetics, National Institute on Aging, National Institutes of Health

11Ursinus College, Collegeville, Pennsylvania