Quantitative Morphology in Kidney Research
February 13-14, 2012 Conference Videos

Conference Summary
Kevin Lemley, University of Southern California

Video Transcript

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KEVIN LEMLEY: So, my charge was to summarize the whole thing. No problem. I can only say one thing about John Bertram’s talk:

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when everybody gets back to your institution, go on the website and have everybody who has to do anything, look at it, maybe multiple times. I think

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Wendy might agree with this that it got harder to summarize people at the end, but unlike decreased glomerular number, which we’ve been

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thinking of for a while, that perhaps certainly decreased glomerular number related to how much work you have to do, how big you are, but

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also increased glomerular volume and increased glomerular volume heterogeneity may be very important parameters to pay attention to.

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Yesterday, before either Kevin or Norbert got a chance to do anything they were asked for multiple times, because people said over and over

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and over again, and again today, “What we really need is in vivo methods to estimate glomerular number and then we won’t have to see

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stereologists and model-based people doing battle all the time.” Just get the in vivos. Erwin showed us that there are some QTLs that may

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affect podocyte susceptibility to loss and also, I think, illustrated that some of these quantitative things may actually be very closely related as the

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discussion showed afterwards, and we need to be very clear on what we’re actually deducing from our data. Roger Wiggins gave a

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demonstration of another model-based method, essentially the XY version rather than the Z version of the thick-thin method, and therefore

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gave us one more thing to debate and try to validate or disvalidate against gold standard methods. Ms. Thompson from the FDA basically

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said that if we’re going to be trying to sell them reasonably likely surrogates we’d better have some common standard approaches, which

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probably makes sense, especially here in our discussions. Kevin Bennett showed some very interesting and suggestive data, and I should just

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kind of say that Norbert Gretz’s is the same type of thing: for MR, for ex vivo and hopefully soon, at least in animals, in vivo ways of developing

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estimators of at least glomerular number and maybe glomerular number and function together, which would be a great advance. We’ll be to that

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Star Trek scanner where we just scan someone and can tell everything about them. But more work is needed and, in particular, the challenges

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will probably be, if not proportional to body weight for humans versus rats, at least will be greater for humans than for rats and mice.

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Steven Hewitt pointed out something that we’ve only really had thrown in our face when trying to do the NEPTUNE, is that a lot of the things…there

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are some clear advantages to digital microscopy and virtual microscopy but there are probably at least as many challenges as are advantages and

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they have to be overcome. So, I would just like, myself, to thank Jeffrey for the huge amount of work he did putting this conference together on

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rather short notice, and I think it turned out quite well, and I’m happy to sign off.




Date Last Updated: 10/5/2012

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