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Exploring disease interrelationships in patients with lymphatic disorders: A single center retrospective experience

Background The lymphatic contribution to the circulation is of paramount importance in regulating fluid homeostasis, immune cell trafficking/activation and lipid metabolism. In comparison to the blood vasculature, the impact of the lymphatics has been underappreciated, both in health and disease, li...

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Published in:Clinical and translational medicine 2022-04, Vol.12 (4), p.e760-n/a
Main Authors: Rockson, Stanley G., Zhou, Xin, Zhao, Lan, Hosseini, Davood K., Jiang, Xinguo, Sweatt, Andrew J., Kim, Dongeon, Tian, Wen, Snyder, Michael P., Nicolls, Mark R.
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Zhou, Xin
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Nicolls, Mark R.
description Background The lymphatic contribution to the circulation is of paramount importance in regulating fluid homeostasis, immune cell trafficking/activation and lipid metabolism. In comparison to the blood vasculature, the impact of the lymphatics has been underappreciated, both in health and disease, likely due to a less well‐delineated anatomy and function. Emerging data suggest that lymphatic dysfunction can be pivotal in the initiation and development of a variety of diseases across broad organ systems. Understanding the clinical associations between lymphatic dysfunction and non‐lymphatic morbidity provides valuable evidence for future investigations and may foster the discovery of novel biomarkers and therapies. Methods We retrospectively analysed the electronic medical records of 724 patients referred to the Stanford Center for Lymphatic and Venous Disorders. Patients with an established lymphatic diagnosis were assigned to groups of secondary lymphoedema, lipoedema or primary lymphovascular disease. Individuals found to have no lymphatic disorder were served as the non‐lymphatic controls. The prevalence of comorbid conditions was enumerated. Pairwise co‐occurrence pattern analyses, validated by Jaccard similarity tests, was utilised to investigate disease–disease interrelationships. Results Comorbidity analyses underscored the expected relationship between the presence of secondary lymphoedema and those diseases that damage the lymphatics. Cardiovascular conditions were common in all lymphatic subgroups. Additionally, statistically significant alteration of disease–disease interrelationships was noted in all three lymphatic categories when compared to the control population. Conclusions The presence or absence of a lymphatic disease significantly influences disease interrelationships in the study cohorts. As a physiologic substrate, the lymphatic circulation may be an underappreciated participant in disease pathogenesis. These relationships warrant further, prospective scrutiny and study. Patients from the Stanford Center for Lymphatic and Venous Disorders were clinically assessed for the presence/absence of lymphatic disorders. All relevant comorbid ICD‐10 diagnoses were tabulated to permit statistical analysis. The study disclosed that the presence of lymphatic dysfunction alters disease interrelationships. Future prospective study may provide novel concepts regarding disease pathogenesis and targeted molecular therapeutics.
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In comparison to the blood vasculature, the impact of the lymphatics has been underappreciated, both in health and disease, likely due to a less well‐delineated anatomy and function. Emerging data suggest that lymphatic dysfunction can be pivotal in the initiation and development of a variety of diseases across broad organ systems. Understanding the clinical associations between lymphatic dysfunction and non‐lymphatic morbidity provides valuable evidence for future investigations and may foster the discovery of novel biomarkers and therapies. Methods We retrospectively analysed the electronic medical records of 724 patients referred to the Stanford Center for Lymphatic and Venous Disorders. Patients with an established lymphatic diagnosis were assigned to groups of secondary lymphoedema, lipoedema or primary lymphovascular disease. Individuals found to have no lymphatic disorder were served as the non‐lymphatic controls. The prevalence of comorbid conditions was enumerated. Pairwise co‐occurrence pattern analyses, validated by Jaccard similarity tests, was utilised to investigate disease–disease interrelationships. Results Comorbidity analyses underscored the expected relationship between the presence of secondary lymphoedema and those diseases that damage the lymphatics. Cardiovascular conditions were common in all lymphatic subgroups. Additionally, statistically significant alteration of disease–disease interrelationships was noted in all three lymphatic categories when compared to the control population. Conclusions The presence or absence of a lymphatic disease significantly influences disease interrelationships in the study cohorts. As a physiologic substrate, the lymphatic circulation may be an underappreciated participant in disease pathogenesis. These relationships warrant further, prospective scrutiny and study. Patients from the Stanford Center for Lymphatic and Venous Disorders were clinically assessed for the presence/absence of lymphatic disorders. All relevant comorbid ICD‐10 diagnoses were tabulated to permit statistical analysis. The study disclosed that the presence of lymphatic dysfunction alters disease interrelationships. Future prospective study may provide novel concepts regarding disease pathogenesis and targeted molecular therapeutics.</description><identifier>ISSN: 2001-1326</identifier><identifier>EISSN: 2001-1326</identifier><identifier>DOI: 10.1002/ctm2.760</identifier><identifier>PMID: 35452183</identifier><language>eng</language><publisher>United States: John Wiley &amp; Sons, Inc</publisher><subject>Body mass index ; Cancer ; Clinical medicine ; Comorbidity ; co‐morbidity ; disease co‐occurrence ; disease interrelationship ; Generalized linear models ; Humans ; Hypotheses ; lipedema ; Lipedema - complications ; Lymphatic diseases ; Lymphatic Diseases - complications ; Lymphedema ; Lymphedema - complications ; Lymphedema - diagnosis ; Lymphedema - epidemiology ; lymphovascular disease ; Pathogenesis ; Patients ; Prospective Studies ; Radiation therapy ; Retrospective Studies</subject><ispartof>Clinical and translational medicine, 2022-04, Vol.12 (4), p.e760-n/a</ispartof><rights>2022 The Authors. published by John Wiley &amp; Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics</rights><rights>2022 The Authors. Clinical and Translational Medicine published by John Wiley &amp; Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4340-75959b1ab04189358cc784256e3092408d14eca815fd162b282a179d70cbfa6b3</citedby><cites>FETCH-LOGICAL-c4340-75959b1ab04189358cc784256e3092408d14eca815fd162b282a179d70cbfa6b3</cites><orcidid>0000-0003-1253-474X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2760827401/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2760827401?