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AUTOIMMUNE DISEASES A-Z List

Autoimmune Diseases List

The enclosed Autoimmune Diseases List (A-Z) is a compilation of autoimmune diseases from various medical and research centres, recognised around the world.

Sources

Autoimmune.org (Autoimmune Association) 

Autoimmuneinstitute.org (Global Autoimmune Institute)

The National Institutes of Health (NIH) Genetic and Rare Diseases Information Center (GARD)

The National Center for Biotechnology Information (National Library of Medicine)

PMC - PubMed Central 

Mayo Clinic

Mayo Foundation for Medical Education and Research (MFMER)

American Thoracic Society

Sjögren's Foundation

Autoimmune Diseases - A

Achalasia

Achalasia is a rare disorder that makes it difficult for food and liquid to pass into your stomach. 


Achalasia occurs when nerves in the tube connecting your mouth and stomach (esophagus) become damaged. 


As a result, the esophagus loses the ability to squeeze food down, and the muscular valve between the esophagus and stomach (lower esophageal sphincter) doesn’t fully relax — making it difficult for food to pass into your stomach. 


Source: https://www.mayoclinic.org/diseases-conditions/achalasia/symptoms-causes/syc-20352850

Acquired hemophilia

A... 

Acromegaly

A... 

Addison's disease

Where: Endocrine System


Addison’s disease is an uncommon autoimmune disease, characterized by chronic and insufficient functioning of the outer layer of the adrenal gland. 


The adrenal glands are located atop each kidney and produce vital glucocorticoid hormones. Because of this chronic under-functioning of the adrenal glands, persons with Addison’s disease have a deficiency in the production of glucocorticoid hormones. 


Glucocorticoid hormones are involved in how the body utilizes and stores carbohydrates, protein, fat and blood sugar.


The adrenal gland also plays a role in the immune response. 


A deficiency in glucocorticoid hormones causes an increase in the release of sodium and a decreased release of potassium in the urine, sweat, saliva, stomach and intestines. 


These changes can cause low blood pressure and increased water excretion that can in some cases lead to severe dehydration.


Although there are many underlying factors in the development of adrenal insufficiencies, including destruction of the adrenal cortex due to diseases such as tuberculosis, the growth of tumors, non-autoimmune diseases amyloidosis and adrenoleukodystrophy, and atrophy of the gland due to prolonged use of cortical steroids used in the treatment of other conditions and illnesses, most cases of Addison’s disease are thought to be autoimmune in nature.

Adult Still’s disease

A... 

Agammaglobulinemia

A... 

Alopecia areata

A...

Amyloidosis

A...

Ankylosing spondylitis

AS...

Anti-GBM/Anti-TBM nephritis

A...

Anti-NMDA receptor encephalitis

As...

Antiphospholipid syndrome

As...

Autoimmune Diseases - A (cont'd)

Aplastic anemia

Aa... 

Arteriosclerosis

Aa... 

Autoimmune angioedema

Aa... 

Autoimmune autonomic ganglionopathy

Ad...

Autoimmune dysautonomia

Ad...

Autoimmune encephalitis/acute disseminated encephalomyelitis

Ae...

Autoimmune gastritis

Where: Digestive System

Autoimmune hemolytic anemia

Ah...

Autoimmune hepatitis

Ah...

Autoimmune hyperlipidemia

Am...

Autoimmune hypophysitis / lymphocytic hypophysitis

Ah

Autoimmune Diseases - A (cont'd)

Autoimmune inner ear disease (AIED)

AIED


Autoimmune myocarditis

Ao...


Autoimmune oophoritis

Ao...


Autoimmune orchitis

Ao...

Autoimmune pancreatitis

Ap...

Autoimmune polyglandular syndromes

aPAP...


Autoimmune progesterone dermatitis

aPAP...


Autoimmune pulmonary alveolar proteinosis (aPAP)

aPAP...


Autoimmune retinopathy

aPAP...


Autoimmune sudden sensorineural hearing loss

aPAP...


Autoimmune urticaria

Au...

Axonal & neuronal neuropathy (AMAN)

AMAN...

Autoimmune Diseases - B

Baló’s concentric sclerosis (BCS)

Balo

Behcet’s disease

Behcet ...


