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ESI Special Topic: Polybrominated Diphenyl Ethers
Publication Date: August 2007

Polybrominated Diphenyl Ethers

ESI Special Topics: September 2007
Citing URL: http://esi-topics.com/pbde/interviews/AkeBergman.html

An INTERVIEW with Dr. Åke Bergman
According to our Special Topics analysis on PBDE research over the past decade, Dr. Åke Bergman's work ranks at the top, with 49 papers cited a total of 1,622 times. In Essential Science IndicatorsSM, Dr. Bergman's work can be found in the fields of Environment & Ecology and Pharmacology & Toxicology, and includes 210 papers cited a total of 3,889 times to date. Dr. Bergman is the Chair of the Department of Environmental Chemistry at Stockholm University in Sweden. In the interview below, he talks with correspondent Gary Taubes about his highly cited PBDE research.

ST:  When did you first start working on PBDEs?

I have a fairly long history in environmental research, studying organic environmental contaminants, going back to my doctoral work in the second part of the 1970s. Accordingly it was natural to come across PBDEs after their discovery in Swedish wildlife in 1981. In 1989, the Swedish Chemical Agency hosted a meeting on brominated flame retardants, and I knew when we first discussed it, that we needed to do chemical synthesis to get reference compounds. It’s almost impossible to do anything unless you have a pure standard to work with, and that goes both for the analytical and toxicological work. It was obvious that pure standards were required for the PBDEs, just as it had been for the PCBs and PCB metabolites that I had worked with up till then.

ST:  How did you approach the problem after that 1989 meeting?

At the end of the meeting, it was really up to me as a scientist to decide if this was something I wanted to do. There was no grant money available at that time but some pressure from colleagues that I should give it a try. I was able to receive some financial support, so we slowly started to dig into the chemical synthesis of individual compounds. Theoretically, PBDEs can consist of up to 209 different chemical compounds but the knowledge on commercial mixture compositions of PBDEs was rudimentary. We knew the structure of one of the PBDE compounds; that was it.

 

“Theoretically, PBDEs can consist of up to 209 different chemical compounds but the knowledge on commercial mixture compositions of PBDEs was rudimentary.”

 

So we started doing chemical synthesis and we have continued to do so up till today. It has been a matter of finding the best methodology for synthesis of pure PBDE compounds, to refine or come up with new ideas how to prepare them. When we had a reasonable number of pure standards available they could then be used as analytical standards. One of our papers that is still highly cited reports the outcome of this work. It was, for example, possible to assess PBDEs in milk from nursing women in Stockholm (Meironyte D, et al., "Analysis of polybrominated diphenyl ethers in Swedish human milk. A time-related trend study, 1972-1997," J. Toxicol. Env. Health A 58:329-41, 1999). The result of that study showing increasing levels of PBDEs with time, redoubling every fifth year, was presented at the annual Dioxin conference in 1998.

ST:  The mothers’ milk study is your second most-cited paper. What made so influential?

The report was shocking, instead of declining concentrations of environmental contaminants like DDTs, PCBs and other POPs, the PBDEs were indeed showing the reverse temporal trend in the mothers’ milk. This was really new to everyone—to scientists, authorities, and the public. The data showed, independent of what we all thought at the time, that the society had a fair control over persistent contaminants. Indeed, our data was confirmed in other studies in wildlife and other environmental matrices.

ST:  Your most-cited paper is the 2000 Toxicological Sciences paper, "Potent competitive interactions of some brominated flame retardants and related compounds with human transthyretin in vitro," (Meerts IATM, et al. 56[1]: 95-104, July 2000). What was that about and why do you think it’s been cited so frequently?

That paper was the natural next step in this process: after some initial analytical work was done, we want to know what the effects are. It was obvious from the structures of PBDEs that they do indeed have a structural resemblance to thyroxin, the thyroid hormone. Meerts, the first author, was a doctoral student at Wageningen University (The Netherlands), and we supplied her with the necessary chemicals in order to test endocrine effects of PBDEs. This paper reports on the metabolism of PBDEs to hydroxylated PBDEs, and on competition studies between thyroxin on one side and PBDE congeners, PBDEs after microsomal transformations and a few synthetic hydroxylated PBDEs (OH-PBDEs) on the other, for the transport protein transthyretin.

