Academic literature on the topic 'Skin, diseases, psychosomatic aspects'
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Journal articles on the topic "Skin, diseases, psychosomatic aspects"
Varzhapetyan, Asmik A., I. Yu Dorozhenok, and K. M. Lomonosov. "VITILIGO AND COMORBID PSYCHOSOMATIC DISORDERS." Russian Journal of Skin and Venereal Diseases 22, no. 1-2 (April 15, 2019): 33–38. http://dx.doi.org/10.17816/dv42934.
Full textDa Silva, Lucielma Maria. "Alopecia and Emotional Aspects Related to Hair." Brazilian Journal of Hair Health 1, no. 1 (May 8, 2024): bjhh11. http://dx.doi.org/10.62742/2965-7911.2024.1.bjhh11.
Full textHarth, Wolfgang, and Ulrike Blume-Peytavi. "Psychotrichology: psychosomatic aspects of hair diseases." JDDG: Journal der Deutschen Dermatologischen Gesellschaft 11, no. 2 (November 26, 2012): 125–35. http://dx.doi.org/10.1111/j.1610-0387.2012.08034.x.
Full textBelugina, Olga. "Psychosomatic aspects of psoriasis and atopic dermatitis." BJPsych Open 7, S1 (June 2021): S7—S8. http://dx.doi.org/10.1192/bjo.2021.80.
Full textPicardi, Angelo, Paolo Pasquini, Damiano Abeni, Giovanni Fassone, Eva Mazzotti, and Giovanni A. Fava. "Psychosomatic Assessment of Skin Diseases in Clinical Practice." Psychotherapy and Psychosomatics 74, no. 5 (2005): 315–22. http://dx.doi.org/10.1159/000086323.
Full textDorozhenok, I. Yu. "Nosogenic psychosomatic disorders in patients with skin diseases." Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 123, no. 4 (2023): 36. http://dx.doi.org/10.17116/jnevro202312304236.
Full textMoser, Gabriele. "Psychosomatik der Darmerkrankungen/ Psychosomatic aspects of bowel diseases." Zeitschrift für Psychosomatische Medizin und Psychotherapie 52, no. 2 (July 2006): 112–26. http://dx.doi.org/10.13109/zptm.2006.52.2.112.
Full textDorozhenok, I. Yu, E. S. Snarskaya, and М. Mikhailova. "Psychosomatic disorders associated with pruritus in patients with lichen planus (review)." Russian Journal of Skin and Venereal Diseases 23, no. 1 (August 2, 2020): 42–49. http://dx.doi.org/10.17816/dv2020142-49.
Full textShafaei, Hassan, Elena G. Ichitovkina, and Sergey V. Zhernov. "Psychosocial aspects for effectiveness of complex rehabilitation treatment among patients with psychosomatic diseases." Psychological-Pedagogical Journal GAUDEAMUS, no. 1 (2023): 55–66. http://dx.doi.org/10.20310/1810-231x-2023-22-1-55-66.
Full textDorozhenok, Igor Yu, and Ekaterina V. Ilina. "Psychosomatic aspects of psoriasis (review)." Russian Journal of Skin and Venereal Diseases 24, no. 3 (June 15, 2021): 251–62. http://dx.doi.org/10.17816/dv71927.
Full textDissertations / Theses on the topic "Skin, diseases, psychosomatic aspects"
Lonne-Rahm, Sol-Britt. "Etiological and clinical aspects of skin sensitivity /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-746-0.
Full textBroderick, Daniel J. "Mitral valve prolapse syndrome : a proposed treatment through respiratory rebalancing." Virtual Press, 1996. http://liblink.bsu.edu/uhtbin/catkey/1027110.
Full textDepartment of Counseling Psychology and Guidance Services
Lai, Josanna Yuk-Lin. "Is keeping in or letting out anger good for your heart?" Thesis, University of British Columbia, 1990. http://hdl.handle.net/2429/30099.
