粪菌移植促进老年斑秃患者头发再生及相好转黑
2025-10-03 12:16:17
FMT 疗程后随访18个年末,最后一次随访于2018年11年末22日。病患的咳嗽在FMT后一个年末明显好转,大日后周内增大至每日1-2次,食欲强化,腹心痛、烦症形如不复体现发挥作用。躁郁症形如也备受益了强化,汉密尔顿焦虑症量表(HAM-D17)评价由30分回升13分。BMI上升至18.3 kg/m2,血清体内内急剧下回升38 g/L。感到惊讶的是,虽然FMT前后没有用作任何其他疗程疣赤的药物,但是,在FMT后的第四周随访时,病患调查报告却说他的疣赤处之后长三出来原先短发,而且慢慢地的一部分白短发慢慢变黑,。最后一次访视时,他的短发保持生长三(所示2),同时颈部老人疣不复体现发挥作用(未有照片)。
讨论
我们调查报告一则有中的国老人病患,因为慢连续性咳嗽做FMT疗程后,咳嗽症形如备受益有效连续性强化的同时,疣赤处之后长三出了头发,并且原来的剑侠部分转回胡子,躁郁症形如强化,颈部老人疣不复体现发挥作用。我们推断,所有这些变化都与FMT后排泄质生物群的改变有关。排泄生态系统生理在病原咳嗽中的起着关键发挥作用[16,17]。使用FMT疗程疑为梭形如芽胞病原体系统连续性咳嗽,其抗菌甚至比不上本品或安慰剂[18]。除病原咳嗽外,排泄生态系统生理在非病原咳嗽中的也体现着举足轻重发挥作用[10-12]。一项双盲、随机、安慰剂对照、交叉一组、单中的心试验车研究成果结果显示[7],做FMT疗程后,咳嗽型大肠易激整体征症形如明显强化。在东莞医科大学国立大学自建第一疗养院FMT疗程中的心,我们用作FMT疗程了40则有咳嗽病患,所有病患的症形如除此以外备受益了明显强化(数据库未有发表撰文)。在这个确诊中的,我们对一位非病原咳嗽的老人病人进行时了FMT疗程。在疗程更进一步中的,我们惊奇地掩蔽到他病症周围的头发不可逆的情形。
疣赤的医学分型之外疣片形如疣赤、全赤和普赤[19]。其确诊一组态之外以下几个心理因素:(1)基因突变:已断定62个基因参加疣赤的确诊一组态[19];(2)抗病毒应答:抗病毒耐备受的丧失以及随后长丝自身鼓吹应连续性诱发的鼓吹击被相信是疣赤的主要形如况[1,19,20];(3)其他心理因素:氧化应激和传染因子可随之而来抗病毒耐备受的损害,引发疣赤[19,20]。此外,心理应激有可能是疣赤频发和其发展的过重心理因素,但这一观点已为体现发挥作用争议[20-23]。
疣赤的疗程方式之外几个多方面。第一,局部运用于皮质激素。但该疗程不能抑制疣赤在其他各部位的频发[1,19]。其次,成果迅速的疣赤病患可通过四肢运用于皮质类固醇而获益[19,24,25]。但是在大多数理论上,只能持续连续性的用作来保持头频发长三[19]。第三,接触抗病毒疗法对疣片形如疣赤病患有效连续性,但对全赤和泛赤[19]病患作废,而且复发率高(62%)。这理论上只能针对原先靶点进行时原先、不够有效连续性的疗程干预。
近十年,多项研究成果却说明,排泄质生态系统生理在抗原皮炎、牛皮癣等病症的确诊中的体现举足轻重发挥作用[26-29]。然而疣赤与排泄质生态系统生理的彼此间已为待详述。疣赤有可能与其他自身抗病毒连续性病症,尤其是IBD[30]有关。一系列医学确诊刊文IBD病患消失病症情形[31-34],但对其病症了解非常少。排泄质生态系统生理是IBD的主要确诊一组态之一[35-37],排泄质生态系统生理有可能是疣赤和IBD共存的共同除此以外。维他命B7是一种水溶连续性维他命,主要仰赖排泄中的的菌株造成。病症是维他命B7缺失[38]的显出之一,而这种缺失是由多种心理因素引发的,之外IBD[39]。最近,Hayashi等[2]刊文了在缺失维他命B7的无菌血清中的频发病症情形,并伴有疙瘩酸菌的过度生长三。血清在说明维他命B7后头发不可逆的,獭疙瘩病原体总数增大,却说明赤发主要是由于排泄质生态系统生理,尤其是獭疙瘩病原体过度生长三,随之而来糖类[2]缺失归因于。因此,排泄质生态系统生理和疣赤彼此之间体现发挥作用密切这样一来联系。
由排泄芽孢造成的短链羧酸(SCFAs)通过调节调节连续性T细胞(regulatory T cells, Tregs)的总数和新功能,有助于确保[40]的抗病毒稳态,Tregs在疣赤的诱导中的体现关键发挥作用[3,30]。Borde等[3]推断,SCFAs中的的乙酯灶通过刺激G肽偶联备受体,诱导造成不够多的耐备受连续性tregs,保护措施长丝免备受抗病毒鼓吹击。他们掩蔽到,5只C3H/He J血清(一种自发频发疣赤的血清)中的,在乙酯疗程11周后头发不可逆的,Treg/CD4+比则有增加。然而,当他们再度重复这项研究成果时,并没有重演短发不可逆的的积极结果。由于排泄芽孢种类多种不同,仅通过包括一种SCFAs来确保但会排泄芽孢是不够的,或许是随之而来结果不确定的形如况。然而,排泄质生态系统生理和疣赤彼此之间的寻常这样一来联系可能体现发挥作用,并且确保一个肥胖症的排泄质生态系统生存环境,而不是理论上包括几种SCFAs,将在疗程疣赤中的体现不够有效连续性的发挥作用。
维他命D是我们日常素食中的的质量营养素之一,它能确保体液中的钙和砷的但会高水平。维他命D通过活化复合物Cyp27B1[42]转化为1,25(OH)2D3的活连续性形式来体现其病理学新功能。1,25(OH)2D3通过融合维他命D备受体(VDR)从而使其保持病理学活连续性[43]。日益多的证词却说明,1,25 (OH)2D3缺失与疣赤有关[44-46],其中的VDR缺失在疣赤中的体现举足轻重发挥作用[47-49]。最近的一项研究成果却说明1,25(OH)2D3缺失随之而来排泄质生态系统生理,随之而来SCFAs造成[50]的增大。另一多方面,多项研究成果却说明VDR和Cyp27B1的表达备受排泄芽孢的管控[51-53]。因此,虽然1,25(OH)2D3与排泄芽孢彼此之间体现发挥作用双向彼此间,1,25(OH)2D3缺失与排泄芽孢松弛彼此之间有可能体现发挥作用双向彼此间[43],但已为不可信哪一种一组态是疣赤确诊的主要形如况。