Benign mucosal pemphigoid (Mucous membrane pemphigoid)

BMP...

Birdshot chorioretinopathy/birdshot uveitis

BC...

Bullous pemphigoid

BP...

Autoimmune Diseases - C

Castleman disease

C...

Celiac disease

Where: Digestive System

Chagas disease (Trypanosomiasis)

C...

Chronic inflammatory demyelinating polyneuropathy (CIDP)

Where: Nervous System

Chronic recurrent multifocal osteomyelitis (CRMO)

CRMO...  

Churg-Strauss syndrome (CSS) or Eosinophilic granulomatosis (EGPA)

CSS...  

Cicatricial pemphigoid

CP...  

Cogan’s syndrome

CS...  

Cold agglutinin disease

Cad...  

Complex regional pain syndrome - CRPS (formerly known as reflex sympathetic dystrophy)

CRPS...  

Congenital heart block

Chb...  

Coxsackie myocarditis

Cm...  

Autoimmune Diseases - C, D

CREST syndrome

CREST syndrome - an acronym for: 


Calcinosis

Raynaud’s phenomenon

Esophageal dysfunction

Sclerodactyly

Telangiectasia

Crohn’s disease

Where: Digestive System

Cronkhite-Canada Syndrome (CCS)

CCS...

Cryptogenic organizing pneumonia (COP)

COP...

Dermatitis herpetiformis

DH...

Dermatomyositis

Where: Skin and Blood Vessels


Devic’s disease (neuromyelitis optica)

Dd...

Discoid lupus

Dl...

Dressler’s syndrome

Ds...

Autoimmune Diseases - E, F

Eczema/Atopic Dermatitis

Ecz...

Endometriosis

En...

Eosinophilic Esophagitis (EoE)/Eosinophilic gastroenteritis

Eos...

Eosinophilic fasciitis

Ef...

Erythema nodosum

En...

Essential mixed cryoglobulinemia

Emc...

Evans syndrome

Es...

Fibromyalgia

Es...

Fibrosing alveolitis/Idiopathic pulmonary fibrosis (IPF)

Es...

Autoimmune Diseases - G

Giant cell arteritis/temporal arteritis/Horton's disease

Gca...

Giant cell myocarditis

Gcm...

Glomerulonephritis

G...

Goodpasture’s syndrome/Anti-GBM/anti-TBM disease

Gs...

Granulomatosis with polyangiitis (GPA)/Wegener's granulomatosis

GPA...

Graves’ disease

Where: Endocrine System

Guillain-Barrè Syndrome (GBS)

Where: Nervous System

Autoimmune Diseases - H

Hashimoto’s Thyroiditis/autoimmune thyroiditis

Where: Endocrine System

Hemolytic anemia

Ha...

Henoch-Schonlein purpura (HSP)

HSP...

Herpes gestationis or pemphigoid gestationis (PG)

Hg...

Hidradenitis suppurativa (HS) (Acne inversa)

Hs...

Hurst’s disease/Acute hemorrhagic leukoencephalitis (AHLE)

Hd...

Hypogammaglobulinemia

Hypog...

Autoimmune Diseases - I, J, K

IgA nephropathy/Berger’s disease

IgA n

IgG4-related sclerosing disease (ISD)

IgG4...

Immune thrombocytopenia (ITP)/Autoimmune thrombocytopenia purpura

ITP...

Immune-mediated necrotizing myopathy (IMNM)

IMNM...

Inclusion Body Myositis (IBM)

IBM...

Interstitial cystitis (IC)

IC...

Juvenile diabetes (Type 1 diabetes)

IC...

Juvenile idiopathic arthritis (JIA)/Adult-onset still's disease

IC...

Juvenile myositis (JM)

IC...

Kawasaki disease

Kawasaki disease, also known as mucocutaneous lymph node syndrome, primarily affects children and is characterized by inflammation of medium-sized arteries throughout the body, particularly the coronary arteries, which can lead to heart complications. 


The condition also impacts the lymph nodes, skin, and mucous membranes of the nose, mouth, and throat. 

Autoimmune Diseases - L

Lambert-Eaton myasthenic syndrome (LEMS)

LEMS...

