<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wei Y</submitter><funding>The major project of the Eye Hospital of Wenzhou Medical University</funding><funding>The basic public welfare research project of Zhejiang province</funding><funding>The initial Scientific Research Fund</funding><pagination>e025336</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6830718</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(10)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>We investigated the association of specific serum amino acids (AAs) with the odds of arsenic-induced skin lesions (AISL) and their ability to distinguish patients with AISL from people chronically exposed to arsenic.&lt;h4>Design&lt;/h4>Case-control study.&lt;h4>Setting&lt;/h4>Three arsenic-exposed villages in Wuyuan County, Hetao Plain, Inner Mongolia, China were evaluated.&lt;h4>Participants&lt;/h4>Among the 450 residents aged 18-79 years, who were chronically exposed to arsenic via drinking water, 56 were diagnosed as having AISL (defined as cases). Another 56 participants without AISL, matched by gender and age (±1 year) from the same population, were examined as controls.&lt;h4>Main outcome measures and methods&lt;/h4>AA levels were determined by ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry-based metabolomics analysis. Potential confounding variables were identified via a standardised questionnaire and clinical examination. Multivariable conditional logistic regression model and receiver operating characteristic curve analyses were performed to investigate the relationship between specific AAs and AISL.&lt;h4>Results&lt;/h4>Tryptophan and phenylalanine levels were negatively associated with AISL (p&lt;0.05). Compared with that in the first quartile, the adjusted OR of AISL in the second, third and fourth quartiles were decreased by 44%, 88% and 79% for tryptophan and 30%, 80% and 80% for phenylalanine, respectively. The combination of these two higher-level AAs showed the lowest OR for AISL (OR=0.08; 95% CI 0.02 to 0.25; p&lt;0.001). Furthermore, both AAs showed a moderate ability to distinguish patients with AISL from the control, with the area under the curve (AUC; 95% CI) as 0.67 (0.57 to 0.77) for tryptophan and 0.70 (0.60 to 0.80) for phenylalanine (p&lt;0.05). The combined pattern with AUC (95% CI) was 0.72 (0.62 to 0.81), showing a sensitivity of 76.79% and specificity of 58.93% (p&lt;0.001).&lt;h4>Conclusions&lt;/h4>Specific AAs may be linked to AISL and play important roles in early AISL identification.&lt;h4>Trial registration number&lt;/h4>NCT02235948.</pubmed_abstract><journal>BMJ open</journal><pubmed_title>The association of tryptophan and phenylalanine are associated with arsenic-induced skin lesions in a Chinese population chronically exposed to arsenic via drinking water: a case-control study.</pubmed_title><pmcid>PMC6830718</pmcid><funding_grant_id>YNZD201602</funding_grant_id><funding_grant_id>LGF19H260011</funding_grant_id><funding_grant_id>KYQD170301</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zuo J</pubmed_authors><pubmed_authors>Jia C</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Mao G</pubmed_authors><pubmed_authors>Hou X</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors><pubmed_authors>Lan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>The association of tryptophan and phenylalanine are associated with arsenic-induced skin lesions in a Chinese population chronically exposed to arsenic via drinking water: a case-control study.</name><description>&lt;h4>Objectives&lt;/h4>We investigated the association of specific serum amino acids (AAs) with the odds of arsenic-induced skin lesions (AISL) and their ability to distinguish patients with AISL from people chronically exposed to arsenic.&lt;h4>Design&lt;/h4>Case-control study.&lt;h4>Setting&lt;/h4>Three arsenic-exposed villages in Wuyuan County, Hetao Plain, Inner Mongolia, China were evaluated.&lt;h4>Participants&lt;/h4>Among the 450 residents aged 18-79 years, who were chronically exposed to arsenic via drinking water, 56 were diagnosed as having AISL (defined as cases). Another 56 participants without AISL, matched by gender and age (±1 year) from the same population, were examined as controls.&lt;h4>Main outcome measures and methods&lt;/h4>AA levels were determined by ultra-high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry-based metabolomics analysis. Potential confounding variables were identified via a standardised questionnaire and clinical examination. Multivariable conditional logistic regression model and receiver operating characteristic curve analyses were performed to investigate the relationship between specific AAs and AISL.&lt;h4>Results&lt;/h4>Tryptophan and phenylalanine levels were negatively associated with AISL (p&lt;0.05). Compared with that in the first quartile, the adjusted OR of AISL in the second, third and fourth quartiles were decreased by 44%, 88% and 79% for tryptophan and 30%, 80% and 80% for phenylalanine, respectively. The combination of these two higher-level AAs showed the lowest OR for AISL (OR=0.08; 95% CI 0.02 to 0.25; p&lt;0.001). Furthermore, both AAs showed a moderate ability to distinguish patients with AISL from the control, with the area under the curve (AUC; 95% CI) as 0.67 (0.57 to 0.77) for tryptophan and 0.70 (0.60 to 0.80) for phenylalanine (p&lt;0.05). The combined pattern with AUC (95% CI) was 0.72 (0.62 to 0.81), showing a sensitivity of 76.79% and specificity of 58.93% (p&lt;0.001).&lt;h4>Conclusions&lt;/h4>Specific AAs may be linked to AISL and play important roles in early AISL identification.&lt;h4>Trial registration number&lt;/h4>NCT02235948.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2024-12-04T06:28:45.324Z</modification><creation>2020-05-21T19:04:36Z</creation></dates><accession>S-EPMC6830718</accession><cross_references><pubmed>31666259</pubmed><doi>10.1136/bmjopen-2018-025336</doi></cross_references></HashMap>