Johann Steiner, Henrik Dobrowolny, Paul C Guest, Hans-Gert Bernstein, Dietmar Fuchs, Julien Roeser, Paul Summergrad, Gregory F Oxenkrug
{"title":"血浆邻氨基苯酸和瘦素水平预测抑郁女性的HAM-D评分。","authors":"Johann Steiner, Henrik Dobrowolny, Paul C Guest, Hans-Gert Bernstein, Dietmar Fuchs, Julien Roeser, Paul Summergrad, Gregory F Oxenkrug","doi":"10.1177/11786469211016474","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Major depressive disorder (MDD) is associated with dysregulations of leptin and tryptophan-kynurenine (Trp-Kyn) (TKP) pathways. Leptin, a pro-inflammatory cytokine, activates Trp conversion into Kyn. However, leptin association with down-stream Kyn metabolites in MDD is unknown.</p><p><strong>Methods: </strong>Fasting plasma samples from 29 acutely ill drug-naïve (n = 16) or currently non-medicated (⩾6 weeks; n = 13) MDD patients were analyzed for leptin, Trp, Kyn, its down-stream metabolites (anthranilic [AA], kynurenic [KYNA], xanthurenic [XA] acids and 3-hydroxykynurenine [3HK]), C-reactive protein (CRP), neopterin, body mass index (BMI), and insulin resistance (HOMA-IR). Depression severity was assessed by HAM-D-21.</p><p><strong>Results: </strong>In female (n = 14) (but not in male) patients HAM-D-21 scores correlated with plasma levels of AA (but not other Kyn metabolites) (rho = -0.644, <i>P</i> = .009) and leptin (Spearman's rho = -0.775, <i>P</i> = .001). Inclusion of AA into regression analysis improved leptin prediction of HAM-D from 48.5% to 65.9%. Actual HAM-D scores highly correlated with that calculated by formula: HAM-D = 34.8518-(0.5660 × leptin [ng/ml] + 0.4159 × AA [nmol/l]) (Rho = 0.84, <i>P</i> = .00015). In male (n = 15) (but not in female) patients leptin correlated with BMI, waist circumference/hip ratio, CRP, and HOMA-IR.</p><p><strong>Conclusions: </strong>Present findings of gender specific AA/Leptin correlations with HAM-D are important considering that AA and leptin are transported from plasma into brain, and that AA formation is catalyzed by <i>kynureninase</i>-the only TKP gene associated with depression according to genome-wide analysis. High correlation between predicted and actual HAM-D warrants further evaluation of plasma AA and leptin as an objective laboratory test for the assessment of depression severity in female MDD patients.</p>","PeriodicalId":46603,"journal":{"name":"International Journal of Tryptophan Research","volume":"14 ","pages":"11786469211016474"},"PeriodicalIF":2.7000,"publicationDate":"2021-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/11786469211016474","citationCount":"7","resultStr":"{\"title\":\"Plasma Anthranilic Acid and Leptin Levels Predict HAM-D Scores in Depressed Women.\",\"authors\":\"Johann Steiner, Henrik Dobrowolny, Paul C Guest, Hans-Gert Bernstein, Dietmar Fuchs, Julien Roeser, Paul Summergrad, Gregory F Oxenkrug\",\"doi\":\"10.1177/11786469211016474\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>Major depressive disorder (MDD) is associated with dysregulations of leptin and tryptophan-kynurenine (Trp-Kyn) (TKP) pathways. Leptin, a pro-inflammatory cytokine, activates Trp conversion into Kyn. However, leptin association with down-stream Kyn metabolites in MDD is unknown.</p><p><strong>Methods: </strong>Fasting plasma samples from 29 acutely ill drug-naïve (n = 16) or currently non-medicated (⩾6 weeks; n = 13) MDD patients were analyzed for leptin, Trp, Kyn, its down-stream metabolites (anthranilic [AA], kynurenic [KYNA], xanthurenic [XA] acids and 3-hydroxykynurenine [3HK]), C-reactive protein (CRP), neopterin, body mass index (BMI), and insulin resistance (HOMA-IR). Depression severity was assessed by HAM-D-21.