Leukocytoclastic vasculitis

Lv...

Lichen Planus (or Lichen Planopilaris/Follicular Lichen Planus)

Lp...

Lichen sclerosus

Ls...

Ligneous conjunctivitis

Lc..

Linear IgA disease (LAD)

Lad...

Lupus

Where: Joints and Muscles


Systemic Lupus Erythematosus (SLE) is the most serious. SLE can affect almost any organ or system in the body, including blood vessels, muscles, joints, the digestive tract, lungs, kidneys, heart and central nervous system.

             

SLE can also cause Lupus Nephritis (LN).


Discoid lupus causes a raised, scaly, red rash, usually on the face, scalp and neck and may cause scarring.


Drug-induced lupus is a type of lupus which is caused by prescription medications. Symptoms are similar to those of SLE; and once the medication is stopped, the symptoms usually cease.


Neonatal lupus is a rare disease that can affect some newborn babies of women with SLE or certain other immune system disorders. These babies may have a heart defect, skin rash, low blood count, and/or liver problems. However, most infants of mothers with SLE are born healthy.


Emotional Contributing Factors: 


Lee, L. S., et al. (2018) explored how stress and trauma contribute to depression in lupus patients. 

It found that individuals with lupus who had a history of trauma, including physical, emotional, or sexual abuse, were more likely to experience depressive symptoms. 


Depression, in turn, negatively affected the management of lupus, creating a vicious cycle of increased disease activity and poor mental health.


Reference (1): Lee, L. S., et al. (2018). The interplay of stress, trauma, and depression in systemic lupus erythematosus (SLE). Journal of Clinical Rheumatology, 24(2), 75-82. 


Bromberg, J. S., & Williams, M. R. (2016) examined the relationship between stress levels and quality of life in lupus patients. It found that higher stress levels were associated with lower quality of life, increased pain, and greater difficulty in managing the disease. 


The study also highlighted that lupus patients who had experienced significant trauma reported more severe symptoms and greater distress.

Reference (2): Bromberg, J. S., & Williams, M. R. (2016). Stress and quality of life in lupus: A cross-sectional study. Lupus, 25(12), 1293-1300. 


Lasselin, J., et al. (2015) found a strong association between early life trauma (such as abuse or neglect) and the development of autoimmune diseases, including lupus. 


The stress response caused by childhood trauma was linked to immune system dysregulation, which may increase the risk of developing autoimmune conditions. 


Reference (3): Lasselin, J., et al. (2015). Psychosocial stress, immune dysregulation, and disease activity in lupus: A pathophysiologic mechanism. Autoimmunity Reviews, 14(11), 1055-1062. 

Lyme disease

Ld...

Lymphocytic colitis/microscopic colitis

111

Autoimmune Diseases - M

Ménière’s disease

Md...

Microscopic polyangiitis (MPA)/ANCA-associated vasculitis

Mpa...

Mixed Connective Tissue Disease (MCTD)

MCTD...

Mooren’s ulcer

111

Mucha-Habermann disease or PLEVA (pityriasis lichenoides et varioliformisacuta)

Muc...

Mucous membrane pemphigoid (MMP) or ocular cicatricial pemphigoid (OCP)

MMP...

Multifocal Motor Neuropathy (MMN)

MMN...

Multiple sclerosis

Where: Nervous System

Myalgic encephalomyelitis/Chronic fatigue syndrome (ME/CFS)

Where: Systemic (including neurological, immune, digestive, cardiac and energy metabolism / energy production) 


Myalgic encephalomyelitis (ME), also known as Chronic fatigue syndrome (CFS), is characterised by overwhelming tiredness, that is not improved by rest. 


Those with the condition suffer from fatigue - that is so severe - it inhibits them from performing daily activities. 


Cognitive and sleep issues are also common in ME/CFS patients. 


Due to its similar appearance to other illnesses, diagnosis is challenging. 


ME/CFS is chronic and sometimes unpredictable, with symptoms and severity fluctuating over time. 


Emotional Contributing Factors - Research


Reference (1):  NEM, S-H., Hayes, LD., Mclaughlin, M., Berry, ECJ., and Sculthorpe, NF. (2025)    Post-traumatic Stress Disorder in People with Long COVID, ME/CFS, and Controls. 