FMT被相信是一种确保安全有效连续性的确保排泄质生态系统松弛的方式,对鼓吹复发作的CDI、IBD、IBS、胃溃疡等带有较差的医学抗菌[54-57]。FMT确保排泄质生态系统的方法已为未有完全详述。Ooijevaar等[58]提出有可能体现发挥作用两种除此以外,即这样一来除此以外和间接除此以外。在这样一来除此以外中的,一些有益菌和营养这样一来随着FMT河运,与病原菌恶连续性竞争,说明缺失的营养,这一更进一步与细胞内毫无彼此间。在间接除此以外中的,与细胞内系统连续性心理因素,之外抗病毒调节和机械设备屏障新功能等有关。
FMT在许多病症中的的较差的医学抗菌为疗程疣赤的包括了一种有可能的方式 [3,30]。2017年,Rebello等[59]刊文2则有病症CDI伴普发连续性病症病患在用作FMT疗程后头发不可逆的的则有子。与上述两则有确诊完全符合的是,单单疣片形如疣赤的老人病患在用作FMT疗程非病原咳嗽后消失了头发的长三期生长三(表1)。这些结果却说明,FMT可以通过说明排泄质生物群而有助于头发的不可逆的。肥胖症排泄质生物生存环境的确保有助于舰载机的抗病毒调节,强化营养的释放出和小分子,之外氨基酸/细胞内、糖类、SCFAs和维他命D,最终促进短发不可逆的。单单中的,老人病患经FMT后营养形如况有所强化,BMI和血清体内内除此以外略有急剧下降。遗憾的是,我们无法包括该病患在FMT前后的维他命B7和维他命D高水平,而这一资讯的拿到有可能有助于详述FMT随之而来头发不可逆的的一组态。
除了头发不可逆的之外,我们还断定该老人病患的白短发转回胡子的情形,而且脸上老人疣不复体现发挥作用。白短发转黑的一组态目前已为不具体。某些内脏抗原自身抗病毒连续性病症有可能参加了其中的,提示排泄芽孢有可能与白短发的转变成更进一步有关[60]。因此,该老人病患可以在确保排泄质生态系统生存环境平衡后白短发转回胡子。此外,由于排泄芽孢可以通过大肠-脑轴调节神经元和精神心理发挥作用[61,62],病患在FMT后躁郁症形如也备受益强化。
总的来却说,尽管本则有子和Rebello等的医学报导[59]除此以外断定,FMT对疣赤除此以外有较差的医学抗菌,但仍只能进行大型的设计者较差的医学试验车,再进一步推测FMT疗程疣赤的医学抗菌。
Figure 1 Colonoscopy showing a normal colonic mucosa.
Figure 2 Hair regrowth on an elderly Chinese patient’s scalp after fecal microbiota transplantation. The patient’s scalp 1 mo (A), 4 mo (B), and 18 mo (C) after fecal microbiota transplantation, respectively.
参考古籍
1 Trüeb RM, Dias MFRG. Alopecia Areata: a Comprehensive Review of Pathogenesis and Management.Clin Rev Allergy Immunol 2018; 54: 68-87 [PMID: 28717940 DOI: 10.1007/s12016-017-8620-9]
2 Hayashi A, Mikami Y, Miyamoto K, Kamada N, Sato T, Mizuno S, Naganuma M, Teratani T, Aoki R,Fukuda S, Suda W, Hattori M, Amagai M, Ohyama M, Kanai T. Intestinal Dysbiosis and Biotin
Deprivation Induce Alopecia through Overgrowth of Lactobacillus murinus in Mice. Cell Rep 2017; 20:1513-1524 [PMID:28813664 DOI: 10.1016/j.celrep.2017.07.057]
3 Borde A, Åstrand A. Alopecia areata and the gut-the link opens up for novel therapeutic interventions.Expert Opin Ther Targets 2018; 22: 503-511 [PMID: 29808708 DOI: 10.1080/14728222.2018.1481504]
4 Cammarota G, Ianiro G, Tilg H, Rajilić-Stojanović M, Kump P, Satokari R, Sokol H, Arkkila P, PintusC, Hart A, Segal J, Aloi M, Masucci L, Molinaro A, Scaldaferri F, Gasbarrini G, Lopez-Sanroman A, LinkA, de Groot P, de Vos WM, Högenauer C, Malfertheiner P, Mattila E, Milosavljević T, Nieuwdorp M,Sanguinetti M, Simren M, Gasbarrini A; European FMT Working Group. European consensus conferenceon faecal microbiota transplantation in clinical practice. Gut 2017; 66: 569-580 [PMID: 28087657 DOI:10.1136/gutjnl-2016-313017]
