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    ABC series from the BMJABC of Monitoring Drug Therapy. By ]. K. Aronson, M. Hardman and D. J. M. Reynolds. Pp. ix + 38. Illustrated. £9. BM]. 1993. (ABC books are available through the Book Division, MASA Publications, tel. (021) 531-3081.) ISBN 0-7279-0791-3.ABC of AIDS. 3rd ed. Ed. by Michael Wadler. Pp. 86. Illustrated. £15. BM]. 1993. ISB T 0-7279-0761-1.ABC of Dermatology. 2nd ed. By P. K. Buxton. Pp. 98. Illustrated. £15. BM]. 1993. ISBN 0-7279-0777-8.ABC of Healthy Travel 4th ed. By Eric Walker, Glyn Williams and Fiona Raeside. Pp. 49. Illustrated. £12. BM]. 1993. ISBN 0-7279-0762-X.ABC of Otolaryngology. 3rd ed. By Harold Ludman. Pp. 58. Illustrated. £11. BM]. 1993. ISH- T 0-7279-0765-4.ABC of Colorectal Diseases. Ed. by D. ]. Jones and M. H. Irving. Pp. 103. Illustrated. £15. BM]. 1993. ISBN 07279- 9755-7.Tissue bankingMusculoskeletal Tissue Banking. By William W. Tornford (with contributions by James H. Forsell, Allen P. MacKenzie and D. Michael Stron). Pp. xiii + 240. Illustrated.94,50. Raven Press. 1993. ISBN 0-88167-995-X.Tobacco smokingLegislative Action to COIIlbat the World Tobacco Epidemic. 2nd ed. R. Roemer. pp. xiii + 297. SFr.59. in developing counrries: SFr.41,30. WHO. 1993. ISBN 92-4156157-2.There's Sunlight in My Leaf. Biography of Nicotiana tabacum. By Johan Fourie. Pp. 69. Marius du Plooy Communications. 1992. ISBN 0-620-17064-6.NutritionFood, Facts and Figures. The Complete South African Guide. Pp. 135. Illustrated. RI9,99. Oxford University Press (In collaboration with the Medical Research Council). 1992. ISBN 0-19-570736-2.OrthopeadicsOrthopaedic Diagnosis and ManagelDent: A Guide to the Care of Orthopaedic Patients. By Boyd S. Goldie. Pp. xviii + 247. £17,95. Blackwell Scientific Publications.1992. ISBN 0-632-03043-7.Biliary stonesBailliere's Clinical Gastroenterology. International Practice and Research. Diagnosis and Management of Biliary Stones. Ed. by M. Sackmann. Pp. x + 200. lllustrated. £27,50. Harcourt Brace Jovanovich. 1992. ISBN 0-7020-1 625-X.Molecular and cell biologyBasic Molecular and Cell Biology. 2nd ed. Pp. vii + 209. illustrated. BM}. 1993. ISBN 0-7279-0772-7.Nutritional anaemiasNutritional Anaemias. Nestle Nutritional Workshop Series. Vol. 30. Ed by Samuel }. Fomon and Stanley Zlotkin. Pp. xii + 220. 75. New York: Raven Press. 1992

    Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults

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    BACKGROUND: suPAR (Soluble urokinase plasminogen activator receptor) has emerged as an important biomarker of coagulation, inflammation, and cardiovascular disease (CVD) risk. The contribution of suPAR to CVD risk and its genetic influence in Black populations have not been evaluated. METHODS: We measured suPAR in 3492 Black adults from the prospective, community-based JHS (Jackson Heart Study). Cross-sectional associations of suPAR with lifestyle and CVD risk factors were assessed, whole-genome sequence data were used to evaluate genetic associations of suPAR, and relationships of suPAR with incident CVD outcomes and overall mortality were estimated over follow-up. RESULTS: In Cox models adjusted for traditional CVD risk factors, estimated glomerular filtration rate, and CRP (C-reactive protein), each 1-SD higher suPAR was associated with a 21% to 31% increased risk of incident coronary heart disease, heart failure, stroke, and mortality. In the genome-wide association study, 2 missense (rs399145 encoding p.Thr86Ala, rs4760 encoding p.Phe272Leu) and 2 noncoding regulatory variants (rs73935023 within an enhancer element and rs4251805 within the promoter) of PLAUR on chromosome 19 were each independently associated with suPAR and together explained 14% of suPAR phenotypic variation. The allele frequencies of each of the four suPAR-associated genetic variants differ considerably across African and European populations. We further show that PLAUR rs73935023 can alter transcriptional activity in vitro. We did not find any association between genetically determined suPAR and CVD in JHS or a larger electronic medical record-based analyses of Blacks or Whites. CONCLUSIONS: Our results demonstrate the importance of ancestry-differentiated genetic variation on suPAR levels and indicate suPAR is a CVD biomarker in Black adults
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