The American Journal of Medicine. 2025; Apr;138(4):742-749. 


Reference (2):  Fennell, P.A., Dorr, N. and George, S.S. (2021). Elements of Suffering in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: The Experience of Loss, Grief, Stigma, and Trauma in the Severely and Very Severely Affected. Healthcare (Basel, Switzerland). Healthcare (Basel, Switzerland). 2021 May 9;9(5):553. 


Reference (3):  Krzeczkowska, A., Karatzias, T. and Dickson, A. (2015). Pain in people with chronic fatigue syndrome/myalgic encephalomyelitis: the role of traumatic stress and coping strategies. Psychology, health and medicine. 2015;20(2):210-6.    


Myasthenia gravis

Where: Nervous System

Myelin Oligodendrocyte Glycoprotein (MOG) Antibody Disease

MOG...

Myositis

Where: Joints and Muscles

Autoimmune Diseases - N, O

Narcolepsy

Narcolepsy is a chronic neurological disorder that disrupts the brain’s ability to regulate sleep-wake cycles and increasing evidence suggests that narcolepsy, ie. NT1 is an autoimmune disease. 


It is characterised by excessive daytime sleepiness and sudden sleep attacks.


The condition is divided in two types: 

  • Narcolepsy Type 1 (NT1) – Associated with cataplexy (sudden loss of muscle tone).
  • Narcolepsy Type 2 (NT2) – Does not include cataplexy.

Neonatal Lupus

Neonatal lupus is an uncommon autoimmune disease manifested primarily by cutaneous lupus lesions and/or congenital heart block. 


Maternal autoantibodies of the Ro/La family are present in virtually every case, although only approximately 1% of women who have these autoantibodies will have a baby with neonatal lupus. 


The cutaneous lesions of neonatal lupus may be present at birth, but more often develop within the first few weeks of life. Lesions are most common on the face and scalp, often in a distinctive periorbital distribution. Lesions tend to resolve in a few weeks or months without scarring. 


Source: https://pubmed.ncbi.nlm.nih.gov/15035648/

Neuromyelitis optica / Devic disease

No...

Neutropenia

Neutropenia is an abnormally low number of white blood cells. These cells, which are called neutrophils, help the body fight infection. 


White blood cells are produced in the bone marrow. They are released into the bloodstream, and travel wherever they are needed. 


Low levels of neutrophils occur when the bone marrow cannot replace them as fast as needed. A very severe infection may cause neutrophils to be used up quickly, and may also prevent the bone marrow from producing more neutrophils. 


In rare cases, mothers may have antibodies against their baby’s neutrophils. These antibodies cross the placenta before birth and cause the baby’s cells to break down (autoimmune neutropenia). 


In other rare cases, a problem with the baby’s bone marrow may lead to decreased white blood cell production. In many cases, neutropenia goes away on its own as the bone marrow recovers and begins to produce enough white blood cells. 

Ocular cicatricial pemphigoid

OCP...

Optic Neuritis

ON...

Optic Neuritis #2

ON2...

Autoimmune Diseases - P

Palindromic rheumatism (PR)

Pr...

Palmoplantar pustulosis (PPP)

PPP..

PANDAS (Pediatric autoimmune neuropsychiatric disorders associated with streptococcus infections)

PANDAS...

Paraneoplastic cerebellar degeneration (PCD)

PCD...

Paraneoplastic pemphigus

Pp...

Paroxysmal nocturnal hemoglobinuria (PNH)

PNH...

Parry-Romberg syndrome (PRS)/Hemifacial atrophy (HFA)/Progressive facial hemiatrophy

PRS...

Parsonage-Turner syndrome

P-T...

Pars planitis (peripheral uveitis)

Pp...

Pemphigoid gestationis (PG)

PG...

Pemphigus foliaceus

PF...

Pemphigus vulgaris

PV...

Autoimmune Diseases - P

Peripheral neuropathy

Pn..

Perivenous encephalomyelitis


Source:  https://rarediseases.info.nih.gov/diseases/11979/autoimmune-encephalitis 

Pernicious anemia (PA)

PA...

Pityriasis Lichenoides et Varioliformis Acuta / Mucha-Habermann disease (PLEVA)

PLEVA...

POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, skin changes)

POEMS stands for these signs and symptoms:


Polyneuropathy. Numbness, tingling and weakness in your legs — and over time, maybe in your hands — and difficulty breathing


Organomegaly. Enlarged spleen, liver or lymph nodes


Endocrinopathy. Abnormal hormone levels that can result in underactive thyroid (hypothyroidism), diabetes, sexual problems, fatigue, swelling in your limbs, and problems with metabolism and other essential functions


Monoclonal plasma-proliferative disorder. Abnormal bone marrow cells (plasma cells) that produce a protein (monoclonal protein) that can be found in the bloodstream


Skin changes. More color than normal on your skin, possibly thicker skin and increased facial or leg hair


Source:  https://rarediseases.info.nih.gov/diseases/7411/poems-syndrome 

Polyarteritis nodosa (PAN)

PAN...

Polyglandular syndromes type I, II, III (PDS)

PDS...

Polymyalgia rheumatica

P-T...

Polymyositis

Pp...

Postpericardiotomy syndrome

PG...

Primary biliary cirrhosis (PBC)/Primary biliary cholangitis

PF...

Primary sclerosing cholangitis (PSC)

PV...

Autoimmune Diseases - P, R

Progesterone dermatitis

Progesterone dermatitis is a rare condition characterized by a cyclic skin rash which develops premenstrually in women. 


The condition usually occurs in adulthood after the start of periods (menarche), and rarely during pregnancy or postmenopause. 


Signs and symptoms vary among affected individuals; skin findings that have been reported include hives, erythema multiforme, papulovesicles (an eczema-like rash), annular erythema, angiodema, mouth erosions and pruritus (itching). 

Progressive hemifacial atrophy (PHA) Parry Romberg syndrome

Parry Romberg syndrome is a rare disorder characterized by slowly progressive deterioration (atrophy) of the skin and soft tissues of half of the face (hemifacial atrophy), usually the left side. An autoimmune mechanism is suspected, and the syndrome may be a variant of localized scleroderma. It is more common in females than in males. Initial facial changes usually involve the tissues above the upper jaw (maxilla) or between the nose and the upper corner of the lip (nasolabial fold) and subsequently progress to the angle of the mouth, areas around the eye, the brow, the ear, and the neck.  


Source: https://rarediseases.info.nih.gov/diseases/7338/progressive-hemifacial-atrophy 

Psoriasis

Where: Skin and Blood Vessels


Psoriasis is a skin disease that causes itchy or sore patches of thick, red skin with silvery scales. 


One usually gets the patches on their elbows, knees, scalp, back, face, palms and feet, but they can show up on other parts of your body. Some people who have psoriasis also get a form of arthritis called psoriatic arthritis. 


A problem with your immune system causes psoriasis.  

Psoriatic arthritis

Where: Skin and Blood Vessels


Some people with psoriasis have psoriatic arthritis. It causes pain, stiffness, and swelling of the joints. It is often mild, but can sometimes be serious and affect many joints. 


The joint and skin problems don’t always happen at the same time. 


Causes:  


Psoriatic arthritis occurs when your body's immune system attacks healthy cells and tissue. 


The immune response causes inflammation in your joints as well as overproduction of skin cells.

It seems likely that both genetic and environmental factors play a role in this immune system response. 


Many people with psoriatic arthritis have a family history of either psoriasis or psoriatic arthritis. Researchers have discovered certain genetic markers that appear to be associated with psoriatic arthritis.


Physical trauma or something in the environment — such as a viral or bacterial infection — might trigger psoriatic arthritis in people with an inherited tendency.


Source: Mayo Foundation for Medical Education and Research (MFMER) 

Pulmonary Alveolar Proteinosis (PAP)

Pulmonary alveolar proteinosis, commonly known as PAP, is a rare lung syndrome that occurs in about 7 people per million in the general population, affecting both men and women of all ethnicities, regardless of socioeconomic class. 


Although primarily affecting people 30 to 50 years old, PAP can occur at any age. 