5 Millan B, Laffin M, Madsen K. Fecal Microbiota Transplantation: Beyond Clostridium difficile. CurrInfect Dis Rep 2017; 19: 31 [PMID: 28770495 DOI: 10.1007/s11908-017-0586-5]
6 Halkjær SI, Christensen AH, Lo BZS, Browne PD, Günther S, Hansen LH, Petersen AM. Faecal
microbiota transplantation alters gut microbiota in patients with irritable bowel syndrome: results from arandomised, double-blind placebo-controlled study. Gut 2018; 67: 2107-2115 [PMID: 29980607 DOI:10.1136/gutjnl-2018-316434]
7 Johnsen PH, Hilpüsch F, Cavanagh JP, Leikanger IS, Kolstad C, Valle PC, Goll R. Faecal microbiotatransplantation versus placebo for moderate-to-severe irritable bowel syndrome: a double-blind,randomised, placebo-controlled, parallel-group, single-centre trial. Lancet Gastroenterol Hepatol 2018; 3:17-24 [PMID: 29100842 DOI: 10.1016/s2468-1253(17)30338-2]
8 Bajaj JS, Kassam Z, Fagan A, Gavis EA, Liu E, Cox IJ, Kheradman R, Heuman D, Wang J, Gurry T,Williams R, Sikaroodi M, Fuchs M, Alm E, John B, Thacker LR, Riva A, Smith M, Taylor-Robinson SD,Gillevet PM. Fecal microbiota transplant from a rational stool donor improves hepatic encephalopathy: Arandomized clinical trial. Hepatology 2017; 66: 1727-1738 [PMID: 28586116 DOI: 10.1002/hep.29306]
9 Tian H, Ding C, Gong J, Ge X, McFarland LV, Gu L, Wei Y, Chen Q, Zhu W, Li J, Li N. Treatment of Slow Transit Constipation With Fecal Microbiota Transplantation: A Pilot Study. J Clin Gastroenterol 2016; 50: 865-870 [PMID: 26751143 DOI: 10.1097/mcg.0000000000000472]
10 Lee JR, Magruder M, Zhang L, Westblade LF, Satlin MJ, Robertson A, Edusei E, Crawford C, Ling L,Taur Y, Schluter J, Lubetzky M, Dadhania D, Pamer E, Suthanthiran M. Gut microbiota dysbiosis and diarrhea in kidney transplant recipients. Am J Transplant 2019; 19: 488-500 [PMID: 29920927 DOI:10.1111/ajt.14974]
11 Logan C, Beadsworth MB, Beeching NJ. HIV and diarrhoea: what is new? Curr Opin Infect Dis 2016; 29:486-494 [PMID: 27472290 DOI: 10.1097/qco.0000000000000305]
12 Gerassy-Vainberg S, Blatt A, Danin-Poleg Y, Gershovich K, Sabo E, Nevelsky A, Daniel S, Dahan A, Ziv O, Dheer R, Abreu MT, Koren O, Kashi Y, Chowers Y. Radiation induces proinflammatory dysbiosis:transmission of inflammatory susceptibility by host cytokine induction. Gut 2018; 67: 97-107 [PMID: 28438965 DOI: 10.1136/gutjnl-2017-313789]
