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Articles |
1
Department of Clinical Biochemistry, Odense University Hospital, DK-5000 Odense C, Denmark.
2
The Danish Center for Demographic Research and
Epidemiology, Institute of Public Health, University of Southern
Denmark, Main Campus: Odense University, DK-5000 Odense, Denmark.
3
Terry Sanford Institute, Duke University, Durham, NC
27708-0245.
4
Max Planck Institute for Demographic Research, Rostock
D-18057, Germany.
a Address correspondence to this author at: Department of Clinical Biochemistry, Odense University Hospital, DK-5000 Odense C, Denmark. Fax 45-6541-1911;
Lise.Bathum{at}ouh.fyns-amt.dk.
Background: Biochemical liver function tests are widely used in the clinic and are some of the most frequently used tests in screening for diseases in older age groups. The aim of the present study was to estimate the relative importance of genetic and environmental factors to variations in these tests among the elderly.
Methods: We conducted a survey among Danish twins, 73102 years
of age, identified in the population-based Danish Twin Registry. Among
the 2749 individuals in the study population, an interview was
conducted with 79%. From these, a blood sample was collected from 290
same-sex twin pairs, total of 580 subjects, within a 6-month period and
analyzed for alanine aminotransferase (ALT), lactate dehydrogenase
(LDH),
-glutamyltransferase (GGT), bilirubin, and albumin. The
interview included questions about alcohol consumption and body mass
index (BMI; self-calculated height and weight). Heritability
(proportion of the population variance attributable to genetic
variation) was estimated using structural-equation analyses before and
after correction for alcohol consumption and BMI.
Results: Structural-equation analyses revealed a substantial heritability (3561%) for the four biochemical liver function tests: ALT, GGT, LDH, and bilirubin. The remaining variation could be attributed to individuals nonfamilial environments. Adjustment for alcohol consumption and BMI had no influence on the heritability for ALT, GGT, LDH, and bilirubin. For albumin, two models fit equally well before adjustment for alcohol and BMI: a model including additive genetic and nonshared environmental factors (AE), and a model including shared and nonshared environmental factors (CE). After adjustment, the model including shared and nonshared environment was clearly the best fitting model.
Conclusions: For both males and females, the effect of genetic factors on the biochemical liver function tests ALT, GGT, LDH, and bilirubin is substantial and accounts for one-third to two-thirds of the variation among individuals 73102 years of age. The heritability is equal for males and females and does not change notably after controlling for alcohol consumption and BMI. For albumin, no major impact of genetic factors was found independent of BMI and alcohol consumption. An understanding of the genetic mechanisms underlying biochemical liver function tests among the very old may be of value in the interpretation of these tests in this age group.
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