In PAP, there is the buildup of surfactant in the air sacs of the lungs (alveoli) that leads to problems getting oxygen into the body. Surfactant, a naturally produced fluid in the lungs, is normally present in the lungs at a certain level, yet if extra surfactant is not cleared properly, it can build up and cause difficulty breathing and other respiratory issues.


The 3 main causes of PAP are autoimmune, congenital, and secondary. 


Over 90% of people with PAP have the autoimmune form. 


In the autoimmune form, an antibody is formed that limits normal protein function (or macrophage function). This antibody is called granulocyte-macrophage colonystimulating factor (GM-CSF). 


The GM-CSF antibody prevents the growth of cells called macrophages, which are responsible for removing the extra surfactant from the air sacs in the lungs. The surfactant builds up and hinders oxygen getting in and carbon dioxide getting out of the body through the air sacs.


Source: American Thoracic Society - https://site.thoracic.org/  

Pure red cell aplasia (PRCA)

Pure red cell aplasia (PRCA) is an uncommon disorder in which maturation (growth) arrest occurs in the formation of erythrocytes (red blood cells). 


Secondary PRCA occurs in patients with conditions such as autoimmune disorders, thymomas, systemic lupus erythematosus, hematologic malignancies, and solid tumors. 

Pyoderma gangrenosum

Pyoderma gangrenosum is an uncommon, ulcerative cutaneous condition of uncertain etiology (cause). It is associated with systemic autoimmune related diseases in at least 50% of patients who are affected. The diagnosis is made by excluding other causes of similar-appearing cutaneous ulcerations, including infection, malignancy, vasculitis, collagen vascular diseases, diabetes, and trauma. 

Raynaud’s Syndrome

Narrowing of arteries that carry blood from the heart to other parts of the body, known as vasospasm attacks, results in reduced blood flow in the fingers and toes and is typically triggered by cold temperatures and emotional stress. 

Reactive arthritis/Reiter’s syndrome

Formerly referred to as Reiter’s syndrome, reactive arthritis causes inflammation in various joints in the body, especially the knees, feet, toes, hips and ankles. 


It typically develops following an infection (particularly sexually transmitted) or food poisoning. 


It is a form of autoimmune arthritis or joint inflammation, that occurs as a “reaction” to an infection elsewhere in the body. Besides this joint inflammation, reactive arthritis is associated with two other symptoms: redness and inflammation of the eyes (conjunctivitis) and inflammation of the urinary tract (urethritis). 


These symptoms may occur alone, together, or not at all. 

Relapsing polychondritis (RP)

Relapsing polychondritis is a rare disease in which cartilage in many areas of the body becomes inflamed. 


The disease most commonly affects the ears, nose and the airways of the lungs. 


The cause is not known, and it occurs most often in people in their 50s or 60s. 


One theory is that polychondritis might be an autoimmune disease, in which the immune system attacks the body rather than foreign invaders such as viruses. In polychondritis, it’s possible that a triggering event, perhaps an infection, sets off a reaction by the immune system, which unleashes an attack on the body’s cartilage. 


Some people may have a genetic makeup that makes them more prone to this. The disease does not seem to run in families. It sometimes appears in people who have other disease, such as rheumatoid arthritis, vasculitis (inflammation of blood vessels) and systemic lupus erythematosus (SLE or lupus). 


Source:  https://rarediseases.info.nih.gov/diseases/7417/relapsing-polychondritis 

Rheumatic Fever

Rheumatic fever is a disease that affects the heart, joints, brain, and skin and can cause permanent damage to the heart if left untreated.  


Although the causal link between strep throat/scarlet fever and rheumatic fever is still undetermined, rheumatic fever has been shown to develop following improperly treated strep throat and scarlet fever cases caused by group A streptococcus infections of the throat. 

Rheumatoid Arthritis (RA)

Where: Joints and Muscles (and Systemic)


Rheumatoid arthritis (RA) is a form of arthritis that causes pain, swelling, stiffness and loss of function in your joints. 


It can affect any joint but is common in the wrist and fingers. 


More women than men get rheumatoid arthritis. It often starts in middle age and is most common in older people. Children and young adults can also get it. 


One might have the disease for only a short time, or symptoms might come and go. 


The severe form can last a lifetime. 


Rheumatoid arthritis is different from osteoarthritis, the common arthritis that often comes with older age. 


