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Population-based studies have used DNA typing of Mycobacterium tuberculosis organisms to estimate the extent of ongoing tuberculosis transmission in various communities and to characterize associated risk factors. The finding of matched DNA “fingerprints” among isolates from an immigrant subgroup may reflect transmission in the adopted country but could also reflect limited diversity among M. tuberculosis organisms within that immigrant community. The authors sought to determine which hypothesis is more likely to explain the high frequency of matched isolates among Haitian-born tuberculosis patients in Montreal, Quebec, Canada. The authors determined the number of different bacterial genotypes in this community as compared with other foreign-born tuberculosis patients and applied a recently described measure of genetic similarity between M. tuberculosis organisms (“genetic distance”). Among 76 Haitian-born tuberculosis patients diagnosed during 1996–1998, the authors identified 47 distinct genotypes on the basis of standard IS6110 DNA typing and categorical analysis. In genetic distance analysis, these 47 genotypes showed as great a genetic diversity as that observed among the 191 distinct genotypes identified in 216 other foreign-born tuberculosis patients. A mycobacterial “founder effect” is unlikely to account for the high proportion of shared isolates among Haitian-born Montrealers. Recent transmission remains the most likely explanation. [ABSTRACT FROM AUTHOR]

In a previous cross-sectional study of twins, the authors found evidence of a substantial genetic influence on functional abilities among elderly women. It has been suggested that rate of change in functional abilities over time could underlie such findings and that rate-of-change phenotypes may have an even larger genetic component than “level” phenotypes (e.g., functional abilities per se). If so, rate-of-change phenotypes could be more powerful than level phenotypes in studies aimed at identifying specific polymorphisms of importance for aging. In 1995, the authors assessed a population-based sample of 2,401 Danish twins aged 75 years or more. The survivors were recontacted after 2 years and again after 4 years. Consistent mean-level declines, high within-person correlations over time, and substantial heritability in the female sample were observed for functional abilities. Nonetheless, structural-equation analyses revealed only a very modest and nonsignificant heritability for rate of change in functional abilities: 16% (95% confidence interval: 0, 35) for women and 9% (95% confidence interval: 0, 44) for men. This study had a large initial sample size, high participation rates, and a valid and reliable measure of rate of change in a phenotype that had previously shown substantial heritability in cross-sectional analyses in the same twin population. Still, the present study revealed only a modest and nonsignificant genetic influence on rate of change, which suggests that detection of polymorphisms influencing rate of change in functional abilities among the elderly may prove to be difficult. [ABSTRACT FROM PUBLISHER]

Lean mass and areal bone mineral density at the lumbar spine, femoral neck, and total forearm were measured in 215 volunteer female twin pairs (122 monozygotic, 93 dizygotic), aged 10–26 years, using dual energy X-ray absorptiometry. The study was conducted in Melbourne from 1990 to 1994. Under the classic twin model, there was evidence for a genetic component of variation in bone mineral density, adjusted for age or for age and lean mass, at all sites. Adjusting for lean mass almost halved the genetic variances in the adolescent years of peak growth, during which genetic variances peaked. Genetic variances were reduced in the late teenage years and increased in early adulthood. The latter may reflect gene-environment interactions or covariation. Importantly, there was evidence for environmental effects shared by twins on lumbar spine and femoral neck bone mineral density, even when adjusted for lean mass as well as age. These were greatest during the late teenage years, abated over the years when pairs started to live apart, and appear to be independent of lean mass during adolescence but not in early adulthood. In summary, the genetic and environmental etiology of bone mineral density is more complex than previously thought. [ABSTRACT FROM AUTHOR]