Full textArts, Faculty of
Psychology, Department of
Graduate
Meyer, Joana Ladeira [UNESP]. "Avaliação do padrão de metilação de regiões promotoras dos genes ESR1, ESR2 e PGR na endometriose profunda intestinal." Universidade Estadual Paulista (UNESP), 2011. http://hdl.handle.net/11449/92428.
Full textCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
A endometriose é uma doença inflamatória estrógeno-dependente que afeta de 5 a 10% das mulheres em idade reprodutiva. É caracterizada pela presença de tecido endometrial fora da cavidade uterina e está associada à dismenorreia, dor pélvica e infertilidade. Os níveis de expressão dos receptores nucleares SF1 (fator esteroidogênico 1), estrógeno e progesterona estão alterados no tecido endometriótico comparado ao endométrio normal. Estudos prévios relataram que os genes codificadores dos receptores dos hormônios esteróides ESR1 (receptor de estrógeno 1), ESR2 (receptor de estrógeno 2) e progesterona (PGR) apresentam promotores alternativos que são modulados epigeneticamente por alterações na metilação do DNA, que ocorre preferencialmente nas ilhas CpG presentes nestas regiões. Em células endometriais normais foi observada uma associação entre a presença de metilação e ausência de expressão dos genes SF1 e ESR2 (receptor de estrógeno â) enquanto a perda da metilação foi correlacionada com níveis aumentados de expressão gênica na endometriose peritoneal e ovariana. Com base nestas evidências, o presente trabalho investigou o padrão de metilação dos genes PGR (promotores A e B), ESR1 (promotores A e B) e uma região intragênica ao ESR2. O promotor B do gene PGR e a ilha CpG localizada na 5’UTR do gene ESR2 foram avaliadas em 44 amostras de endometriose profunda intestinal pela técnica de MSP (Methylation-Specific Polymerase Chain Reaction). Em sete destas, também foi possível a investigação na amostra pareada de endométrio eutópico. O padrão de metilação dos promotores A e B do gene ESR1 e o promotor A do gene PGR...
Endometriosis is an estrogen-dependent inflammatory disease which affects 5 to 10% of women of reproductive age. This disease is characterized by the presence of endometrial tissue outside the uterine cavity and is associated with dysmenorrhea, pelvic pain, and infertility. Abnormal expression levels of SF1 (steroidogenic factor 1), estrogen and progesterone nuclear receptors were detected in the endometriotic tissue compared to the normal endometrium. Previous studies have reported that genes encoding the steroid hormone receptors ESR1 (estrogen receptor 1), ESR2 (estrogen receptor 2) and progesterone (PGR) are characterized by alternative promoters epigenetically regulated by DNA methylation at CpG islands co-localized in these regions. In normal endometrial cells, it was observed an association between DNA methylation and absence of expression of the genes SF1 and ESR2 (estrogen receptor â), while loss of DNA methylation was correlated with increased expression levels of these genes in peritoneal and ovarian endometriosis. Based on these findings, this study investigated the methylation pattern of the PGR (promoters A and B), ESR1 (promoters A and B) genes and an intragenic region of the gene ESR2. The promoter B of PGR gene and the CpG island mapped at 5 'UTR of the ESR2 gene were evaluated in 44 samples of intestinal deep endometriosis by MSP (methylation-specific polymerase chain reaction). In seven cases, paired samples of eutopic endometrium from the same patients were also evaluated, the methylation patterns of the ESR1 gene (promoters A and B) and the promoter region A of the PGR gene were investigated in 37 samples of endometriosis. The MSP method is based on the DNA modification by sodium bisulfite, which converts unmethylated cytosines to uracil. Subsequently, the target region... (Complete abstract click electronic access below)
Burgess, Carolyn E. "Sexual Function in Women Following Treatment for Cervical Dysplasia and Microinvasive Cervical Carcinoma." Thesis, North Texas State University, 1985. https://digital.library.unt.edu/ark:/67531/metadc331592/.
