Donald S. Fredrickson

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Donald S. Fredrickson in 1961
Donald S. Fredrickson in 1961

Donald Sharp "Don" Fredrickson (August 8, 1924 - June 7, 2002) was an American medical researcher, principally of the lipid and cholesterol metabolism, and director of National Institutes of Health and subsequently the Howard Hughes Medical Institute.[1]

Contents

[edit] Biography

Fredrickson was born in Canon City, Colorado. His father was a lawyer. After high school he commenced medical school at the University of Colorado, but completed his studies at the University of Michigan after being transferred there by the army. During a cycling trip in the Netherlands he met his future wife, Priscilla Eekhof, and they married two years later. They would have two sons.[1]

Between 1949 and 1952 he worked as a resident and subsequently as a fellow in internal medicine at the Peter Bent Brigham Hospital (now part of Brigham and Women's Hospital) in Boston. Much of his published work from this period is in the field of endocrinology. Subsequently he spent a year in the laboratory of Ivan Frantz, a cholesterol biochemist, at Massachusetts General Hospital.[1]

[edit] Lipid research

In 1953 he took up a post at the National Heart Institute, part of the National Institutes of Health in Bethesda, Maryland. Initially, he worked with protein chemist and Nobel laureate Christian B. Anfinsen, and subsequently (with Daniel Steinberg) developed an interest in the metabolism of cholesterol and lipoproteins, as well as related medical conditions such as Niemann-Pick disease. His group identified Tangier disease (HDL deficiency)[2] and cholesteryl ester storage disease, two inborn errors of cholesterol metabolism. He played a prime role in the identification of several apolipoproteins (proteins that characterise the nature of a blood lipid particle): APOA2, APOC1, APOC2 and APOC3.[1]

In 1967 Fredrickson co-authored the paper that described the classification of lipoprotein abnormalities in five types, depending on the pattern of lipoprotein electrophoresis; this became known as the Fredrickson classification.[3] It was adopted as the mondial standard by the World Health Organization in 1972.[1] His group also conducted the first trials of pharmacological cholesterol reduction in the prevention and treatment of cardiovascular disease.[1]

[edit] Textbooks

From 1960 he worked, with John Stanbury and James Wyngaarden, on several editions of the encyclopedic medical textbook The Metabolic and Molecular Bases of Inherited Disease.[4][1]

[edit] Directorships

Apart from his work in research, Fredrickson was involved in the management of the NHI from an early stage. He was clinical director from 1960 onward and from 1966 general director of NHI. In 1974 he left the NHI (then already the National Heart and Lung Institute) to head the Institute of Medicine of the National Academy of Sciences. Nine months later he was asked by president Gerald Ford to become head of the National Institutes of Health, a task he commenced on 1975-06-01.[1]

One of the main issues that occupied him was the controversy over research involving recombinant DNA. Already in 1973 there had been scientists urging a ban on such research for environmental reasons. Fredrickson released a guideline that restricted release of genetically modified organisms into the environment, and called into existence a body that would advise on these matters and had to approve any NIH research involving recombinant DNA technology. Fredrickson is credited with restoring confidence in this form of research.[1] A second controversy involved congressional control over the NIH in general. Some feel that Fredrickson's decision to resign from his position in 1981 was fuelled by these controversies.[1] The recombinant DNA controversy was the subject of a book published by Fredrickson in 2001.[5]

After 1981 Fredrickson was scholar-in-residence at the National Academy of Sciences for two years, but in 1983 he was recruited to become the vice-president of the Howard Hughes Medical Institute, a privately-run health research charity. At that stage, the institute was still the owner of the Hughes Aircraft Company, and Fredrickson participated in the negotiations that led to the sale (for $5.2 billion) to General Motors. He made substantial changes to the institute's research programme. He resigned in 1987 when the trustees of the institute discovered that there had been financial malversations under his presidency.[1]

[edit] Later years

Fredrickson returned to the NIH, resuming work on lipid diseases and writing for the National Library of Medicine. He participated in the genetic elucidation of Tangier disease, which he had himself described in the 1960s.[6][1]

He was personal physician to Hassan II of Morocco, and had a close personal friendship with the king until the latter's death in 1999.[1]

He was found dead, face-down, in his swimming pool in 2002. He is buried in Leiden, the Netherlands.[1]

[edit] References

  1. ^ a b c d e f g h i j k l m n Wyngaarden JB. "Donald Sharp Fredrickson". In Biographical Memoirs. National Academy of Sciences 2006;87:164-179. ISBN 0-309-09579-4. Fulltext. Reprinted from Proc Am Phil Soc 2004;148(3):382-393. PDF.
  2. ^ Fredrickson DS, Altrocchi PH, Avioli LV, Goodman DS, Goodman HC. Tangier disease. Ann Intern Med 1961;55:1016-1031.
  3. ^ Fredrickson DS, Levy RI, Lees RS. Fat transport in lipoproteins--an integrated approach to mechanisms and disorders. N Engl J Med 1967;276:34-42. PMID 5333081.
  4. ^ Stanbury JB, Wyngaarden JB, Fredrickson DS (Eds). The Metabolic Basis of Inherited Disease. New York, Toronto, and London: McGraw-Hill, 1960.
  5. ^ Fredrickson DS. The Recombinant DNA Controversy: A Memoir, Science, Politics, and the Public Interest 1974-1981. ASM press, 2001. ISBN 1-55581-222-8.
  6. ^ Remaley AT, Rust S, Rosier M, Knapper C, Naudin L, Broccardo C, Peterson KM, Koch C, Arnould I, Prades C, Duverger N, Funke H, Assman G, Dinger M, Dean M, Chimini G, Santamarina-Fojo S, Fredrickson DS, Denefle P, Brewer HB Jr. Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred. Proc Natl Acad Sci U S A 1999;96:12685-90. PMID 10535983.

[edit] External links