RA can affect body parts besides joints, such as your eyes, mouth and lungs. 


RA is an autoimmune disease, which means the arthritis results from your immune system attacking your body’s own tissues. No one knows what causes rheumatoid arthritis. Genes, environment and hormones might contribute. Treatments include medicine, lifestyle changes and surgery. These can slow or stop joint damage and reduce pain and swelling. 


Emotional Contributing Factors - Research


John A. Sturgeon, Patrick H. Finan and Alex J. Zautra (2016) explained that chronic stress may activate the sympathetic nervous system and dysregulate the hypothalamic-pituitary-adrenal (HPA) axis, leading to increased inflammation. 


This heightened inflammatory response can exacerbate RA symptoms and potentially contribute to disease progression.


Reference (1): John A. Sturgeon, Patrick H. Finan and Alex J. Zautra (2016). Affective disturbance in rheumatoid arthritis: psychological and disease-related pathways. Nat Rev Rheumatology. 2016 

Jul 14;12(9):532–542. 


Carsten Spitzer, Stefanie Wegert, Jürgen Wollenhaupt, Katja Wingenfeld, Sven Barnow and Hans Joergen Grabe (2013) conducted a case-control study and found that women with a history of childhood trauma, including emotional abuse and neglect, had a higher risk of developing RA compared to those without such histories. 


The study suggests that early life stress may disrupt neuro-endocrine-immune networks, increasing RA susceptibility. 


Reference (2): Carsten Spitzer, Stefanie Wegert, Jürgen Wollenhaupt, Katja Wingenfeld, Sven Barnow and Hans Joergen Grabe (2013). Gender-specific association between childhood trauma and rheumatoid arthritis: A case-control study. Journal of Psychosomatic Research. 2013. Volume 74, Issue 4: 296-300.


M A Lumley, J E Kelley and J C Leisen (1997) also found that how individuals process and express emotions can influence RA outcomes. 


For instance, increased expression of negative emotions and frequent thoughts about stressful events were associated with greater pain and physical dysfunction in RA patients. 


Reference (3): M A Lumley, J E Kelley and J C Leisen (1997). Health effects of emotional disclosure in rheumatoid arthritis patients. Journal of Health Psychology. 1997.  Apr;2(2):255-64.


Autoimmune Diseases - S

Sarcoidosis

Characterised by the growth of granulomas, which are abnormal accumulations of inflammatory immune system cells called macrophages. 


Granulomas can appear in various parts of the body but are typically found in the lungs and lymph nodes. 

Schmidt syndrome or Autoimmune polyendocrine syndrome type II

Schmidt syndrome also known as Polyglandular autoimmune syndrome type 2 is a rare autoimmune syndrome that commonly has the constellation of 3 diseases: 

diabetes mellitus type 1, hypothyroidism and adrenal insufficiency.  

Scleritis

Scleritis is an inflammation of the sclera (the white outer wall of the eye). 


Inflammation of the sclera is often linked to autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus. 


Sometimes the cause is unknown. 


Scleritis occurs most often in people between the ages of 30 and 60. 


It is rare in children. 

Scleroderma

Where: Skin and Blood Vessels


An overproduction of collagen protein which leads to the hardening and inflammation of connective tissues and skin. 


Scleroderma can be localized, meaning it only affects the skin, or it can be systemic, meaning it affects other parts of the body as well (such as the heart, lungs, kidneys, and digestive tract). 

Sjögren's Syndrome

Where: Skin and Blood Vessels


Along with symptoms of extensive dryness, other serious complications include profound fatigue, chronic pain, major organ involvement, neuropathies, and lymphomas.


As a systemic disease, affecting the entire body, symptoms may remain steady or worsen overtime. There is no one single progression of the disease and this can make it challenging for patients and their physicians. 


While some people experience mild discomfort, others suffer debilitating symptoms that greatly impair their functioning. 


Early diagnosis and proper treatments are important as they may prevent serious complications and greatly improve a patient’s quality of life.


About half of the time Sjögren’s occurs alone, and the other half it occurs in the presence of another autoimmune connective tissue disease such as Rheumatoid Arthritis, Lupus, or Scleroderma.