Full textMeyer, Joana Ladeira. "Avaliação do padrão de metilação de regiões promotoras dos genes ESR1, ESR2 e PGR na endometriose profunda intestinal /." Botucatu : [s.n.], 2011. http://hdl.handle.net/11449/92428.
Full textBanca: Roberta Guembarovisk
Banca: Celia Regina Nogueira
Resumo: A endometriose é uma doença inflamatória estrógeno-dependente que afeta de 5 a 10% das mulheres em idade reprodutiva. É caracterizada pela presença de tecido endometrial fora da cavidade uterina e está associada à dismenorreia, dor pélvica e infertilidade. Os níveis de expressão dos receptores nucleares SF1 (fator esteroidogênico 1), estrógeno e progesterona estão alterados no tecido endometriótico comparado ao endométrio normal. Estudos prévios relataram que os genes codificadores dos receptores dos hormônios esteróides ESR1 (receptor de estrógeno 1), ESR2 (receptor de estrógeno 2) e progesterona (PGR) apresentam promotores alternativos que são modulados epigeneticamente por alterações na metilação do DNA, que ocorre preferencialmente nas ilhas CpG presentes nestas regiões. Em células endometriais normais foi observada uma associação entre a presença de metilação e ausência de expressão dos genes SF1 e ESR2 (receptor de estrógeno â) enquanto a perda da metilação foi correlacionada com níveis aumentados de expressão gênica na endometriose peritoneal e ovariana. Com base nestas evidências, o presente trabalho investigou o padrão de metilação dos genes PGR (promotores A e B), ESR1 (promotores A e B) e uma região intragênica ao ESR2. O promotor B do gene PGR e a ilha CpG localizada na 5'UTR do gene ESR2 foram avaliadas em 44 amostras de endometriose profunda intestinal pela técnica de MSP (Methylation-Specific Polymerase Chain Reaction). Em sete destas, também foi possível a investigação na amostra pareada de endométrio eutópico. O padrão de metilação dos promotores A e B do gene ESR1 e o promotor A do gene PGR... (Resumo completo, clicar acesso eletrônico abaixo)
Abstract: Endometriosis is an estrogen-dependent inflammatory disease which affects 5 to 10% of women of reproductive age. This disease is characterized by the presence of endometrial tissue outside the uterine cavity and is associated with dysmenorrhea, pelvic pain, and infertility. Abnormal expression levels of SF1 (steroidogenic factor 1), estrogen and progesterone nuclear receptors were detected in the endometriotic tissue compared to the normal endometrium. Previous studies have reported that genes encoding the steroid hormone receptors ESR1 (estrogen receptor 1), ESR2 (estrogen receptor 2) and progesterone (PGR) are characterized by alternative promoters epigenetically regulated by DNA methylation at CpG islands co-localized in these regions. In normal endometrial cells, it was observed an association between DNA methylation and absence of expression of the genes SF1 and ESR2 (estrogen receptor â), while loss of DNA methylation was correlated with increased expression levels of these genes in peritoneal and ovarian endometriosis. Based on these findings, this study investigated the methylation pattern of the PGR (promoters A and B), ESR1 (promoters A and B) genes and an intragenic region of the gene ESR2. The promoter B of PGR gene and the CpG island mapped at 5 'UTR of the ESR2 gene were evaluated in 44 samples of intestinal deep endometriosis by MSP (methylation-specific polymerase chain reaction). In seven cases, paired samples of eutopic endometrium from the same patients were also evaluated, the methylation patterns of the ESR1 gene (promoters A and B) and the promoter region A of the PGR gene were investigated in 37 samples of endometriosis. The MSP method is based on the DNA modification by sodium bisulfite, which converts unmethylated cytosines to uracil. Subsequently, the target region... (Complete abstract click electronic access below)
Mestre
Eyjolfsdottir, Gyda 1970. "Psychosocial aspects and functional analysis of symptom-giving pelvic girdle relaxation in Icelandic women." 2004. http://hdl.handle.net/2152/12710.
