Prevalence of Monoclonal Gammopathy of Undetermined Significance Among Men in Ghana

Ola Landgren, Jerry A. Katzmann, Ann W. Hsing, Ruth M. Pfeiffer, Robert A. Kyle, Edward D. Yeboah, Richard B. Biritwum, Yao Tettey, Andrew A. Adjei, Dirk R. Larson, Angela Dispenzieri, L. Joseph Melton, Lynn R. Goldin, Mary L. McMaster, Neil E. Caporaso, S. Vincent Rajkumar

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

OBJECTIVES To determine the prevalence of monoclonal gammopathy of undetermined significance (MGUS), a precursor of multiple myeloma (MM), in Ghanaian men vs white men and to test for evidence to support an underlying race-related predisposition of the 2-fold higher prevalence of MGUS in African Americans vs whites. PARTICIPANTS AND METHODS Between September 1, 2004, and September 30, 2006, 917 men (50-74 years) underwent in-person interviews and physical examinations. Serum samples from all participants were analyzed by electrophoresis performed on agarose gel; any serum sample with a discrete or localized band was subjected to immunofixation. Age-adjusted and standardized (to the 2000 world population) prevalence estimates of MGUS and 95% confidence intervals (CIs) were computed in the Ghanaian men and compared with MGUS prevalence in 7996 white men from Minnesota. Associations between selected characteristics and MGUS prevalence were assessed by the Fisher exact test and logistic regression models. RESULTS Of the 917 study participants, 54 were found to have MGUS, yielding an age-adjusted prevalence of 5.84 (95% CI, 4.27-7.40) per 100 persons. No significant variation was found by age group, ethnicity, education status, or prior infectious diseases. The concentration of monoclonal immunoglobulin was undetectable in 41 (76%) of the 54 MGUS cases, less than 1 g/dL in 10 patients (19%), and 1 g/dL or more in only 3 patients (6%). Compared with white men, the age-adjusted prevalence of MGUS was 1.97-fold (95% CI, 1.94-2.00) higher in Ghanaian men. CONCLUSION The prevalence of MGUS in Ghanaian men was twice that in white men, supporting the hypothesis that race-related genetic susceptibility could explain the higher rates of MGUS in black populations. An improved understanding of MGUS and MM pathophysiology would facilitate the development of strategies to prevent progression of MGUS to MM.

Original languageEnglish (US)
Pages (from-to)1468-1473
Number of pages6
JournalMayo Clinic proceedings
Volume82
Issue number12
DOIs
StatePublished - Dec 2007

Keywords

  • CI
  • MGUS
  • MM
  • confidence interval
  • monoclonal gammopathy of undetermined significance
  • multiple myeloma

ASJC Scopus subject areas

  • General Medicine

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