Genetic Effects on Baseline Values of C-Reactive Protein and Serum Amyloid A Protein: A Comparison of Monozygotic and Dizygotic Twins

• Published in: Clinical chemistry (Baltimore, Md.) Vol. 50; no. 1; pp. 130 - 134
• Main Authors: MacGregor, Alex J, Gallimore, J. Ruth, Spector, Tim D, Pepys, Mark B
• Format: Journal Article
• Language: English
• Published: Washington, DC Am Assoc Clin Chem 01.01.2004; American Association for Clinical Chemistry; Oxford University Press
• Subjects: Adult; Aged; Angina pectoris; Autoanalysis; Automation; Biological and medical sciences; Blood & organ donations; Blood pressure; Body mass index; C-Reactive Protein - analysis; C-Reactive Protein - genetics; Confounding (Statistics); Disease; Enzymes; Female; Fundamental and applied biological sciences. Psychology; Genetic effects; Genetic engineering; Hormone replacement therapy; Humans; Immunoassay; Immunoassays; Immunoenzyme Techniques; Investigative techniques, diagnostic techniques (general aspects); Medical sciences; Middle Aged; Molecular and cellular biology; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Proteins; Reference Values; Serum Amyloid A Protein - analysis; Serum Amyloid A Protein - genetics; Statistical models; Twins; Twins, Dizygotic; Twins, Monozygotic; World Health Organization; United Kingdom > UK; Serum amyloid protein SAA; Acute phase protein; Clinical biology; Dizygotic twin; Value; Genetics; Biochemistry; C reactive protein; Serum protein; Monozygotic twin; Comparative study
• ISSN: 0009-9147; 1530-8561
• DOI: 10.1373/clinchem.2003.028258

C-Reactive protein (CRP) and serum amyloid A protein (SAA) are exquisitely sensitive acute-phase reactants, but their baseline values are surprisingly constant in individuals in the general population. These values, especially of CRP, are associated with future atherothrombotic events, and the determinants of baseline CRP and SAA concentration are therefore of considerable interest. CRP and SAA concentrations were measured by well-validated automated microparticle capture enzyme immunoassays, standardized on the respective WHO International Reference Standards, in serum from 146 monozygotic and 164 dizygotic healthy female UK twin pairs from the general population, with mean (range) ages of 58.0 (40-69.6) and 55.7 (40-70.3) years, respectively, who were also very closely matched for height, weight, body mass index, blood pressure, and lifestyle variables. Statistical modeling based on variance components analysis was used to estimate the genetic contribution to the observed values. As reported previously, CRP values were associated with body mass index, smoking, and hormone replacement therapy. After exclusion of the few samples with CRP concentrations >10 mg/L, which indicate an ongoing acute-phase response rather than baseline values, and inclusion of adjustments for all known confounding variables, there was significantly higher correlation of CRP and SAA results among monozygotic than among dizygotic twins. The estimated hereditability (95% confidence interval) of baseline values was 52% (40-62%) for CRP and 59% (49-67%) for SAA. There is a substantial genetic contribution to baseline serum concentrations of CRP and SAA.