Full text"The roles of CCHCR1 protein in skin epidermal cell proliferation." 2009. http://library.cuhk.edu.hk/record=b59646408.b5964640.
Full text方法:本研究應用免疫螢光技術'免疫印跡分析和即時反轉錄聚合臨鏈反應 (Real Time RT-PCR) 三種方法比較CCHCRl 基因在銀屑病人的皮損區與正常人的皮膚細胞的表達。其次比較了CCHCRl 蛋白在喜樹鹼(拓撲異構酪I 抑制劑/凋亡誘導劑)的作用下在三種細胞(永生化的人皮膚角質形成細胞-HaCaT '人直結腸癌細胞-HT29 和人子宮頸癌細胞- HeLa) 內的表達。最後,我們應用了皮膚器官樣培養物( OTC) 研究HaCaT 細胞於皮膚角質化過程中CCHCRl 蛋白的表達。
結果:✹HCR1 蛋白在正常皮膚和銀屑病人皮損皮膚表達模式不同,銀屑病人皮損皮膚有五種CCHCR1 蛋白染色模式,而正常人皮膚只有兩種染色模式。免疫印跡分析顯示CCHCR1 蛋白在正常皮膚含量較銀屑病人高。免役螢光顯微技術顯示角蛋白17 (K17) ,一種細胞增生的標誌性蛋白,只表達在正常皮膚基底層的角質細胞中,而在銀屑病人皮膚, K17 從基底層到顆粒層都有顯著表達,並且和CCHCR1 蛋白表達區域相同。這種現象也存在於OTC 發育過程中所有角質細胞中,而CCHCR1 蛋白表達隨OTC 的培養時間從10 天到21 天呈上升趨勢,說明CCHCR1 蛋白與細胞增殖有一定的關係。當細胞生長在培養血表面形成細胞與細胞接合全面的細胞層時, CCHCR1 的信使核糖核酸水平大幅升高,顯示CCHCR1 的信使核糖核酸表達當細胞生長速度呈負相關。CCHCR1 的信使核糖核酸水平在同步化的HaCaT 細胞G2/M 期輕度升高,而蛋白水平在G1 期達到最高。在G2/M 期,高爾基體出現崩解,而CCHCR1 蛋白和其他高爾基蛋白一樣分散到胞漿。這種現象同樣地出現在經2 州喜樹鹼刺激48小時的HeLa 和HaCaT 細胞內,免疫細胞化學染色顯示CCHCR1 和golgin-97 分散到胞漿。CCHCR1 信使核糖核酸水平在HeLa 和HaCaT 細胞都升高,而蛋白在HaCaT 細胞明顯上調。這說明CCHCR1 蛋白量的上調和細胞生長停滯有關。應用siRNA 或shRNA 抑制CCHCR1 蛋白表達後, golgin-97 分散到胞漿,但是HeLa細胞可以繼續增殖。這說明CCHCR1 蛋白可能有助於維持高爾基複合體的完整,喜樹鹼對細胞生長的抑制作用可能與CCHCR1 蛋白的上調相關。
結論: CCHCR1 蛋白在正常皮膚表皮細胞和銀屑病人皮損區細胞胞漿內都有表達,但是正常皮膚表達較銀屑病人高,在OTC 增生後期和細胞生長緩慢或停滯期也明顯升高,說明CCHCRl 基因的上調可能抑制細胞的增生。經喜樹鹼刺激後,細胞生長受到抑制,細胞停滯在Gl 期並誘導細胞凋亡, CCHCRl 的信使核糖核酸和蛋白都上調,表明CCHCRl 與細胞的增生抑制有關。同時,它的下調也造成高爾基複合體的崩解,說明CCHCRl 蛋白可以維持高爾基複合體的結構完整性。因此, CCHCRl 不僅可以保持高爾基複合體的完整而且和細胞的增生有關。另一方面,大量證據表明長期性的高血糖會導致胰島 細胞功能紊亂。鑒於此,揭示胰島功能調節的潛在機理并闡明胰島功能与高血糖症之間的關係變得尤為重要。
Aim: Psoriasis is one of the common chronic inflammatory skin disorders characterized by keratinocyte hyperproliferation, T lymphocyte-mediated inflammation, and abnormal differentiation. Genome-wide scans have revealed that at least ten different susceptibility loci, PSORS1-PSORS10, were linked to psoriasis, among which PSORS 1 on chromosome 6p21.3 was unambiguously associated with families with psoriasis. Three strongly psoriasis-associated susceptibility alleles have been identified in PSORS1, namely HLA-C, CCHCR1 (coiled-coil alpha-helical rod protein 1 ), and CDSN ( comeodesmosin); their strong linkage disequilibrium, however, makes it very difficult to distinguish their individual genetic effects. Among them, we were interested in the CCHCR1 gene, and its possible roles with associated proteins in the process of skin epidermal cell proliferation were studied in this thesis.
Methods: The cellular expressiOn of CCHCR1 protein in the epidermis was compared between human skins from healthy donors and psoriasis patients by immunofluorescence microscopy and immunoblotting analysis. Its intracellular expression was investigated in cultured human immortalized skin keratinocyte cell line (HaCaT), human colorectal cancer cell line (HT29) and human cervical carcinoma HeLa cell line, as well as in the skin keratinocyte-fibroblast organotypic culture (OTC). The responses of these cells to camptothecin (CPT), a topoisomerase I inhibitor, were compared in HaCaT cells, HT29 cells and HeLa cells. In cell experiments, CCHCR1 expression was studied by immunofluorescence microscopy, immunoblotting analysis, and real-time reverse transcriptase-polymerase chain reaction (real-time RT-PCR).