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35452183$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rockson, Stanley G.</creatorcontrib><creatorcontrib>Zhou, Xin</creatorcontrib><creatorcontrib>Zhao, Lan</creatorcontrib><creatorcontrib>Hosseini, Davood K.</creatorcontrib><creatorcontrib>Jiang, Xinguo</creatorcontrib><creatorcontrib>Sweatt, Andrew J.</creatorcontrib><creatorcontrib>Kim, Dongeon</creatorcontrib><creatorcontrib>Tian, Wen</creatorcontrib><creatorcontrib>Snyder, Michael P.</creatorcontrib><creatorcontrib>Nicolls, Mark R.</creatorcontrib><title>Exploring disease interrelationships in patients with lymphatic disorders: A single center retrospective experience</title><title>Clinical and translational medicine</title><addtitle>Clin Transl Med</addtitle><description>Background The lymphatic contribution to the circulation is of paramount importance in regulating fluid homeostasis, immune cell trafficking/activation and lipid metabolism. In comparison to the blood vasculature, the impact of the lymphatics has been underappreciated, both in health and disease, likely due to a less well‐delineated anatomy and function. Emerging data suggest that lymphatic dysfunction can be pivotal in the initiation and development of a variety of diseases across broad organ systems. Understanding the clinical associations between lymphatic dysfunction and non‐lymphatic morbidity provides valuable evidence for future investigations and may foster the discovery of novel biomarkers and therapies. Methods We retrospectively analysed the electronic medical records of 724 patients referred to the Stanford Center for Lymphatic and Venous Disorders. Patients with an established lymphatic diagnosis were assigned to groups of secondary lymphoedema, lipoedema or primary lymphovascular disease. Individuals found to have no lymphatic disorder were served as the non‐lymphatic controls. The prevalence of comorbid conditions was enumerated. Pairwise co‐occurrence pattern analyses, validated by Jaccard similarity tests, was utilised to investigate disease–disease interrelationships. Results Comorbidity analyses underscored the expected relationship between the presence of secondary lymphoedema and those diseases that damage the lymphatics. Cardiovascular conditions were common in all lymphatic subgroups. Additionally, statistically significant alteration of disease–disease interrelationships was noted in all three lymphatic categories when compared to the control population. Conclusions The presence or absence of a lymphatic disease significantly influences disease interrelationships in the study cohorts. As a physiologic substrate, the lymphatic circulation may be an underappreciated participant in disease pathogenesis. These relationships warrant further, prospective scrutiny and study. Patients from the Stanford Center for Lymphatic and Venous Disorders were clinically assessed for the presence/absence of lymphatic disorders. All relevant comorbid ICD‐10 diagnoses were tabulated to permit statistical analysis. The study disclosed that the presence of lymphatic dysfunction alters disease interrelationships. 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In comparison to the blood vasculature, the impact of the lymphatics has been underappreciated, both in health and disease, likely due to a less well‐delineated anatomy and function. Emerging data suggest that lymphatic dysfunction can be pivotal in the initiation and development of a variety of diseases across broad organ systems. Understanding the clinical associations between lymphatic dysfunction and non‐lymphatic morbidity provides valuable evidence for future investigations and may foster the discovery of novel biomarkers and therapies. Methods We retrospectively analysed the electronic medical records of 724 patients referred to the Stanford Center for Lymphatic and Venous Disorders. Patients with an established lymphatic diagnosis were assigned to groups of secondary lymphoedema, lipoedema or primary lymphovascular disease. Individuals found to have no lymphatic disorder were served as the non‐lymphatic controls. The prevalence of comorbid conditions was enumerated. Pairwise co‐occurrence pattern analyses, validated by Jaccard similarity tests, was utilised to investigate disease–disease interrelationships. Results Comorbidity analyses underscored the expected relationship between the presence of secondary lymphoedema and those diseases that damage the lymphatics. Cardiovascular conditions were common in all lymphatic subgroups. Additionally, statistically significant alteration of disease–disease interrelationships was noted in all three lymphatic categories when compared to the control population. Conclusions The presence or absence of a lymphatic disease significantly influences disease interrelationships in the study cohorts. As a physiologic substrate, the lymphatic circulation may be an underappreciated participant in disease pathogenesis. These relationships warrant further, prospective scrutiny and study. Patients from the Stanford Center for Lymphatic and Venous Disorders were clinically assessed for the presence/absence of lymphatic disorders. All relevant comorbid ICD‐10 diagnoses were tabulated to permit statistical analysis. The study disclosed that the presence of lymphatic dysfunction alters disease interrelationships. Future prospective study may provide novel concepts regarding disease pathogenesis and targeted molecular therapeutics.</abstract><cop>United States</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>35452183</pmid><doi>10.1002/ctm2.760</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-1253-474X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Body mass index
Cancer
Clinical medicine
Comorbidity
co‐morbidity
disease co‐occurrence
disease interrelationship
Generalized linear models
Humans
Hypotheses
lipedema
Lipedema - complications
Lymphatic diseases
Lymphatic Diseases - complications
Lymphedema
Lymphedema - complications
Lymphedema - diagnosis
Lymphedema - epidemiology
lymphovascular disease
Pathogenesis
Patients
Prospective Studies
Radiation therapy
Retrospective Studies
title Exploring disease interrelationships in patients with lymphatic disorders: A single center retrospective experience
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