Sex and Gender in Glomerular Disease

The Descent of Man, and Selection in Relation to Sex.

Murray, LondonBairey Merz CN Dember LM Ingelfinger JR et al.

Sex and the kidneys: current understanding and research opportunities.

Nat Rev Nephrol. 15: 776-783https://doi.org/10.1038/s41581-019-0208-6

Organisation WH. Gender and Health, https://www.who.int/health-topics/gender#tab=tab_1 (accessed 22/12/2021 2021).

Oxford Textbook of Medicine. 6 ed: Oxford University Press, 2020.

O'Shaughnessy MM Hogan SL Thompson BD et al.

Glomerular disease frequencies by race, sex and region: results from the International Kidney Biopsy Survey. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association.

European Renal Association. 33 (): 661-669https://doi.org/10.1093/ndt/gfx189

The New Zealand Glomerulonephritis Study: introductory report.

Clinical nephrology. 31: 239-246

Cattran DC, Reich HN, Beanlands HJ, et al. The impact of sex in primary glomerulonephritis. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 2008;23:2247-2253. 2008/01/10. https://doi.org/10.1093/ndt/gfm919.

Deng W Tan X Zhou Q et al.

Gender-related differences in clinicopathological characteristics and renal outcomes of Chinese patients with IgA nephropathy.

BMC Nephrol. 19 (): 31https://doi.org/10.1186/s12882-018-0829-1Sandberg K Pai AV Maddox T.

Sex and rigor: the TGF-β blood pressure affair.

Am J Physiol Renal Physiol. 313 (): F1087-f1088https://doi.org/10.1152/ajprenal.00381.2017Ricardo AC Yang W Sha D et al.

Sex-Related Disparities in CKD Progression.

Journal of the American Society of Nephrology: JASN. 30 (): 137-146https://doi.org/10.1681/asn.2018030296

Sex differences in autoimmune disease.

Nat Immunol. 2 (): 777-780https://doi.org/10.1038/ni0901-777Billi AC Kahlenberg JM Gudjonsson JE.

Sex bias in autoimmunity.

Curr Opin Rheumatol. 31 (): 53-61https://doi.org/10.1097/bor.0000000000000564Lim SS Bayakly AR Helmick CG et al.

The incidence and prevalence of systemic lupus erythematosus, 2002-2004: The Georgia Lupus Registry.

Arthritis & rheumatology (Hoboken, NJ). 66 (): 357-368https://doi.org/10.1002/art.38239Batocchi AP Majolini L Evoli A et al.

Course and treatment of myasthenia gravis during pregnancy.

Neurology. 52 (): 447-452https://doi.org/10.1212/wnl.52.3.447

Management of pregnancy in systemic lupus erythematosus.

Nat Rev Rheumatol. 8 (): 710-718https://doi.org/10.1038/nrrheum.2012.133Billip-Tomecka Z Gellert R Zaleska M et al.

[Renal biopsy in the aged].

Biopsja nerki u osob w wieku podeszlym. 89: 335-341

The Gut-Renal Connection in IgA Nephropathy.

Semin Nephrol. 38 (): 504-512https://doi.org/10.1016/j.semnephrol.2018.05.020

Sex differences in immune responses.

Nat Rev Immunol. 16 (): 626-638https://doi.org/10.1038/nri.2016.90Lissauer D Eldershaw SA Inman CF et al.

Progesterone promotes maternal-fetal tolerance by reducing human maternal T-cell polyfunctionality and inducing a specific cytokine profile.

Eur J Immunol. 45 (): 2858-2872https://doi.org/10.1002/eji.201445404Dragin N Bismuth J Cizeron-Clairac G et al.

Estrogen-mediated downregulation of AIRE influences sexual dimorphism in autoimmune diseases.

J Clin Invest. 126 (): 1525-1537https://doi.org/10.1172/jci81894

Estrogen receptors regulate innate immune cells and signaling pathways.

Cell Immunol. 294 (): 63-69https://doi.org/10.1016/j.cellimm.2015.01.018Bereshchenko O Bruscoli S Glucocorticoids Riccardi C. Sex Hormones, and Immunity. Front Immunol. 9 (): 1332https://doi.org/10.3389/fimmu.2018.01332Hao S Zhao J Zhou J et al.

Modulation of 17beta-estradiol on the number and cytotoxicity of NK cells in vivo related to MCM and activating receptors.