Results: The immunofluorescence staining patterns for CCHCR1 protein were different between normal and psoriasis skin biopsies. There were at least five patterns (Patterns I, III-VI) in psoriatic skins, but only two (Patterns I and II) in the normal skin, implicating that the expression of CCHCR1 protein was changed in psoriasis. Besides the different cellular location of CCHCR1 protein in normal and psoriasis skins, a higher level of CCHCR1 expression was measured in normal skin than that in psoriatic skin by immunoblotting analysis, and immunofluorescence microscopy further revealed a co-localization of CCHCR1 protein with keratin 17 (K17), a proliferation marker protein and also putative autoantigen for psoriasis, to basal keratinocytes of normal skins, and extended further fro m the basal to granular keratinocytes in the epidermis of psoriasis patients, suggesting a close association of CCHCR1 protein to cell proliferation. During epidermal development in OTC, the CCHCR1 protein was expressed in all keratinocyte layers in a time-dependent manner from day 1 0 to day 21, reaching a maximal level at day 21 when cell proliferation decreased and differentiation to the corneum became active. Furthermore, immunofluorescence for K17 remained co-localized to CCHCR1-positive cells in OTC from day 10 to day 14, but the level of K17 was very weak in the keratinocytes of suprabasallayers on day 21. In HaCaT cell culture, CCHCR1 transcription level at 100% confluence was 25 folds higher than that in subconfluence. Taken all these results together, the up-regulation of CCHCR1 was closely related to cell growth inhibition and differentiation. Immunofluorescence microscopy revealed a co-localization of CCHCR1 protein with a Golgi marker protein, golgin-97, in the compact Golgi complex at the juxtanuclear region of HaCaT cells and HeLa cells. CCHCR1 gene transcribed in all phases of the cell cycle, but was slightly higher in the G2/M phase of synchronous HaCaT cells, and its translation reached its maximal level in the G 1 phase. In the G2/M phase, CCHCR1 protein was dispersed in the cytoplasm like the golgin. Such dispersal was also observed in HaCaT cells and HeLa cells treated with CPT for 24 h and 48 h, respectively. CCHCR1 expression increased in both transcriptional and translational levels as well as apoptotic changes following growth arrest in both HeLa cells and HaCaT cells. Depletion of the CCHCR1 protein by means of siRNAor shRNA-mediated knockdown induced HeLa cells proliferation, cell elongation and disassembly of the Golgi complex.