ST:  So why do you think it’s been cited so often?

I don’t know for sure, but it was indeed the first study to report on strong binding potencies to transthyretin. The paper is dealing PBDEs and their potential for inducing endocrine effects and that is a hot topic. The paper was among the first to address toxicological effects of PBDEs and this is always a key issue in research on environmental contaminants.

ST:  You have remained in the forefront of PBDE research for over a decade, but you seem to collaborate widely. How important are these collaborations to doing what you do?

This has never been work to be done all by myself. I may have been a researcher that fused the escalation of the research interest in PBDEs, but much of the success is through collaborations. I have been fortunate to have strong and good collaborators in Sweden, Europe, North America, and Japan covering a variety of scientific areas. This is not the least important in the area of toxicokinetics, making metabolism research a key in what I have been involved in. Through collaborations in an interdisciplinary way, it has been possible to achieve data on PBDE half-lives and lot of exposure assessments in people around the world. Frighteningly high concentrations of PBDEs have been observed not only in U.S. adults but also in children in the U.S. and in Nicaragua. This is of particular concern to me.

ST:  What have you learned about PBDEs in the last decade of research and how has that affected how your own research has evolved?

Since 1998, there’s been an exponential increase in research worldwide on PBDEs, both regarding effects and exposure assessments and in wildlife and humans. What I have actually done recently is taken the step to the next phase, and now I’m much more interested in PBDE metabolites—in hydroxylated PBDEs that we have actually found in humans. We also have linked these metabolites to naturally produced compounds that are very, very similar to hydroxylated PBDE metabolites. So I’m leaving the PBDE exposure assessments. I think that work is basically finished. Now I’m trying to continue and move on to new areas. At least, I am striving to be ahead of the front in BFR research.

ST:  What has proven to be the biggest obstacle to successful research on PBDEs?

The chemical synthesis—to get the pure compounds we need for analytical assessment was a major obstacle. We had to invest a lot of energy to do the chemical synthesis, to find the right methodology for PBDE congener synthesis in the past; nowadays we are looking into synthesis of PBDE metabolites. What the commercial companies offering analytical standards are now using is our methodology to produce these PBDE compounds. That is a satisfying achievement, I think.

Of course, I would still like to see more research on the effects side. Although this is a typical picture in this kind of work. The chemical area, the exposure assessments, comes first and dominates the scientific publications, then comes the research on toxicological effects. I would like to see more structured work on testing individual PBDE compounds (as chemicals in general). We need better interdisciplinary cooperation to achieve more. And, of course, money is the real big obstacle. In the U.S., there has been extremely little money allocated for PBDE research. In Europe it’s been better. But you can’t achieve very much without money.

ST:  If you were in charge of funding in this research, how would you allocate it?

I would definitely want to set up a program to look much more at the unknowns. I would actually allocate less money to PBDEs because we have a pretty good idea what’s going on there; there has been so much research for a long time. Instead, I’d like to look at the other compounds, particularly focusing on those compounds that are now replacing PBDEs in flame retardants. Some of these alternative flame retardants are brominated, and that’s what we need to focus on. Look at these compounds that we know very little about—maybe synthesize them and make it possible to go back and do toxicological assessments.End

Åke Bergman, Ph.D.
Department of Environmental Chemistry
Stockholm University
Stockholm, Sweden

Dr. Åke Bergman's most-cited paper with 194 cites to date:
Brouwer A, et al., "Interactions of persistent environmental organohalogens with the thyroid hormone system: mechanisms and possible consequences for animal and human health," Toxicol. Ind. Health 14(1-2): 59-84, Jan-Apr 1998.

Three of Dr. Bergman's papers are also represented in the Research Front map.

Source: Essential Science Indicators.


Related Links:
Dr. Åke Bergman is featured in ISIHighlyCited.com

ESI Special Topics: September 2007
Citing URL: http://esi-topics.com/pbde/interviews/AkeBergman.html

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