Psoriasis and risk of chronic kidney diseases: A population-based cross-sectional study and Mendelian randomization analysis
Conflicting results have been reported regarding the association between psoriasis and risk of chronic kidney diseases (CKD). Furthermore, the causal nature of the possible association remains unexplored. We conducted a population-based cross-sectional study using data from National Health and Nutri...
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Veröffentlicht in: | Nephrology (Carlton, Vic.) Vic.), 2023-11, Vol.28 (11), p.611-619 |
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description | Conflicting results have been reported regarding the association between psoriasis and risk of chronic kidney diseases (CKD). Furthermore, the causal nature of the possible association remains unexplored.
We conducted a population-based cross-sectional study using data from National Health and Nutrition Examination Survey (NHANES). Logistic regression analyses were conducted to estimate potential association between psoriasis and CKD risk. Further, we evaluated causality by performing a Mendelian randomization analysis using large-scale genome-wide association studies of psoriasis and CKD. Inverse variance-weighted (IVW) analysis was used as the primary method.
In the observational study, 16 750 participants were included. Overall, 39 of 429 patients with psoriasis had CKD (9.1%) compared with 1481 of 16 321 without psoriasis (9.1%). In the fully adjusted model, psoriasis was not associated with CKD (OR: 0.77, 95%CI: 0.53-1.10). In the MR analysis, 36 single-nucleotide polymorphisms (SNPs) were selected as instrumental variables. The IVW analysis reported that genetically predicted psoriasis was associated with a higher risk of CKD (OR: 1.025, 95%CI: 1.001-1.049). After removing 2 SNPs associated with heterogeneity, the association remained (OR: 1.028, 95%CI: 1.006-1.050).
Genetically predicted psoriasis was associated with a higher risk of CKD. This association may be important for clinicians to monitor kidney function and prescribe potentially nephrotoxic drugs during psoriasis management. |
doi_str_mv | 10.1111/nep.14220 |
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We conducted a population-based cross-sectional study using data from National Health and Nutrition Examination Survey (NHANES). Logistic regression analyses were conducted to estimate potential association between psoriasis and CKD risk. Further, we evaluated causality by performing a Mendelian randomization analysis using large-scale genome-wide association studies of psoriasis and CKD. Inverse variance-weighted (IVW) analysis was used as the primary method.
In the observational study, 16 750 participants were included. Overall, 39 of 429 patients with psoriasis had CKD (9.1%) compared with 1481 of 16 321 without psoriasis (9.1%). In the fully adjusted model, psoriasis was not associated with CKD (OR: 0.77, 95%CI: 0.53-1.10). In the MR analysis, 36 single-nucleotide polymorphisms (SNPs) were selected as instrumental variables. The IVW analysis reported that genetically predicted psoriasis was associated with a higher risk of CKD (OR: 1.025, 95%CI: 1.001-1.049). After removing 2 SNPs associated with heterogeneity, the association remained (OR: 1.028, 95%CI: 1.006-1.050).
Genetically predicted psoriasis was associated with a higher risk of CKD. This association may be important for clinicians to monitor kidney function and prescribe potentially nephrotoxic drugs during psoriasis management.</description><identifier>ISSN: 1320-5358</identifier><identifier>EISSN: 1440-1797</identifier><identifier>DOI: 10.1111/nep.14220</identifier><identifier>PMID: 37469214</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Cross-sectional studies ; Genomes ; Kidney diseases ; Population studies ; Population-based studies ; Psoriasis ; Single-nucleotide polymorphism</subject><ispartof>Nephrology (Carlton, Vic.), 2023-11, Vol.28 (11), p.611-619</ispartof><rights>2023 Asian Pacific Society of Nephrology.</rights><rights>2023 Asian Pacific Society of Nephrology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-630c300841dc5678a49b303e467800da4886aca4b3efae550b1ea7f484a60aa43</citedby><cites>FETCH-LOGICAL-c348t-630c300841dc5678a49b303e467800da4886aca4b3efae550b1ea7f484a60aa43</cites><orcidid>0000-0001-9710-7872</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37469214$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yin, Saifu</creatorcontrib><creatorcontrib>Zhou, Zhaoxia</creatorcontrib><creatorcontrib>Wu, Jiapei</creatorcontrib><creatorcontrib>Wang, Xianding</creatorcontrib><creatorcontrib>Lin, Tao</creatorcontrib><title>Psoriasis and risk of chronic kidney diseases: A population-based cross-sectional study and Mendelian randomization analysis</title><title>Nephrology (Carlton, Vic.)</title><addtitle>Nephrology (Carlton)</addtitle><description>Conflicting results have been reported regarding the association between psoriasis and risk of chronic kidney diseases (CKD). Furthermore, the causal nature of the possible association remains unexplored.
We conducted a population-based cross-sectional study using data from National Health and Nutrition Examination Survey (NHANES). Logistic regression analyses were conducted to estimate potential association between psoriasis and CKD risk. Further, we evaluated causality by performing a Mendelian randomization analysis using large-scale genome-wide association studies of psoriasis and CKD. Inverse variance-weighted (IVW) analysis was used as the primary method.