Conclusion: CCHCR1 protein was expressed in the cytoplasm of epidermal keratinocytes of both normal and psoriasis skins, with a higher level detected in the normal skins. It was also found especially abundant in the keratinocytes of skin organotypic cultures during their transition from proliferation to differentiation. CCHCR1 gene transcription was increased obviously in cultured HaCaT cells at confluence. CCHCR1 was also up-regulated at both transcriptional and translational levels in response to the antiproliferative drug, camptothecin, in HaCaT cell experiments, and was accompanied by G 1 arrest and subsequent apoptosis. When CCHCR1 was knockdowned in HeLa cells, the Golgi complex disassembled, implicating a role of CCHCRl protein in the maintenance of Golgi integrity and in the control of cell proliferation.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Detailed summary in vernacular field only.
Wang, Lijun.
Thesis (Ph.D.)--Chinese University of Hong Kong, 2009.
Includes bibliographical references (leaves 107-133).
Abstracts also in Chinese.
Abstract --- p.i
Acknowledgements --- p.viii
List of Abbreviation --- p.ix
Chapter Chapter 1 --- General Introduction --- p.1
Chapter 1.1 --- Psoriasis --- p.1
Chapter 1.2 --- Skin --- p.9
Chapter 1.3 --- An In Vitro Model for Human Skin Equivalent --- p.10
Chapter 1.4 --- Aim of Study --- p.12
Chapter Chapter2 --- Expression of CCHCRl Protein in Psoriasis skin --- p.13
Chapter 2.1 --- Background of Skin and Psoriasis --- p.13
Chapter 2.2 --- Materials and Methods --- p.18
Chapter 2.3 --- Results --- p.21
Chapter 2.4 --- Discussion and Conclusion --- p.25
Chapter Chapter3 --- Expression of CCHCRl Protein in Skin Organotypic Culture --- p.37
Chapter 3.1 --- Background about Skin Organotypic Culture --- p.37
Chapter 3.2 --- Materials and Methods --- p.41
Chapter 3.3 --- Results --- p.45
Chapter 3.4 --- Discussion and Conclusion --- p.49
Chapter Chapter4 --- Expression of CCHCRl Protein in HaCaT Cells Treated with Camptothecin --- p.60
Chapter 4.1 --- Background --- p.60
Chapter 4.2 --- Materials and Methods --- p.61
Chapter 4.3 --- Results --- p.68
Chapter 4.4 --- Discussion and Conclusion --- p.73
Chapter Chapter 5 --- General Discussion --- p.95
References --- p.107
Publications --- p.172
"Work-related stress and cardiovascular risk factors in Chinese." 2004. http://library.cuhk.edu.hk/record=b6073711.
Full text"April 2004."
Thesis (Ph.D.)--Chinese University of Hong Kong, 2004.
Includes bibliographical references (p. 159-175)
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Electronic reproduction. Ann Arbor, MI : ProQuest Information and Learning Company, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Mode of access: World Wide Web.
Abstracts in English and Chinese.
Berntson, Jessica. "Depressive Symptom Severity, Stressful Life Events, and Subclinical Atherosclerosis in African American Adults." Thesis, 2015. http://hdl.handle.net/1805/8476.
