{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,23]],"date-time":"2025-09-23T13:49:16Z","timestamp":1758635356082},"reference-count":50,"publisher":"American Physiological Society","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Physiological Genomics"],"published-print":{"date-parts":[[2009,9]]},"abstract":"<jats:p> Goto-Kakizaki (GK) rats develop early-onset type 2 diabetes (T2D) symptoms, with signs of diabetic nephropathy becoming apparent with aging. To determine whether T2D and renal disease share similar genetic architecture, we ran a quantitative trait locus (QTL) analysis in the F2 progeny of a GK \u00d7 Brown Norway (BN) rat cross. Further, to determine whether genetic components change over time, we ran the QTL analysis on phenotypes collected longitudinally, at 3, 6, 9 and 12 mo, from the same animals. We confirmed three chromosomal regions that are linked to early diabetes phenotypes (chromosomes 1, 5, and 10) and a single region involved in the late progression of the disorder (chromosome 4). A single region was identified for the onset of the renal phenotype proteinuria (chromosome 5). This region overlaps the diabetic QTL, although it is not certain whether similar genes are involved in both phenotypes. A second QTL linked to the progression of the renal phenotype was found on chromosome 7. Linkage for triglyceride and cholesterol levels were also identified (chromosomes 7 and 8, respectively). These results demonstrate that, in general, different genetic components control diabetic and renal phenotypes in a diabetic nephropathy model. Furthermore, these results demonstrate that, over time, different genetic components are involved in progression of disease from those that were involved in disease onset. This observation would suggest that clinical studies collecting participants over a wide age distribution may be diluting genetic effects and reducing power to detect true effects. <\/jats:p>","DOI":"10.1152\/physiolgenomics.90389.2008","type":"journal-article","created":{"date-parts":[[2009,7,8]],"date-time":"2009-07-08T03:08:56Z","timestamp":1247022536000},"page":"38-46","source":"Crossref","is-referenced-by-count":16,"title":["Distinct genetic regulation of progression of diabetes and renal disease in the Goto-Kakizaki rat"],"prefix":"10.1152","volume":"39","author":[{"given":"Marcelo A.","family":"Nobrega","sequence":"first","affiliation":[{"name":"Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin"},{"name":"Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin"}]},{"given":"Leah C.","family":"Solberg Woods","sequence":"additional","affiliation":[{"name":"Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin"},{"name":"Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin"}]},{"given":"Stewart","family":"Fleming","sequence":"additional","affiliation":[{"name":"Department of Pathology, University of Dundee, Dundee, United Kingdom"}]},{"given":"Howard J.","family":"Jacob","sequence":"additional","affiliation":[{"name":"Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin"},{"name":"Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, Wisconsin"}]}],"member":"24","reference":[{"key":"R1","doi-asserted-by":"publisher","DOI":"10.2337\/db07-1059"},{"key":"R2","doi-asserted-by":"publisher","DOI":"10.1007\/BF00262007"},{"key":"R3","doi-asserted-by":"publisher","DOI":"10.1016\/0003-2697(76)90527-3"},{"key":"R4","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.26.7.2150"},{"key":"R5","doi-asserted-by":"publisher","DOI":"10.1038\/ng1796"},{"key":"R6","doi-asserted-by":"publisher","DOI":"10.1007\/s00335-005-0168-y"},{"key":"R7","doi-asserted-by":"publisher","DOI":"10.1086\/302316"},{"key":"R8","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.21.11.1932"},{"key":"R9","doi-asserted-by":"publisher","DOI":"10.1038\/nrg2178"},{"key":"R10","doi-asserted-by":"publisher","DOI":"10.1038\/ng0196-31"},{"key":"R11","doi-asserted-by":"publisher","DOI":"10.1097\/01.ASN.0000060572.13794.58"},{"key":"R12","doi-asserted-by":"publisher","DOI":"10.1038\/ng0196-38"},{"key":"R13","doi-asserted-by":"crossref","unstructured":"Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamaki K, Chines P, Balow J Jr, Birznieks G, Chang J, Eldridge W, Erdos MR, Karanjawala ZE, Knapp JI, Kudelko K, Martin C, Morales-Mena A, Musick A, Musick T, Pfahl C, Porter R, Rayman JB. 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