Osteogenesis Imperfecta

Genetic_DisordersOriginal Editors - Barrett Mattingly from Bellarmine University's Pathophysiology of Complex Patient Problems project.

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Introduction

Osteogenesis imperfecta (OI) refers to a heterogeneous group of congenital, non-sex-linked, genetic disorders of collagen type I production, involving connective tissues and bones.

The hallmark feature of OI is osteoporosis and fragile bones that fracture easily, as well as, blue sclera, dental fragility and hearing loss. These features result in reduced mobility and function to complete everyday tasks.

OI affects not only the physical but also the social and emotional well-being of children, young people, and their families. The coordinated efforts of a multidisciplinary team can support children with OI to fulfill their potential, maximizing function, independence, and well-being.

Image 1: X ray for osteogenesis imperfecta

Types of OI

This image of Sean Stephenson is included courtesy of http://26.media.tumblr.com.

Three main types are easily distinguished

• Type I. Mildest and most common type. About 50% of all affected children have this type. There are few fractures and deformities
• Type II. Most severe type. A baby has very short arms and legs, a small chest, and soft skull. He or she may be born with fractured bones. He or she may also have a low birth weight and lungs that are not well developed. A baby with type II OI usually dies within weeks of birth
• Type III. Most severe type in babies who don’t die as newborns See image 2. At birth, a baby may have slightly shorter arms and legs than normal and arm, leg, and rib fractures. A baby may also have a larger than normal head, a triangle-shaped face, a deformed chest and spine, and breathing and swallowing problems. These symptoms are different in each baby.

Types IV to VIII are variable in severity and uncommon

Epidemiology

This picture of the Wyse family is included courtesy of the Agape Family Life House website agapeflh.org.

The estimated incidence is approximately 1 in every 12,000-15,000 births. OI occurs with equal frequency among males and females and across races and ethnic groups. The lifespan varies with the type.

Image 2: Twins with OI

Etiology

OI is a rare genetic disease. In the majority of cases, it occurs secondary to mutations in the COL1A1 and COL1A2 genes. More recently, there has been the identification of diverse mutations related to OI.

Pathology

A fundamental pathology in OI is a disturbance in the synthesis of type I collagen, which is the predominant protein of the extracellular matrix of most tissues. In bone, this defect results in osteoporosis, thus increasing the tendency to fracture. Besides bone, type I collagen is also a major constituent of dentine, sclerae, ligaments, blood vessels and skin.

Clinical presentation

The clinical presentation of osteogenesis imperfecta is highly variable, ranging from a mild form with no deformity, normal stature and few fractures to a form that is lethal during the perinatal period.

In general, four major clinical features characterise osteogenesis imperfecta:

1. Osteoporosis with abnormal bone fragility Image 4: X-ray OI eg Easily broken bones, Bone deformities, such as bowing of the legs, A barrel-shaped chest, A curved spine, A triangle-shaped face
2. Discoloration of the white of the eye (sclera), may be blue or gray in color
3. Dentinogenesis imperfecta, a disorder of tooth development. This condition causes the teeth to be discolored (most often a blue-gray or yellow-brown color) and translucent. Teeth are also weaker than normal, making them prone to rapid wear, breakage, and loss. These problems can affect both primary (baby) teeth and permanent teeth.
4. Hearing impairment

Other features include ligamentous laxity and hypermobility of joints, short stature and easy bruising.

Diagnosis

The baby's healthcare provider or the specialists may recommend the following diagnostic tests:

1. X-rays. These may show many changes such as weak or deformed bones and fractures.
2. Lab tests. Blood, saliva, and skin may be checked. The tests may include gene testing.
3. Dual Energy X-ray Absorptiometry scan (DXA or DEXA scan). To check for softening.
4. Bone biopsy. A sample of the hipbone is checked.

Treatment

The main goal of treatment is to prevent deformities and fractures. And, once your child gets older, to allow him or her to function as independently as possible.

Management options include:

• Surgical correction of deformities and the prevention of fractures
  • intramedullary rods with osteotomy are used to correct severe bowing of the long bones
  • intramedullary rods are also recommended for children who repeatedly fracture long bones
  • different types of rods (surgical nails) are available to address issues related to surgery, bone size, and the prospect for growth; the two major categories of rods are telescopic and non-telescopic.