Full textProspective epidemiologic evidence indicates that both stressful life events (SLEs) and depression are associated with an increased risk of subclinical atherosclerosis and cardiovascular disease (CVD) events. Even though stressful life events (SLEs) and depression co-occur and may act together to influence cardiovascular disease (CVD) risk, these psychosocial factors have been mainly examined in isolation. For instance, depression may moderate the relationship between SLEs and CVD outcomes. I hypothesized that depressive symptoms would potentiate the deleterious effect of SLEs on subclinical atherosclerosis. This hypothesis is plausible, given that depressed adults exhibit exaggerated and prolonged sympathetic nervous system, hypothalamic-pituitary-adrenal (HPA) axis, and inflammatory responses to stress, which in turn could promote atherosclerosis. As compared to their nondepressed counterparts, depressed individuals may also be more likely to engage in maladaptive methods to cope with SLEs (e.g., increased tobacco use, alcohol use, and consumption of low-nutrient, energy dense foods), which could also promote atherosclerosis. I examined cross-sectional data from 274 to 279 (depending on the outcome measure) older, African American adults (mean age = 66 years, 67% female) with no evidence of clinical CVD or dementia who participated in the St. Louis African American Health-Heart study (2009–2011). Number of SLEs was assessed using the Life Events Calendar, a structured interview. From this interview, a continuous SLEs variable was computed (number of adult SLEs: 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11+). Severity of depression symptoms was measured using the 17-item Hamilton Rating Scale for Depression (HAM-D). Two measures of subclinical atherosclerosis were obtained: carotid intima-media thickness (CIMT; assessed by ultrasonography) and coronary artery calcification (CAC; assessed by multi-detector computerized tomography). I conducted linear (CIMT) and logistic (CAC) regression models, first adjusted for demographics (age, sex, education) and then fully-adjusted (demographics; mean arterial pressure; low density lipoprotein cholesterol (LDL-C), high density lipoprotein cholesterol (HDL-C); hemoglobin A1c; BMI; tobacco use; diabetes diagnosis; and use of antihypertensitve, lipid lowering, antidiabetic, and antidepressant medications). No main effects of SLEs or HAM-D were found for CIMT or CAC. There were also no SLEs by HAM-D interactions for CIMT or CAC. Because the current results are largely inconsistent with prior literature and there is a paucity of studies utilizing African American samples, future research is needed to examine the independent and interactive associations of SLEs and depressive symptoms with measures of subclinical atherosclerosis. If the present results are replicated, it may suggest that SLEs, depressive symptoms, and their interactive effect are not cardiotoxic among African American adults.
Books on the topic "Skin, diseases, psychosomatic aspects"
Grossbart, Ted A. Skin deep: A mind/body program for healthy skin. New York: W. Morrow, 1986.
Find full textGrossbart, Ted A. Skin deep: A mind/body program for healthy skin. Santa Fe, N.M: Health Press, 1992.
Find full textFrança, Katlein, and Mohammad Jafferany. Geriatric psychodermatology: Psychocutaneous disorders in the elderly. Hauppauge], New York: Nova Biomedical, 2015.
Find full textM, Koo John Y., and Lee Chai Sue, eds. Psychocutaneous medicine. New York: Marcel Dekker, 2003.
Find full textMaguire, Anne. Skin disease: A message from the soul : a treatise from a Jungian perspective of psychosomatic dermatology. London: Free Association Books, 2004.
Find full text1975-, Walker Carl, and Papadopoulos Linda, eds. Psychodermatology. Cambridge: Cambridge University Press, 2005.
Find full textAlain, Claudy, Euvrard Sylvie, and Kanitakis Jean, eds. Skin diseases after organ transplantation. Montrouge: Eurotext, 1998.
Find full textRey, Fernando Luis González. Personalidad, salud y modo de vida. Caracas: Fondo Editorial de Humanidades y Educación, Universidad Central de Venezuela, 1992.