Int Immunopharmacol. 7 (): 1765-1775https://doi.org/10.1016/j.intimp.2007.09.017Karpuzoglu E Phillips RA Gogal Jr, RM et al.

IFN-gamma-inducing transcription factor, T-bet is upregulated by estrogen in murine splenocytes: role of IL-27 but not IL-12.

Mol Immunol. 44 (): 1808-1814Cunningham MA Wirth JR Scott JL et al.

Early Ovariectomy Results in Reduced Numbers of CD11c+/CD11b+ Spleen Cells and Impacts Disease Expression in Murine Lupus.

Front Immunol. 7 (): 31https://doi.org/10.3389/fimmu.2016.00031Trigunaite A Dimo J Jørgensen TN.

Suppressive effects of androgens on the immune system.

Cell Immunol. 294 (): 87-94https://doi.org/10.1016/j.cellimm.2015.02.004Zhu ML Bakhru P Conley B et al.

Sex bias in CNS autoimmune disease mediated by androgen control of autoimmune regulator.

Nat Commun. 7 (): 11350https://doi.org/10.1038/ncomms11350Borba VV Zandman-Goddard G Shoenfeld Y. Prolactin and Autoimmunity. Front Immunol. 9 (): 73https://doi.org/10.3389/fimmu.2018.00073

Circulating prolactin level in systemic lupus erythematosus and its correlation with disease activity: a meta-analysis.

Lupus. 26 (): 1260-1268https://doi.org/10.1177/0961203317693094Scofield RH Bruner GR Namjou B et al.

Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: support for the notion of a gene-dose effect from the X chromosome.

Arthritis and rheumatism. 58 (): 2511-2517https://doi.org/10.1002/art.23701Lam IKY Chow JX Lau CS et al.

MicroRNA-mediated immune regulation in rheumatic diseases.

Cancer Lett. 431 (): 201-212https://doi.org/10.1016/j.canlet.2018.05.044Hewagama A Gorelik G Patel D et al.

Overexpression of X-linked genes in T cells from women with lupus.

J Autoimmun. 41 (): 60-71https://doi.org/10.1016/j.jaut.2012.12.006Pickard JM Zeng MY Caruso R et al.

Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease.

Immunol Rev. 279 (): 70-89https://doi.org/10.1111/imr.12567Markle JG Frank DN Mortin-Toth S et al.

Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity.

Science. 339 (): 1084-1088https://doi.org/10.1126/science.1233521Tanaka R Tsutsui H Kobuchi S et al.

Protective effect of 17β-estradiol on ischemic acute kidney injury through the renal sympathetic nervous system.

Eur J Pharmacol. 683 (): 270-275https://doi.org/10.1016/j.ejphar.2012.02.044Mankhey RW Bhatti F Maric C.

17beta-Estradiol replacement improves renal function and pathology associated with diabetic nephropathy.

Am J Physiol Renal Physiol. 288 (): F399-F405Sakemi T Toyoshima H Shouno Y et al.

Estrogen attenuates progressive glomerular injury in hypercholesterolemic male Imai rats.

Nephron. 69 (): 159-165https://doi.org/10.1159/000188433Corradetti C Jog NR Cesaroni M et al.

Estrogen Receptor alpha Signaling Exacerbates Immune-Mediated Nephropathies through Alteration of Metabolic Activity.

Journal of immunology (Baltimore, Md : 1950). 200: 512-522https://doi.org/10.4049/jimmunol.1700770Fortepiani LA Yanes L Zhang H et al.

Role of androgens in mediating renal injury in aging SHR.

Hypertension. 42 (): 952-955https://doi.org/10.1161/01.Hyp.0000099241.53121.7f

Sex chromosome effects unmasked in angiotensin II-induced hypertension.

Hypertension. 55 (): 1275-1282https://doi.org/10.1161/hypertensionaha.109.144949De La Mata NL Rosales B MacLeod G et al.

Sex differences in mortality among binational cohort of people with chronic kidney disease: population based data linkage study.

BMJ. 375e068247https://doi.org/10.1136/BMJ-2021-068247Canetta PA Troost JP Mahoney S et al.

Health-related quality of life in glomerular disease.

Kidney international. 95 (): 1209-1224https://doi.org/10.1016/j.kint.2018.12.018Phyo AZZ Freak-Poli R Craig H et al.

Quality of life and mortality in the general population: a systematic review and meta-analysis.

BMC Public Health. 20: 1596https://doi.org/10.1186/s12889-020-09639-9Mahr N Neyer U Prischl F et al.