• Care of fractures. The lightest possible materials are used to cast fractured bones. To prevent further problems, it is recommended that a child begin moving or using the affected area as soon as possible.
• Bisphosphonates
• Growth hormone therapy
• Dental procedures. Treatments, including capping teeth, braces, and surgery may be needed.
• Physical and occupational therapy. Both are very important in babies and children with OI.
• Assistive devices. Wheelchairs and other custom-made equipment may be needed as babies get older.

Prognosis

Varied across the diverse spectrum of the disease.

1. Age of onset of long bone fractures has been demonstrated as an important prognostic indicator for ambulatory ability.
2. Survival: The most significant indicators include the location of fractures, the severity of fractures and general radiographic appearance of the skeleton.
3. Engelbert et al. demonstrated that: children who achieved independent sitting or standing or both by 12 years of age, were finally able to ambulate; children who could achieve independent sitting or standing, or both, by the age of 12 months were likely to be able to walk

Complications

Complications may affect most body systems in a baby or child with OI. The risk of developing complications depends on the type and severity of your baby's OI. Complications may include the following:

• Respiratory infections, eg COVID 19, pneumonia
• Heart problems eg poor cardiac valve defects
• Kidney stones
• Joint problems
• Hearing loss
• Eye conditions and vision loss

Team Approach

Physical and occupational therapy are part of an interdisciplinary approach to treatment. The medical team may also include a primary care physician, orthopedist, geneticist, nutritionist, social worker, and psychologist. Children and adults with OI, especially those with spine curves which may affect pulmonary status, may regularly see a pulmonologist. Ideally planning ahead for rehabilitation is included in the preparation for surgery.

Physiotherapy

When working with individuals and families living with OI, therapists should keep these principles in mind: ƒ Listen. It is essential to listen to individuals with OI and their families and respect their input.

• Set Goals. Make goals incremental, realistic and achievable. ƒ
• Fear of Fractures is another serious constraint to movement. Establishing safe movement procedures, encouraging self-confidence and optimizing strength are strategies that can help resolve this issue. Passive range of motion is not recommended with new clients. ƒ
• Expect Success. With the proper environment and equipment, the majority of children and adults with OI can function well in many or most areas of daily life including but not limited to self-care, school and work.

Maximizing a person’s strength and function not only improves overall health and wellbeing, but also improves bone health, as mechanical stresses and muscle tension on bone help increase bone density. eg, deformities such as a flattened skull, a lordotic back, or tight hip flexor muscles can be prevented or minimized through therapy.

Approaches include:

1. Exercise and recreational activities including weight bearing activities (braces may be needed), and low-impact activities such as swimming, once precautions are defined.
2. Safe handling and encouraging different body positions and postures during the day to strengthen muscle groups and prevent deformities.
3. Adaptive equipment. The individual with OI may need a variety of mobility aides depending on the environment (cane, walker, manual or power wheelchair).
4. Environmental adaptations to the home, school or workplace.

Circumstances requiring intermittent or long-term physical and occupational therapy will include the following:

1. When a child with OI has delays or weakness in motor skills
2. When a child or adult with OI is recovering from a fracture, surgery or injury
3. When a person with OI experiences fear of movement and trying new skills and activities.
4. When a person with OI reaches a transition point in life, they must adapt to a new environment or require ADL training.

Children of Glass

Viewing OI: A documentary from the Discovery Channel titled "Children of Glass" courtesy of Youtube.com.

Diagno

• Yochum TR, Kulbaba S, Seibert RE. Osteogenesis Imperfecta in a Weightlifter. Journal of Manipulative and Physiological Therapeutics; 25: 334-339. 2002.
  
• Strevel EL, Adachi JD, Papaioannou A, McNamara M. Case Report: Osteogenesis Imperfecta Elusive Cause of Fractures. Canadian Family Physician; 51: 1655-1657.2005.
  
• Iwamoto J, Takeda T, Sato Y. Effect of Treatment With Alendronate in Osteogenesis Imperfecta Type I: A Case Report. The Keio Journal of Medicine; 53 (4): 251–255. 2004.
  
• Aoki T, Kuraoka S, Ohtani S, Kuroda Y. Aortic Valve Replacement in a Woman with Osteogenesis Imperfecta. Annals of Thoracic and Cardiovascular Surgery; 8(1): 51-53. 2002.

Resources

• http://www.oif.org
  
• http://www.genome.gov/25521839
• http://www.osteogenesisimperfecta.org
• http://www.nlm.nih.gov/medlineplus/osteogenesisimperfecta.html
• http://ghr.nlm.nih.gov/condition=osteogenesisimperfecta
  
• http://www.brittlebone.org
  

References