13 Cui B, Li P, Xu L, Zhao Y, Wang H, Peng Z, Xu H, Xiang J, He Z, Zhang T, Nie Y, Wu K, Fan D, Ji G, Zhang F. Step-up fecal microbiota transplantation strategy: a pilot study for steroid-dependent ulcerative colitis. J Transl Med 2015; 13: 298 [PMID: 26363929 DOI: 10.1186/s12967-015-0646-2]
14 Cui B, Feng Q, Wang H, Wang M, Peng Z, Li P, Huang G, Liu Z, Wu P, Fan Z, Ji G, Wang X, Wu K, Fan D, Zhang F. Fecal microbiota transplantation through mid-gut for refractory Crohn's disease: safety, feasibility, and efficacy trial results. J Gastroenterol Hepatol 2015; 30: 51-58 [PMID: 25168749 DOI: 10.1111/jgh.12727]
15 Bech P, Kastrup M, Rafaelsen OJ. Mini-compendium of rating scales for states of anxiety depression mania schizophrenia with corresponding DSM-III syndromes. Acta Psychiatr Scand Suppl 1986; 326: 1-37 [PMID: 3458353]
16 Sarker SA, Ahmed T, Brüssow H. Persistent diarrhea: a persistent infection with enteropathogens or a gut commensal dysbiosis? Environ Microbiol 2017; 19: 3789-3801 [PMID: 28752952 DOI: 10.1111/1462-2920.13873]
17 Battaglioli EJ, Hale VL, Chen J, Jeraldo P, Ruiz-Mojica C, Schmidt BA, Rekdal VM, Till LM, Huq L,Smits SA, Moor WJ, Jones-Hall Y, Smyrk T, Khanna S, Pardi DS, Grover M, Patel R, Chia N, Nelson H, Sonnenburg JL, Farrugia G, Kashyap PC. Clostridioides difficile uses amino acids associated with gut microbial dysbiosis in a subset of patients with diarrhea. Sci Transl Med 2018; 10: eaam7019 [PMID: 30355801 DOI: 10.1126/scitranslmed.aam7019]
18 Moayyedi P, Yuan Y, Baharith H, Ford AC. Faecal microbiota transplantation for Clostridium difficileassociated diarrhoea: a systematic review of randomised controlled trials. Med J Aust 2017; 207: 166-172 [PMID: 28814204 DOI: 10.5694/mja17.00295]
19 Pratt CH, King LE, Messenger AG, Christiano AM, Sundberg JP. Alopecia areata. Nat Rev Dis Primers 2017; 3: 17011 [PMID: 28300084 DOI: 10.1038/nrdp.2017.11]
20 Simakou T, Butcher JP, Reid S, Henriquez FL. Alopecia areata: A multifactorial autoimmune condition. J Autoimmun 2019; 98: 74-85 [PMID: 30558963 DOI: 10.1016/j.jaut.2018.12.001]
21 Manolache L, Petrescu-Seceleanu D, Benea V. Alopecia areata and relationship with stressful events in children. J Eur Acad Dermatol Venereol 2009; 23: 107-109 [PMID: 18410331 DOI: 10.1111/j.1468-3083.2008.02748.x]