Proteinuria and hemoglobin levels in patients with primary glomerular disease.

American journal of kidney diseases: the official journal of the National Kidney Foundation. 46: 424-431

Coggins CH, Breyer Lewis J, Caggiula AW, et al. Differences between women and men with chronic renal disease. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association 1998;13:1430-1437. 1998/06/26. https://doi.org/10.1093/ndt/13.6.1430.

Gender differences in the regulation of blood pressure.

Hypertension. 37 (): 1199-1208https://doi.org/10.1161/01.hyp.37.5.1199Ronkainen J Nuutinen M Koskimies O.

The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study.

Lancet (London, England). 360 (): 666-670https://doi.org/10.1016/s0140-6736(02)09835-5Nakamura I Iwase H Arai K et al.

Detection of gender difference and epitope specificity of IgG antibody activity against IgA1 hinge portion in IgA nephropathy patients by using synthetic hinge peptide and glycopeptide probes.

Nephrology (Carlton, Vic). 9 (): 26-30https://doi.org/10.1111/j.1440-1797.2003.00225.xMagistroni R D’Agati VD Appel GB Kiryluk K

New developments in the genetics, pathogenesis, and therapy of IgA nephropathy.

Kidney Int. 88: 974-989

3′UTR variants of TNS3, PHLDB1, NTN4, and GNG2 genes are associated with IgA nephropathy risk in Chinese Han population.

International immunopharmacology. 71: 295-300https://doi.org/10.1016/j.intimp.2019.03.041Cattran DC Reich HN Beanlands HJ et al.

The impact of sex in primary glomerulonephritis.

Nephrology Dialysis Transplantation. 23: 2247-2253https://doi.org/10.1093/ndt/gfm919Goto M Wakai K Kawamura T et al.

A scoring system to predict renal outcome in IgA nephropathy: a nationwide 10-year prospective cohort study. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association.

European Renal Association. 24 (): 3068-3074https://doi.org/10.1093/ndt/gfp273Moriyama T Tanaka K Iwasaki C et al.

Prognosis in IgA nephropathy: 30-year analysis of 1,012 patients at a single center in Japan.

PLoS One. 9 (): e91756https://doi.org/10.1371/journal.pone.0091756Donadio JV Bergstralh EJ Grande JP et al.

Proteinuria patterns and their association with subsequent end-stage renal disease in IgA nephropathy. Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association.

European Renal Association. 17 (): 1197-1203https://doi.org/10.1093/ndt/17.7.1197Ronco P Beck L Debiec H et al.

Membranous nephropathy.

Nature Reviews Disease Primers. 7: 69https://doi.org/10.1038/s41572-021-00303-zHogan SL Muller KE Jennette JC et al.

A review of therapeutic studies of idiopathic membranous glomerulopathy.

Am J Kidney Dis. 25 (): 862-875https://doi.org/10.1016/0272-6386(95)90568-5Lee H Yoo KD Oh YK et al.

Predictors of Relapse in Adult-Onset Nephrotic Minimal Change Disease.

Medicine. 95 (): e3179https://doi.org/10.1097/md.0000000000003179Fenton A Smith SW Hewins P.

Adult minimal-change disease: observational data from a UK centre on patient characteristics, therapies, and outcomes.

BMC Nephrol. 19 (): 207https://doi.org/10.1186/s12882-018-0999-xTroyanov S Wall CA Miller JA et al.

Focal and segmental glomerulosclerosis: definition and relevance of a partial remission.

Journal of the American Society of Nephrology. 16 (): 1061-1068https://doi.org/10.1681/asn.2004070593

A follow up study of adult nephrotic syndrome in Nigerians: outcome and predictors of endstage renal failure.

African journal of medicine and medical sciences. 22: 43-50Moroni G Gallelli B Quaglini S et al.

Long-term outcome of renal transplantation in adults with focal segmental glomerulosclerosis. Transplant international : official journal of the European Society for.

Organ Transplantation. 23: 208-216https://doi.org/10.1111/j.1432-2277.2009.00977.xKashgary A Sontrop JM Li L et al.

The role of plasma exchange in treating post-transplant focal segmental glomerulosclerosis: A systematic review and meta-analysis of 77 case-reports and case-series.

BMC nephrology. 17: 104https://doi.org/10.1186/s12882-016-0322-7

Landmark publication from The American Journal of the Medical Sciences: The significance of certain pulmonary lesions in relation to the etiology of influenza.