In the observational study, 16 750 participants were included. Overall, 39 of 429 patients with psoriasis had CKD (9.1%) compared with 1481 of 16 321 without psoriasis (9.1%). In the fully adjusted model, psoriasis was not associated with CKD (OR: 0.77, 95%CI: 0.53-1.10). In the MR analysis, 36 single-nucleotide polymorphisms (SNPs) were selected as instrumental variables. The IVW analysis reported that genetically predicted psoriasis was associated with a higher risk of CKD (OR: 1.025, 95%CI: 1.001-1.049). After removing 2 SNPs associated with heterogeneity, the association remained (OR: 1.028, 95%CI: 1.006-1.050).
Genetically predicted psoriasis was associated with a higher risk of CKD. This association may be important for clinicians to monitor kidney function and prescribe potentially nephrotoxic drugs during psoriasis management.</description><subject>Cross-sectional studies</subject><subject>Genomes</subject><subject>Kidney diseases</subject><subject>Population studies</subject><subject>Population-based studies</subject><subject>Psoriasis</subject><subject>Single-nucleotide polymorphism</subject><issn>1320-5358</issn><issn>1440-1797</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkU1v1DAQhq0KRD_g0D-ALHGhh5Rx7MTe3qoKWqQiOMA5mtgT4TYbp57NYRE_Hu_248BcPB_PvLb1CnGq4FyV-DTRfK5MXcOBOFLGQKXsyr4qua6hanTjDsUx8x2AsnWr3ohDbU27qpU5En9_cMoRObLEKcgc-V6mQfrfOU3Ry_sYJtrKEJmQiS_kpZzTvIy4iWmq-tIL0ufEXDH5XQ9HyZslbPdq32gKNEacZC5lWsc_-70yw3FbrnwrXg84Mr17Ok_Ery-ff17dVLffr79eXd5WXhu3qVoNXgM4o4JvWuvQrHoNmkzJAQIa51r0aHpNA1LTQK8I7WCcwRYQjT4RHx9155weFuJNt47saRxxorRwVzsDtbHK7tAP_6F3acnlvTvKggPXalWos0dq__dMQzfnuMa87RR0O0u6Ykm3t6Sw758Ul35N4YV89kD_A-JGh9c</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Yin, Saifu</creator><creator>Zhou, Zhaoxia</creator><creator>Wu, Jiapei</creator><creator>Wang, Xianding</creator><creator>Lin, Tao</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9710-7872</orcidid></search><sort><creationdate>20231101</creationdate><title>Psoriasis and risk of chronic kidney diseases: A population-based cross-sectional study and Mendelian randomization analysis</title><author>Yin, Saifu ; Zhou, Zhaoxia ; Wu, Jiapei ; Wang, Xianding ; Lin, Tao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-630c300841dc5678a49b303e467800da4886aca4b3efae550b1ea7f484a60aa43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cross-sectional studies</topic><topic>Genomes</topic><topic>Kidney diseases</topic><topic>Population studies</topic><topic>Population-based studies</topic><topic>Psoriasis</topic><topic>Single-nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yin, Saifu</creatorcontrib><creatorcontrib>Zhou, Zhaoxia</creatorcontrib><creatorcontrib>Wu, Jiapei</creatorcontrib><creatorcontrib>Wang, Xianding</creatorcontrib><creatorcontrib>Lin, Tao</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Nephrology (Carlton, Vic.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yin, Saifu</au><au>Zhou, Zhaoxia</au><au>Wu, Jiapei</au><au>Wang, Xianding</au><au>Lin, Tao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Psoriasis and risk of chronic kidney diseases: A population-based cross-sectional study and Mendelian randomization analysis</atitle><jtitle>Nephrology (Carlton, Vic.)</jtitle><addtitle>Nephrology (Carlton)</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>28</volume><issue>11</issue><spage>611</spage><epage>619</epage><pages>611-619</pages><issn>1320-5358</issn><eissn>1440-1797</eissn><abstract>Conflicting results have been reported regarding the association between psoriasis and risk of chronic kidney diseases (CKD). Furthermore, the causal nature of the possible association remains unexplored.
We conducted a population-based cross-sectional study using data from National Health and Nutrition Examination Survey (NHANES). Logistic regression analyses were conducted to estimate potential association between psoriasis and CKD risk. Further, we evaluated causality by performing a Mendelian randomization analysis using large-scale genome-wide association studies of psoriasis and CKD. Inverse variance-weighted (IVW) analysis was used as the primary method.
In the observational study, 16 750 participants were included. Overall, 39 of 429 patients with psoriasis had CKD (9.1%) compared with 1481 of 16 321 without psoriasis (9.1%). In the fully adjusted model, psoriasis was not associated with CKD (OR: 0.77, 95%CI: 0.53-1.10). In the MR analysis, 36 single-nucleotide polymorphisms (SNPs) were selected as instrumental variables. The IVW analysis reported that genetically predicted psoriasis was associated with a higher risk of CKD (OR: 1.025, 95%CI: 1.001-1.049). After removing 2 SNPs associated with heterogeneity, the association remained (OR: 1.028, 95%CI: 1.006-1.050).
Genetically predicted psoriasis was associated with a higher risk of CKD. This association may be important for clinicians to monitor kidney function and prescribe potentially nephrotoxic drugs during psoriasis management.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37469214</pmid><doi>10.1111/nep.14220</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-9710-7872</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cross-sectional studies Genomes Kidney diseases Population studies Population-based studies Psoriasis Single-nucleotide polymorphism |
title | Psoriasis and risk of chronic kidney diseases: A population-based cross-sectional study and Mendelian randomization analysis |
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