Total Protein in Serum

Total protein in serum (serum protein; serum protein) is composed of:

  • Albumin
  • Alpha-1 globulins
  • Alpha-2 globulins
  • Beta globulins
  • Gamma globulins

Albumin represents the main group here with circa 60%. The various fractions have multiple functions, such as transport, immune defense or blood clotting, among others.

The process

Material required

  • Blood serum

Preparation of the patient

  • Not necessary

Disruptive factors

  • Not known

Standard values

Children

Age Normal value in g/dL (♀/♂)
1. LM 4,2-6,2/4,1-6,3
1ST LM. – <6. LM 4,4-6,6/4,7-6,7
6. LM – < 12. LM 5,6-7,9/5,5-7,0
1. LJ – < 18. LJ 5,7-8,0/5,7-8,0

LM: month of life LY: year of life

Adult

Normal value in g/dl 6,1-8,1

Indications

  • Suspected synthesis disorders
  • Suspicion of malnutrition
  • Suspicion of malabsorption disorders

Interpretation

Interpretation of Elevated Values Hyperproteinemias are relatively rare because when immunoglobulins increase, there is a compensatory decrease in albumin.

  • Chronic inflammatory diseases
  • Liver cirrhosis (connective tissue remodeling of the liver leading to functional impairment [albumin decrease is less than gamma globulin increase].
  • Waldenström’s disease (Synonym: Waldenström’s macroglobulinemia) – malignant (malignant) lymphoma disease; counted among the B-cell non-Hodgkin’s lymphomas; typical is an abnormal production of monoclonal immunoglobulin M (IgM) by the lymphoma cells (= monoclonal gammopathy type IgM); Form of paraproteinemia in which there is osteoporosis (bone loss) and episodic purpura (capillary bleeding); in contrast to plasmocytoma, neither osteolysis (bone loss) nor hypercalcemia (calcium excess) are observed.
  • Plasmocytoma (multiple myeloma) – systemic disease caused by the proliferation of plasma cells.
  • Pseudohyperproteinemia – this may be due primarily to dehydration (lack of fluid).

Interpretation of lowered values

Cause: usually albumin reduction – rare disorder of immunoglobulin synthesis.

  • Analbuminemia
    • Familial
    • Nephrotic syndrome – collective term for symptoms associated with various diseases of the glomerulus (renal corpuscles); symptoms include proteinuria (excretion of protein in urine) with protein loss greater than 1 g/m²/body surface/d; hypoproteinemia; peripheral edema due to hypalbuminemia of < 2.5 g/dl in serum; hyperlipoproteinemia (lipid metabolism disorder).
  • Synthesis disorder
    • Antibody deficiency syndrome
  • Protein malnutrition
    • Anorexia nervosa (anorexia)
    • Hunger states
    • Gastrointestinal tumors (neoplasms of the gastrointestinal tract), unspecified.
    • Deficiency dystrophy in children
  • Malabsorption syndrome
    • Disaccaridase deficiency – deficiency of sugar-cleaving enzymes.
    • Cystic fibrosis – congenital metabolic disease caused by the absence of a protein; it leads to increase in the viscosity of bodily secretions as well as pancreatic ( pancreas) dysfunction: 2% of children and 50% of adults have diabetes mellitus and the lack of pancreatic secretions causes chronic diarrhea (diarrhea), maldigestion, malnutrition and digestive disorders and underweight.
    • Food allergy or food intolerance
    • Selective immunoglobulin A (IgA) deficiency
    • Celiac disease (gluten-induced enteropathy) – chronic disease of the mucosa of the small intestine (small intestinal mucosa) due to hypersensitivity to the cereal protein gluten.
  • Protein loss syndrome
  • Pseudohypoproteinemia – shift in protein levels due to:
    • Infusion therapy
    • Polydipsia (excessive drinking)
    • Pregnancy
  • Other causes
    • Ascites (abdominal dropsy)
    • Hemodialysis (blood washing)
    • Pleural exudate – effusion in the area between the pleura and the lung.