Am J Med Sci. 338 (): 148-151https://doi.org/10.1097/MAJ.0b013e31818fff94van Daalen EE Jennette JC McAdoo SP et al.

Predicting Outcome in Patients with Anti-GBM Glomerulonephritis.

Clinical Journal of the American Society of Nephrology. 13: 63https://doi.org/10.2215/CJN.04290417

Anti-Glomerular Basement Membrane Disease.

Journal of the American Society of Nephrology. 10: 2446-2453https://doi.org/10.1681/asn.V10112446

Cigarette smoking and lung haemorrhage in glomerulonephritis caused by autoantibodies to glomerular basement membrane.

Lancet (London, England). 2 (): 1390-1393https://doi.org/10.1016/s0140-6736(83)90923-6

The association between hydrocarbon exposure and anti-glomerular basement membrane antibody-mediated disease (Goodpasture's syndrome).

Am J Ind Med. 21 (): 141-153https://doi.org/10.1002/ajim.4700210204

Anti-Glomerular Basement Membrane Disease.

Clinical journal of the American Society of Nephrology. 12 (): 1162-1172https://doi.org/10.2215/cjn.01380217Johnson CM Wilson DM O'Fallon WM et al.

Renal stone epidemiology: a 25-year study in Rochester, Minnesota.

Kidney international. 16 (): 624-631https://doi.org/10.1038/ki.1979.173McAdoo SP Tanna A Hrušková Z et al.

Patients double-seropositive for ANCA and anti-GBM antibodies have varied renal survival, frequency of relapse, and outcomes compared to single-seropositive patients.

Kidney international. 92 (): 693-702https://doi.org/10.1016/j.kint.2017.03.014Shaharir SS Kadir WDA Nordin F et al.

Systemic lupus erythematosus among male patients in Malaysia: how are we different from other geographical regions?.

Lupus. 28: 137-144https://doi.org/10.1177/0961203318812676Riveros Frutos A Casas I Rua-Figueroa I et al.

Systemic lupus erythematosus in Spanish males: a study of the Spanish Rheumatology Society Lupus Registry (RELESSER) cohort.

Lupus. 26: 698-706https://doi.org/10.1177/0961203316673728Okpechi IG Swanepoel CR Tiffin N et al.

Clinicopathological insights into lupus nephritis in South Africans: a study of 251 patients.

Lupus. 21: 1017-1024https://doi.org/10.1177/0961203312441981Peng W Tang Y Tan L et al.

Clinicopathological study of male and female patients with lupus nephritis: a retrospective study.

International urology and nephrology. 50: 313-320https://doi.org/10.1007/s11255-017-1780-ySoni SS Gowrishankar S Adikey GK et al.

Sex-based differences in lupus nephritis: a study of 235 Indian patients.

J Nephrol. 21 (): 570-575Ichinose K Kitamura M Sato S et al.

Factors predictive of long-term mortality in lupus nephritis: a multicenter retrospective study of a Japanese cohort.

Lupus. 28: 295-303https://doi.org/10.1177/0961203319826690Resende AL Titan SM Barros RT et al.

Worse renal outcome of lupus nephritis in male patients: a case-control study.

Lupus. 20: 561-567https://doi.org/10.1177/0961203310392422Feldman CH Broder A Guan H et al.

Sex Differences in Health Care Utilization, End-Stage Renal Disease, and Mortality Among Medicaid Beneficiaries With Incident Lupus Nephritis.

Arthritis & rheumatology (Hoboken, NJ). 70: 417-426https://doi.org/10.1002/art.40392Houssiau FA Vasconcelos C D'Cruz D et al.

Early response to immunosuppressive therapy predicts good renal outcome in lupus nephritis: lessons from long-term followup of patients in the Euro-Lupus Nephritis Trial.

Arthritis and rheumatism. 50 (): 3934-3940https://doi.org/10.1002/art.20666

Rapidly progressive crescentic glomerulonephritis.

Kidney international. 63 (): 1164-1177https://doi.org/10.1046/j.1523-1755.2003.00843.xHoganson DD From AM Michet CJ.

ANCA vasculitis in the elderly.

Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases. 14: 78-81https://doi.org/10.1097/RHU.0b013e31816b2fbdOno N Niiro H Ueda A et al.

Characteristics of MPO-ANCA-positive granulomatosis with polyangiitis: a retrospective multi-center study in Japan.