22 Manolache L, Benea V. Stress in patients with alopecia areata and vitiligo. J Eur Acad Dermatol Venereol 2007; 21: 921-928 [PMID: 17659001 DOI: 10.1111/j.1468-3083.2006.02106.x]
23 Picardi A, Pasquini P, Cattaruzza MS, Gaetano P, Baliva G, Melchi CF, Papi M, Camaioni D, Tiago A, Gobello T, Biondi M. Psychosomatic factors in first-onset alopecia areata. Psychosomatics 2003; 44: 374- 381 [PMID: 12954911 DOI: 10.1176/appi.psy.44.5.374]
24 Nakajima T, Inui S, Itami S. Pulse corticosteroid therapy for alopecia areata: study of 139 patients. Dermatology 2007; 215: 320-324 [PMID: 17911990 DOI: 10.1159/000107626]
25 Yang CC, Lee CT, Hsu CK, Lee YP, Wong TW, Chao SC, Lee JY, Sheu HM, Chen W. Early intervention with high-dose steroid pulse therapy prolongs disease-free interval of severe alopecia areata: a retrospective study. Ann Dermatol 2013; 25: 471-474 [PMID: 24371395 DOI: 10.5021/ad.2013.25.4.471]
26 Penders J, Stobberingh EE, van den Brandt PA, Thijs C. The role of the intestinal microbiota in the development of atopic disorders. Allergy 2007; 62: 1223-1236 [PMID: 17711557 DOI: 10.1111/j.1398-9995.2007.01462.x]
27 Scher JU, Ubeda C, Artacho A, Attur M, Isaac S, Reddy SM, Marmon S, Neimann A, Brusca S, Patel T, Manasson J, Pamer EG, Littman DR, Abramson SB. Decreased bacterial diversity characterizes the altered gut microbiota in patients with psoriatic arthritis, resembling dysbiosis in inflammatory bowel disease. Arthritis Rheumatol 2015; 67: 128-139 [PMID: 25319745 DOI: 10.1002/art.38892]
28 Song H, Yoo Y, Hwang J, Na YC, Kim HS. Faecalibacterium prausnitzii subspecies-level dysbiosis in the human gut microbiome underlying atopic dermatitis. J Allergy Clin Immunol 2016; 137: 852-860 [PMID: 26431583 DOI: 10.1016/j.jaci.2015.08.021]
29 Visser MJE, Kell DB, Pretorius E. Bacterial Dysbiosis and Translocation in Psoriasis Vulgaris. Front Cell Infect Microbiol 2019; 9: 7 [PMID: 30778377 DOI: 10.3389/fcimb.2019.00007]
30 Skogberg G, Jackson S, Åstrand A. Mechanisms of tolerance and potential therapeutic interventions in Alopecia Areata. Pharmacol Ther 2017; 179: 102-110 [PMID: 28546083 DOI:
10.1016/j.pharmthera.2017.05.008]
31 Safina DD, Abdulkhakov RA, Abdulkhakov SR, Odintsova AKh, Cheremina NA. [Clinical case of a combination of ulcerative colitis and alopecia areata]. Eksp Klin Gastroenterol 2013; 92-96 [PMID: 24933997]
32 Treem WR, Veligati LN, Rotter JI, Targan SR, Hyams JS. Ulcerative colitis and total alopecia in a mother and her son. Gastroenterology 1993; 104: 1187-1191 [PMID: 8462807]
