Genetic Regulators of Bone Health That Are Unique to Vertebral Bone

Официальное название

Identification and Characterization of Genetic Regulators of Bone Health That Are Unique to Vertebral Bone.

Обзор

Osteoporosis is an age related disease in which a person's bone slowly becomes weaker with time. The bones may become so weak that they break easily such as a fall from standing height. The most commonly broke bones in osteoporosis are those of the hip, the spine or the wrist. Osteoporosis runs in families meaning that genetic differences explain why some people break bones in old age and other do not. Genetic studies have been done that show the the genes associated with spine (vertebral) fractures (broken bones) and hip fractures are different, suggesting that osteoporosis of the spine is not the exact same disease as osteoporosis of the hip. Genetic studies tell us what part of the genome (i.e. genes) are associated with a disease, but do not tell us how these genes act biologically to cause that disease. In this study, we seek to determine how the genes uniquely associated with spine osteoporosis behave in normal and aged bone, to determine how they interact with each other as a team to impact spine bone. In this study, we will measure gene activity (so called gene expression) in bone samples taken from people undergoing major spine deformity surgery. We will using genetic data from these patients to determine how gene activity is controlled in bone and how that relates to measures of bone health such as bone mineral density data. The results of this study will provide critical data regarding how osteoporosis of the spine happens, and these data will be used to find better and safer treatments to prevent bone fractures of the spine that happen with age.

Вмешательства

• Другое Sample collection for gene expression
  This is a cross-sectional sample collection study. Vertebral bone tissue that would otherwise be discarded is collected from patients undergoing surgery to correct a spine deformity and gene expression is measure in these tissues.

Первичные конечные точки

• Gene and transcript quantification [Срок оценки: Baseline]
• Genotypes [Срок оценки: Baseline]

Вторичные конечные точки (4)

• Expression quantitative trait loci (eQTL) [Срок оценки: Baseline]
• Co-localization [Срок оценки: Baseline]
• Expression-phenotype correlation [Срок оценки: Baseline]
• Co-expression Network [Срок оценки: Baseline]

Критерии участия

Критерии включения

• Men and women between the ages of 18 and 85 undergoing a multi-level spinal fusion (i.e. a T10 (or higher) fusion to the pelvis) -OR- a 3 column osteotomy with a corpectomy from for short segment surgeries -OR- a vertebral column resection (VCR) involving a corpectomy -OR- any deformity correction surgery wherein the attending surgeon determines that a large amount of bone containing trabecular elements will be removed and discarded.
• Willing and able to provide informed consent

Критерии исключения

• End stage renal disease.
• Any history of cancer.
• Reliance on a wheelchair for 70% or greater of their mobility for longer than 12 months.
• Quadra or paraplegia due to spinal cord injury.
• Current use of epilepsy medications.
• Confirmed Marfans, osteogenesis imperfecta or other genetic syndrome known to impact bone formation (Guacher's, Vit D independent rickets, etc).
• Current glucocorticoid use lasting longer than 3 months, or greater than 6 months lifetime use.
• Current or suspected current infection associated with orthopedic hardware.
• HIV or Hep C positive and or currently on anti-viral medications.
• History of gastric bypass surgery and or weigh loss exceeding 100 pounds.
• Primary or secondary hyperparathyroidism.
• Paget's disease

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения

Когортное

Центры проведения

США · 1 центр

• Univeristy of Colorado Denver — Aurora

Идентификаторы

NCT: NCT05946278 · 23-0602

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

Открыть это исследование на ClinicalTrials.gov ↗