Rheumatology international. 35: 555-559https://doi.org/10.1007/s00296-014-3106-zBartfai Z Gaede KI Russell KA et al.

Different gender-associated genotype risks of Wegener's granulomatosis and microscopic polyangiitis.

Clinical immunology (Orlando, Fla). 109: 330-337Reynolds WF Stegeman CA Cohen Tervaert JW

−463 G/A Myeloperoxidase Promoter Polymorphism Is Associated with Clinical Manifestations and the Course of Disease in MPO-ANCA-Associated Vasculitis.

Clinical Immunology. 103: 154-160https://doi.org/10.1006/clim.2002.5206Tampe D Korsten P Ströbel P et al.

Comprehensive Analysis of Sex Differences at Disease Manifestation in ANCA-Associated Glomerulonephritis.

Front Immunol. 12 ()736638https://doi.org/10.3389/fimmu.2021.736638Scott J Canepa C Buettner A et al.

A cohort study to investigate sex-specific differences in ANCA-associated glomerulonephritis outcomes.

Sci Rep. 11 (): 13080https://doi.org/10.1038/s41598-021-92629-7Bjørneklett R Solbakken V Bostad L et al.

Exploring sex-specific differences in the presentation and outcomes of ANCA-associated vasculitis: a nationwide registry-based cohort study.

International urology and nephrology. 50 (): 1311-1318https://doi.org/10.1007/s11255-018-1888-8Takala JH Kautiainen H Leirisalo-Repo M.

Survival of patients with Wegener's granulomatosis diagnosed in Finland in 1981-2000.

Scandinavian journal of rheumatology. 39: 71-76https://doi.org/10.3109/03009740903140701Bakoush O Segelmark M Torffvit O et al.

Urine IgM excretion predicts outcome in ANCA-associated renal vasculitis. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association.

European Renal Association. 21: 1263-1269Carpenter DM DeVellis RF Hogan SL et al.

Use and perceived credibility of medication information sources for patients with a rare illness: differences by gender.

Journal of health communication. 16: 629-642https://doi.org/10.1080/10810730.2011.551995Ahearn P Johansen KL Tan JC et al.

Sex Disparity in Deceased-Donor Kidney Transplant Access by Cause of Kidney Disease.

Clinical journal of the American Society of Nephrology: CJASN. 16 (): 241-250https://doi.org/10.2215/cjn.09140620Stengel B Cenee S Limasset JC et al.

Organic solvent exposure may increase the risk of glomerular nephropathies with chronic renal failure.

International journal of epidemiology. 24: 427-434

Hydrocarbon exposure may cause glomerulonephritis and worsen renal function: evidence based on Hill's criteria for causality.

QJM : monthly journal of the Association of Physicians. 93: 551-556Smith DL Dong X Du S et al.

A female preponderance for chemically induced lupus in SJL/J mice.

Clinical immunology (Orlando, Fla). 122: 101-107

The environment, geoepidemiology and ANCA-associated vasculitides.

Autoimmunity reviews. 9 (): A293-A298McDermott G Fu X Stone JH et al.

Association of Cigarette Smoking With Antineutrophil Cytoplasmic Antibody-Associated Vasculitis.

JAMA Intern Med. 180 (): 870-876https://doi.org/10.1001/jamainternmed.2020.0675Beaglehole R Bonita R Yach D et al.

A tobacco-free world: a call to action to phase out the sale of tobacco products by 2040.

Lancet (London, England). 385 (): 1011-1018https://doi.org/10.1016/s0140-6736(15)60133-7

Drug-induced anti-neutrophil cytoplasmic antibody-associated vasculitis.

Chin Med J (Engl). 132 (): 2848-2855https://doi.org/10.1097/cm9.0000000000000539McGrath MM Isakova T Rennke HG et al.

Contaminated cocaine and antineutrophil cytoplasmic antibody-associated disease.

Clinical journal of the American Society of Nephrology: CJASN. 6 (): 2799-2805https://doi.org/10.2215/cjn.03440411Requena-Ocaña N Flores-Lopez M Martín AS et al.

Influence of gender and education on cocaine users in an outpatient cohort in Spain.

Sci Rep. 11 (): 20928https://doi.org/10.1038/s41598-021-00472-7Manteuffel M Williams S Chen W et al.

Influence of patient sex and gender on medication use, adherence, and prescribing alignment with guidelines.

J Womens Health (Larchmt). 23 (): 112-119https://doi.org/10.1089/jwh.2012.3972

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