</p><p><strong>Results: </strong>In female (n = 14) (but not in male) patients HAM-D-21 scores correlated with plasma levels of AA (but not other Kyn metabolites) (rho = -0.644, <i>P</i> = .009) and leptin (Spearman's rho = -0.775, <i>P</i> = .001). Inclusion of AA into regression analysis improved leptin prediction of HAM-D from 48.5% to 65.9%. Actual HAM-D scores highly correlated with that calculated by formula: HAM-D = 34.8518-(0.5660 × leptin [ng/ml] + 0.4159 × AA [nmol/l]) (Rho = 0.84, <i>P</i> = .00015). In male (n = 15) (but not in female) patients leptin correlated with BMI, waist circumference/hip ratio, CRP, and HOMA-IR.</p><p><strong>Conclusions: </strong>Present findings of gender specific AA/Leptin correlations with HAM-D are important considering that AA and leptin are transported from plasma into brain, and that AA formation is catalyzed by <i>kynureninase</i>-the only TKP gene associated with depression according to genome-wide analysis. 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引用次数: 7
摘要
目的:重度抑郁症(MDD)与瘦素和色氨酸-犬尿氨酸(Trp-Kyn) (TKP)通路的失调有关。瘦素,一种促炎细胞因子,激活色氨酸转化为Kyn。然而,瘦素与MDD中下游Kyn代谢物的关联尚不清楚。方法:来自29名急性疾病drug-naïve (n = 16)或目前未服药的空腹血浆样本(小于或等于6周;n = 13)分析MDD患者的瘦素、色氨酸、Kyn及其下游代谢物(anthranilic [AA]、犬尿酸[KYNA]、黄尿酸[XA]酸和3-羟基犬尿酸[3HK])、c -反应蛋白(CRP)、新蝶呤、体重指数(BMI)和胰岛素抵抗(HOMA-IR)。采用HAM-D-21量表评估抑郁严重程度。结果:在女性(n = 14)(而非男性)患者中,HAM-D-21评分与血浆AA(但与其他Kyn代谢物无关)(rho = -0.644, P = 0.009)和瘦素(Spearman's rho = -0.775, P = 0.001)水平相关。将AA纳入回归分析将瘦素预测从48.5%提高到65.9%。HAM-D = 34.8518-(0.5660 ×瘦素[ng/ml] + 0.4159 × AA [nmol/l]) (Rho = 0.84, P = 0.00015)与实际HAM-D评分高度相关。在男性(n = 15)患者中,瘦素与BMI、腰围/臀围比、CRP和HOMA-IR相关。结论:考虑到AA和瘦素从血浆转运到大脑,并且AA的形成是由犬尿氨酸酶(kynureninase)催化的——根据全基因组分析,这是唯一与抑郁症相关的TKP基因,目前的性别特异性AA/Leptin与HAM-D的相关性研究结果是重要的。预测的HAM-D与实际的HAM-D高度相关,值得进一步评估血浆AA和瘦素作为评估女性MDD患者抑郁严重程度的客观实验室检测。
Plasma Anthranilic Acid and Leptin Levels Predict HAM-D Scores in Depressed Women.
Objectives: Major depressive disorder (MDD) is associated with dysregulations of leptin and tryptophan-kynurenine (Trp-Kyn) (TKP) pathways. Leptin, a pro-inflammatory cytokine, activates Trp conversion into Kyn. However, leptin association with down-stream Kyn metabolites in MDD is unknown.
Methods: Fasting plasma samples from 29 acutely ill drug-naïve (n = 16) or currently non-medicated (⩾6 weeks; n = 13) MDD patients were analyzed for leptin, Trp, Kyn, its down-stream metabolites (anthranilic [AA], kynurenic [KYNA], xanthurenic [XA] acids and 3-hydroxykynurenine [3HK]), C-reactive protein (CRP), neopterin, body mass index (BMI), and insulin resistance (HOMA-IR). Depression severity was assessed by HAM-D-21.
Results: In female (n = 14) (but not in male) patients HAM-D-21 scores correlated with plasma levels of AA (but not other Kyn metabolites) (rho = -0.644, P = .009) and leptin (Spearman's rho = -0.775, P = .001). Inclusion of AA into regression analysis improved leptin prediction of HAM-D from 48.5% to 65.9%. Actual HAM-D scores highly correlated with that calculated by formula: HAM-D = 34.8518-(0.5660 × leptin [ng/ml] + 0.4159 × AA [nmol/l]) (Rho = 0.84, P = .00015). In male (n = 15) (but not in female) patients leptin correlated with BMI, waist circumference/hip ratio, CRP, and HOMA-IR.
Conclusions: Present findings of gender specific AA/Leptin correlations with HAM-D are important considering that AA and leptin are transported from plasma into brain, and that AA formation is catalyzed by kynureninase-the only TKP gene associated with depression according to genome-wide analysis. High correlation between predicted and actual HAM-D warrants further evaluation of plasma AA and leptin as an objective laboratory test for the assessment of depression severity in female MDD patients.