Find full textD, Wuepper Kirk, Gedde-Dahl Tobias 1934-, and European Society for Dermatological Research Clinically Oriented International Symposium (1986 : Oslo, Norway), eds. Biology of heritable skin diseases. Basel: Karger, 1987.
Find full textE, Tur, ed. Environmental factors in skin diseases. Karger: Basel ; New York, 2007.
Find full textBook chapters on the topic "Skin, diseases, psychosomatic aspects"
Wolman, Benjamin B. "Skin Diseases." In Psychosomatic Disorders, 145–55. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5520-5_16.
Full textGupta, Madhulika A. "Aging Skin: Some Psychosomatic Aspects." In Textbook of Aging Skin, 959–69. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-89656-2_90.
Full textGupta, Madhulika A. "Aging Skin: Some Psychosomatic Aspects." In Textbook of Aging Skin, 1657–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-47398-6_90.
Full textGupta, Madhulika A. "Aging Skin: Some Psychosomatic Aspects." In Textbook of Aging Skin, 1–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27814-3_90-2.
Full textMcDougall, A. C. "Leprosy: Clinical Aspects." In Mycobacterial Skin Diseases, 119–36. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2227-3_5.
Full textTomecki, K. J. "Environmental (Atypical) Mycobacteria: Clinical Aspects." In Mycobacterial Skin Diseases, 105–17. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2227-3_4.
Full textHarahap, M. "Tuberculosis of the Skin: Clinical Aspects." In Mycobacterial Skin Diseases, 79–104. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2227-3_3.
Full textConvit, J., and M. I. Ulrich. "Leprosy: Bacterial, Pathological, Immunological and Immunopathological Aspects." In Mycobacterial Skin Diseases, 33–78. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2227-3_2.
Full textGrange, J. M. "Tuberculosis and Environmental (Atypical) Mycobacterioses: Bacterial Pathological and Immunological Aspects." In Mycobacterial Skin Diseases, 1–32. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-2227-3_1.
Full textGarg, Suruchi, Anuva Bansal, and Manjot Kaur Marwah. "Breast Augmentation: Cutaneous Aspects and Complications." In Skin Diseases in Females, 549–86. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-6065-8_26.
Full textConference papers on the topic "Skin, diseases, psychosomatic aspects"
Silva, CA, MJ Quartilho, JA Da Silva, A. Malcata, and A. Porto. "SAT0143 Psychosomatic aspects of fibromyalgia versus rheumatoid arthritis." In Annual European Congress of Rheumatology, Annals of the rheumatic diseases ARD July 2001. BMJ Publishing Group Ltd and European League Against Rheumatism, 2001. http://dx.doi.org/10.1136/annrheumdis-2001.602.
Full textSemak, A. N., E. G. Busko, and V. A. Stelmakh. "MEDICAL-ECOLOGICAL AND CYTOGENETIC ASSESSMENT OF INDICATORS OF THE SKIN OF DOMESTIC ANIMALS OF THE CANINE FAMILY (CANIDAE) AND FELIDS (FELIDAE) OF CENTRAL BELARUS." In SAKHAROV READINGS 2021: ENVIRONMENTAL PROBLEMS OF THE XXI CENTURY. International Sakharov Environmental Institute of Belarusian State University, 2021. http://dx.doi.org/10.46646/sakh-2021-2-107-110.
Full textLatorre Sánchez, Consuelo, Juan Antonio Solves, Joaquín Sanchiz Navarro, Ricardo Bayona Salvador, Jose Laparra, Nicolás Palomares, and Jose Solaz. "Methodology Based on 3D Thermal Scanner and AI Integration to Model Thermal Comfort and Ergonomics." In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001896.
Full textLiu, Yanyu, and Hong Chen. "Design of Children's Wearable Moxibustion Instrument Based on Emotional Design Theory." In 14th International Conference on Applied Human Factors and Ergonomics (AHFE 2023). AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1003474.
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