The Journal of Thoracic and Cardiovascular Surgery
Volume 140, Issue 1 , Pages 144-149, July 2010

Genetic factors are important determinants of impaired growth after infant cardiac surgery

  • Nancy Burnham, RN, MSN, CRNP

      Affiliations

    • Division of Cardiothoracic Surgery, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
    • Corresponding Author InformationAddress for reprints: Nancy Burnham, RN, MSN, CRNP, Division of Cardiothoracic Surgery, the Children's Hospital of Philadelphia, 34th and Civic Center Blvd, Philadelphia, PA 19104.
  • ,
  • Richard F. Ittenbach, PhD

      Affiliations

    • Division of Biostatistics and Epidemiology and the Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
  • ,
  • Virginia A. Stallings, MD

      Affiliations

    • Division of Gastroenterology, Hepatology and Nutrition, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
  • ,
  • Marsha Gerdes, PhD

      Affiliations

    • Division of Psychology, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
  • ,
  • Elaine Zackai, MD

      Affiliations

    • Division of Genetics, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
  • ,
  • Judy Bernbaum, MD

      Affiliations

    • Division of Pediatrics, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
  • ,
  • Robert R. Clancy, MD

      Affiliations

    • Division of Neurology, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa
  • ,
  • J. William Gaynor, MD

      Affiliations

    • Division of Cardiothoracic Surgery, the Cardiac Center, the Children's Hospital of Philadelphia, Philadelphia, Pa

Received 26 May 2009; received in revised form 16 November 2009; accepted 10 January 2010. published online 12 April 2010.

Objectives

We sought to estimate the prevalence and identify the predictors of impaired growth after infant cardiac surgery.

Methods

We performed a secondary analysis of a prospective study of the role of apolipoprotein E gene polymorphisms on neurodevelopment in young children after infant cardiac surgery. Prevalence estimates for growth velocity were derived by using anthropometric measures (weight and head circumference) obtained at birth and at 4 years of age. Genetic evaluation was also performed. Growth measure z scores were calculated by using World Health Organization Child Growth Standards. Growth velocity was evaluated by using 2 different techniques: first by clustering the children into one of 3 growth velocity subgroups based on z scores (impaired growth, difference < −0.5 standard deviation; stable growth, difference of −0.5 to 0.5 standard deviation; and improving growth, difference > 0.5 SD) and second by using continuous difference scores. Statistical analyses were conducted with a combination of proportional odds models for the ordered categories and simple linear regression for the continuous outcomes.

Results

Three hundred nineteen full-term subjects had complete anthropometric measures for weight and head circumference at birth and 4 years. The cohort was 56% male. Genetic examinations were available for 97% (309/319) of the cohort (normal, 74%; definite or suspected genetic abnormality, 26%). Frequency counts for weight categories were as follows: impaired growth, 37%; stable growth, 31%; and improving growth, 32%. Frequency counts for head circumference categories were as follows: impaired growth, 39%; stable growth, 28%; and improving growth, 33%. The presence of a definite or suspected genetic syndrome (P = .04) was found to be a predictor of impaired growth for weight but not for head circumference. When growth z scores were used as continuous outcomes, the apolipoprotein E ε2 allele was found to be predictive of lower z scores for both weight (P = .02) and head circumference (P = .03).

Conclusions

Impaired growth for both weight and head circumference is common (both >30%) in this cohort of children after infant cardiac surgery. Both the apolipoprotein E ε2 allele and the presence of a definite or suspected genetic syndrome were associated with impaired weight growth velocity. The apolipoprotein E ε2 allele was also associated with impaired growth velocity for head circumference. Persistent poor growth might have long-term implications for the health and development of children with congenital heart defects.

CTSNet classification: 20, 21

Abbreviations and Acronyms: APOE, apolipoprotein E, CHD, congenital heart defect, DHCA, deep hypothermic circulatory arrest, HC, head circumference, HCZ, head circumference–for–age z score, SD, standard deviation, TOF, tetralogy of Fallot, VSD, ventricular septal defect, WAZ, weight-for-age z score, WHO, World Health Organization

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 Supported by a grant from the Fannie E. Rippel Foundation, an American Heart Association National Grant-in-Aid (9950480N), and grant HL071834 from the National Institutes of Health.

 Disclosures: None.

PII: S0022-5223(10)00026-7

doi:10.1016/j.jtcvs.2010.01.003

The Journal of Thoracic and Cardiovascular Surgery
Volume 140, Issue 1 , Pages 144-149, July 2010