33 Patel KV, Farrant P, Sanderson JD, Irving PM. Hair loss in patients with inflammatory bowel disease. Inflamm Bowel Dis 2013; 19: 1753-1763 [PMID: 23624889 DOI: 10.1097/MIB.0b013e31828132de]
34 Sobolewska-Włodarczyk A, Włodarczyk M, Fichna J, Wiśniewska-Jarosińska M. Alopecia areata in patients with inflammatory bowel disease: an overview. Folia Med Cracov 2016; 56: 5-12 [PMID: 27513834]
35 Ramos GP, Papadakis KA. Mechanisms of Disease: Inflammatory Bowel Diseases. Mayo Clin Proc 2019; 94: 155-165 [PMID: 30611442 DOI: 10.1016/j.mayocp.2018.09.013]
36 Sartor RB, Wu GD. Roles for Intestinal Bacteria, Viruses, and Fungi in Pathogenesis of Inflammatory Bowel Diseases and Therapeutic Approaches. Gastroenterology 2017; 152: 327-339.e4 [PMID: 27769810 DOI: 10.1053/j.gastro.2016.10.012]
37 Rapozo DC, Bernardazzi C, de Souza HS. Diet and microbiota in inflammatory bowel disease: The gut in disharmony. World J Gastroenterol 2017; 23: 2124-2140 [PMID: 28405140 DOI: 10.3748/wjg.v23.i12.2124]
38 Zempleni J, Hassan YI, Wijeratne SS. Biotin and biotinidase deficiency. Expert Rev Endocrinol Metab2008; 3: 715-724 [PMID: 19727438 DOI: 10.1586/17446651.3.6.715]
39 Fernandez-Banares F, Abad-Lacruz A, Xiol X, Gine JJ, Dolz C, Cabre E, Esteve M, Gonzalez-Huix F, Gassull MA. Vitamin status in patients with inflammatory bowel disease. Am J Gastroenterol 1989; 84: 744-748 [PMID: 2500847]
40 Maslowski KM, Mackay CR. Diet, gut microbiota and immune responses. Nat Immunol 2011; 12: 5-9 [PMID: 21169997 DOI: 10.1038/ni0111-5]
41 Lieben L, Carmeliet G. Vitamin D signaling in osteocytes: effects on bone and mineral homeostasis. Bone 2013; 54: 237-243 [PMID: 23072922 DOI: 10.1016/j.bone.2012.10.007]
42 Fraser DR, Kodicek E. Unique biosynthesis by kidney of a biological active vitamin D metabolite. Nature 1970; 228: 764-766 [PMID: 4319631 DOI: 10.1038/228764a0]
43 Singh P, Kumar M, Al Khodor S. Vitamin D Deficiency in the Gulf Cooperation Council: Exploring the Triad of Genetic Predisposition, the Gut Microbiome and the Immune System. Front Immunol 2019; 10: 1042 [PMID: 31134092 DOI: 10.3389/fimmu.2019.01042]
44 Thompson JM, Mirza MA, Park MK, Qureshi AA, Cho E. The Role of Micronutrients in Alopecia Areata: A Review. Am J Clin Dermatol 2017; 18: 663-679 [PMID: 28508256 DOI: 10.1007/s40257-017-0285-x]
