Test 3 SCD & CF Flashcards
causation of SCD
Caused by a mis-sense mutation in the 6th codon of the beta chain of Hemoglobin
What is the most common form of SCD?
Hb SS
SCD: mutation
- glutamate converted into valine on the 6th codon
- Glu is hydrophilic
- Val is hydrophobic
- causes insoluble rod-like clumps
SCD: what does the hydrophobic surface cause?
polymerization of deoxyhemoglobin
consequences of SCD
- Pain crises
- Chronic pain
- Severe anemia
- Infections
- Spleen sequestration
- Gall stones
- Priapism
- Brain stroke
- Silent Brain injury
- Organ failure (including eyes & blindness)
- Acute Chest syndrome
initial symptoms of SCD
- Dactylitis: swelling of hands & feet
- Fatigue, fussiness
- Yellowish skin (jaundice)
- Yellowish eyes (icteris)
- Shortness of breath
diagnostic tests: SCD
- prenatal: test amniotic fluid or tissue from placenta
- newborn test: 5-40 day old
- filter paper test: clot = positive for SCD
- Gel Electrophoresis - HbA will run deeper in the gel b/c it’s more negative
- PCR & restriction enzyme digestion: look @ notes for visual sl19
SCD therapy
- treat symptoms: pain, anemia, infections
- hydroxyurea increases fetal Hb (protects against HbS side effects)
- cure: myeloablative Hematopoietic Stem Cell Transplantation
- CRISPR/Cas 9: edit stem cell to have HbA gene and engraft in bone marrow
- Voxelotor: increases Hb’s affinity to O2
CF: mutation
various mutations in the CFTR gene -> encodes a chloride ion channel that regulates salt and water movement in cells -> thick, sticky mucus and salty sweat
most common CF mutation in US
3-base pair deletion ∆F508 or Phe508del -> loss of Phenylalanine at position 508 of the protein
initial symptoms of CF
- salty skin
- baby doesn’t pass stool
- frequent coughing
- thick sputum / bloody
- abd discomfort / pain
- large, greasy stools
- poor weight gain and growth
consequences of CF
- blocked airways -> trouble breathing
- mucus in airways -> infections
- Pneumothorax & bronchiectasis
- Blocked pancreas -> no digestive enzymes -> constipation, dehydration
- Salty sweat -> dehydration, increased heart rate, heat stroke, ↓ BP
- ↑ risk for diabetes
- osteoporosis, osteopenia, clubbing
- infertility
- respiratory failure
diagnostic tests: CF
- newborn heel prick: genetic test and pancreatic function test
- sweat test: topical pilocarpine applied to skin, electrical current induces sweating, sweat collected, measure for Cl content, 30, 30-59, 60 mEq/L
CF therapy
- antibiotics
- nebulizers
- bronchodilators
- chest physical therapy
- pancreatic enzyme
- vitamins
- increased fluid consumption
- Ivacaftor (Kalydeco®)
- Lumacaftor/Ivacaftor (Orkambi ®)
Ivacaftor (Kalydeco®)
- CFTR conductance potentiator
- For patients > 6 yrs of age with select mutation G551D
- Improves lung function & increases weight
- Reduces exacerbations by 25-50%
- Oral administration – every 12 hrs