45 Tsai TY, Huang YC. Vitamin D deficiency in patients with alopecia areata: A systematic review and meta-analysis. J Am Acad Dermatol 2018; 78: 207-209 [PMID: 29241789 DOI: 10.1016/j.jaad.2017.07.051]
46 Lee S, Kim BJ, Lee CH, Lee WS. Increased prevalence of vitamin D deficiency in patients with alopecia areata: a systematic review and meta-analysis. J Eur Acad Dermatol Venereol 2018; 32: 1214-1221 [PMID: 29633370 DOI: 10.1111/jdv.14987]
47 Chen CH, Sakai Y, Demay MB. Targeting expression of the human vitamin D receptor to the
keratinocytes of vitamin D receptor null mice prevents alopecia. Endocrinology 2001; 142: 5386-5389 [PMID: 11713240 DOI: 10.1210/endo.142.12.8650]
48 Xie Z, Komuves L, Yu QC, Elalieh H, Ng DC, Leary C, Chang S, Crumrine D, Yoshizawa T, Kato S, Bikle DD. Lack of the vitamin D receptor is associated with reduced epidermal differentiation and hair follicle growth. J Invest Dermatol 2002; 118: 11-16 [PMID: 11851870 DOI:
10.1046/j.1523-1747.2002.01644.x]
49 Fawzi MM, Mahmoud SB, Ahmed SF, Shaker OG. Assessment of vitamin D receptors in alopecia areata and androgenetic alopecia. J Cosmet Dermatol 2016; 15: 318-323 [PMID: 27151518 DOI: 10.1111/jocd.12224]
50 Zhu W, Yan J, Zhi C, Zhou Q, Yuan X. 1,25(OH) 2D3 deficiency-induced gut microbial dysbiosis degrades the colonic mucus barrier in Cyp27b1 knockout mouse model. Gut Pathog 2019; 11: 8 [PMID: 30828386 DOI: 10.1186/s13099-019-0291-z]
51 Waterhouse JC, Perez TH, Albert PJ. Reversing bacteria-induced vitamin D receptor dysfunction is key to autoimmune disease. Ann N Y Acad Sci 2009; 1173: 757-765 [PMID: 19758226 DOI: 10.1111/j.1749-6632.2009.04637.x]
52 Appleyard CB, Cruz ML, Isidro AA, Arthur JC, Jobin C, De Simone C. Pretreatment with the probiotic VSL#3 delays transition from inflammation to dysplasia in a rat model of colitis-associated cancer. Am J Physiol Gastrointest Liver Physiol 2011; 301: G1004-G1013 [PMID: 21903764 DOI:
10.1152/ajpgi.00167.2011]
53 Mukherji A, Kobiita A, Ye T, Chambon P. Homeostasis in intestinal epithelium is orchestrated by the circadian clock and microbiota cues transduced by TLRs. Cell 2013; 153: 812-827 [PMID: 23663780 DOI: 10.1016/j.cell.2013.04.020]
54 Hvas CL, Dahl Jørgensen SM, Jørgensen SP, Storgaard M, Lemming L, Hansen MM, Erikstrup C, Dahlerup JF. Fecal Microbiota Transplantation Is Superior to Fidaxomicin for Treatment of Recurrent Clostridium difficile Infection. Gastroenterology 2019; 156: 1324-1332.e3 [PMID: 30610862 DOI: 10.1053/j.gastro.2018.12.019]
55 Chen D, Wu J, Jin D, Wang B, Cao H. Fecal microbiota transplantation in cancer management: Current status and perspectives. Int J Cancer 2019; 145: 2021-2031 [PMID: 30458058 DOI: 10.1002/ijc.32003]
56 Borody T, Fischer M, Mitchell S, Campbell J. Fecal microbiota transplantation in gastrointestinal disease: 2015 update and the road ahead. Expert Rev Gastroenterol Hepatol 2015; 9: 1379-1391 [PMID: 26414076 DOI: 10.1586/17474124.2015.1086267]
57 Xie WR, Yang XX, Xia HHX, He XX. Fecal microbiota transplantation for treating hepatic
encephalopathy: Experimental and clinical evidence and possible underlying mechanisms. J Explor Res Pharmacol 2018; 3: 119-124 [DOI: 10.14218/JERP.2018.00017]
58 Ooijevaar RE, Terveer EM, Verspaget HW, Kuijper EJ, Keller JJ. Clinical Application and Potential of Fecal Microbiota Transplantation. Annu Rev Med 2019; 70: 335-351 [PMID: 30403550 DOI: 10.1146/annurev-med-111717-122956]
59 Rebello D, Wang E, Yen E, Lio PA, Kelly CR. Hair Growth in Two Alopecia Patients after Fecal Microbiota Transplant. ACG Case Rep J 2017; 4: e107 [PMID: 28932754 DOI: 10.14309/crj.2017.107]
60 Pandhi D, Khanna D. Premature graying of hair. Indian J Dermatol Venereol Leprol 2013; 79: 641-653 [PMID: 23974581 DOI: 10.4103/0378-6323.116733]
61 Kuty-Pachecka M. Psychological and psychopathological factors in alopecia areata. Psychiatr Pol 2015; 49: 955-964 [PMID: 26688846 DOI: 10.12740/pp/39064]
62 Groen RN, de Clercq NC, Nieuwdorp M, Hoenders HJR, Groen AK. Gut microbiota, metabolism and psychopathology: A critical review and novel perspectives. Crit Rev Clin Lab Sci 2018; 55: 283-293 [PMID: 29673295 DOI: 10.1080/10408363.2018.1463507]
附件2 英文名称的摘要链接
干净芽孢再生(washed microbiota transplantation, WMT)
东莞医科大学国立大学自建第一疗养院消化内科自成立质生态系统疗程中的心以来,年末于2022年4年末30日,完毕WMT 6200 人次,其中的前十病种分别为:新开放连续性胃大肠病1693人次、儿童帕金森氏症1871人次、菌株连续性大肠病635人次、胃食管鼓吹流病420人次、非酒精连续性脂肪肝连续性胃溃疡178人次、胃癌失代偿期132人次、排泄芽孢生理369人次、心关节炎137人次、2型哮喘403人次以及皮肤类病症(银屑病、荨麻疹、皮疹皮炎、特应连续性皮炎和病症)120人次,除此以外拿到了情愿的医学抗菌。能用干净质生物群再生可以疗程本内脏(排泄质生物群这个类似于的内脏)结构及新功能损毁诱发的系统连续性病症,不仅在昆虫物理中的拿到了获得成功,而且在医学上也拿到了情愿的抗菌。
本中的心进行的WMT处于亚太地区主导地位,先后接收Rebiotix和Ferring研究成果所、北京阜外疗养院、岳皓市中的疗养院、成都中的医药国立大学自建疗养院、南方医科国立大学自建珠江疗养院等25家疗养院参观及进修自学,并对其进行时医学干净芽孢再生指导工作,使其获得成功建立了芽孢再生医学运用于与研究成果基地,同时作为周围救援队中的心,向救援队合作为单位中的文系自建第一疗养院、广州医科国立大学第一自建疗养院、广州医科国立大学第二自建疗养院、暨南国立大学自建东亚红十字会疗养院、锡林郭勒盟鄂温克旗疗养院等12个为单位进行时了干净芽孢再生救援队工作,并备受益了相鼓吹的赞誉。
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