In addition, Sjögren’s is often misrepresented as a rare disease, however it is estimated that there are four million Americans living with this disease, making it one of the most prevalent autoimmune diseases.


Source: Sjögren's Foundation

Small fiber sensory neuropathy (SFSN)

SFSN affects the small fibers of the peripheral nervous system, resulting in sensory disturbances which affect different areas of the body. 


The 2 types of SFSN are length-dependent SFSN, and non-length-dependent SFSN and these differ based on the location of the symptoms. 

Stiff person syndrome (SPS)

Stiff person syndrome (SPS) is a rare disease of the nervous system. 


Progressively severe muscle stiffness typically develops in the spine and lower extremities; often beginning very subtly during a period of emotional stress. 


Most patients experience painful episodic muscle spasms that are triggered by sudden stimuli. 


An autoimmune component is typical and patients often have other autoimmune disorders.  

Susac’s syndrome

Susac's syndrome is a very rare autoimmune condition that affects the very small blood vessels in the brain, retina, and inner ear (cochlea). 


The condition is characterized by three main symptoms: brain disease (encephalopathy), hearing loss, and vision loss. 


Some people may not have all signs of Susac syndrome, but instead develop only specific combinations of the symptoms. 


Susac syndrome affects women more than men. The age at which symptoms begin is usually between 20 and 40 years, but some people have symptoms earlier or later than this age range.


Source: https://rarediseases.info.nih.gov/diseases/7713/susac-syndrome  

Sydenham’s chorea

Characterised by rapid, jerky, irregular, and involuntary movements (especially of the face and limbs). 


In children, these symptoms often appear after strep throat or rheumatic fever, caused by a group A streptococcus infection. 


Group A streptococcus bacteria can react with a part of the brain called the basal ganglia to cause Sydenham’s chorea. 

Sympathetic ophthalmia (SO)

Sympathetic ophthalmia (SO) is a bilateral diffuse granulomatous uveitis (a kind of inflammation) of both eyes following trauma to one eye. It can leave the patient completely blind. 


Symptoms may develop from days to several years after a penetrating eye injury. 


Source: Arevalo, J Fernando et al. “Update on sympathetic ophthalmia.” Middle East African journal of ophthalmology vol. 19,1 (2012): 13-21. doi:10.4103/0974-9233.92111 

Systemic Lupus Erythematosus (SLE)

SLE is the most common form of lupus in which the immune system attacks its own healthy tissues resulting in widespread inflammation and tissue damage of joints, skin, brain, lungs, kidneys, and blood vessels. 

Autoimmune Diseases - T

Takayasu’s arteritis

TA... 

Testicular Autoimmunity Overview

TAO...

Thyroid eye disease / Graves’ ophthalmopathy / thyroid-associated orbitopathy

TED... 

Temporal arteritis/giant cell arteritis

TA...


Thrombocytopenic purpura (TTP)/Thrombotic thrombocytopenic purpura (Ttp)

Ttp...

Thyroid Eye Disease (TED)

TED...

Tolosa-Hunt syndrome (THS)

THS...

Transverse myelitis

Tm...

Type 1 Diabetes/insulin-dependent diabetes

Where: Endocrine System

Autoimmune Diseases - U, V, W

Ulcerative Colitis (UC)

Where: Digestive System


Ulcerative colitis (UC) is an autoimmune related disease that causes inflammation and sores, that forms ulcers and inflammation, in the innermost lining of the rectum and colon (of the digestive tract). It is one of a group of diseases called inflammatory bowel disease. 


4 types of Ulcerative Colitis, based on the location of the body:


1. Ulcerative Proctitis: affects the rectum on the area, closest to the anus

2. Proctosigmoiditis: rectum and the sigmoid colon — the lower end of the colon 

3. Left-sided colitis: affects the rectum up through the sigmoid and descending colon

4. Pancolitis: affects the entire colon 

Undifferentiated Connective Tissue Disease (UCTD)

Undifferentiated connective tissue disease (UCTD) is a systemic autoimmune disease. 


UCTD occurs when the body’s natural immune system does not behave normally. 


It is also when the symptoms and lab test results of a systemic connective tissue disease are present, however do not meet enough characteristics for a specific diagnosis (such as rheumatoid arthritis or lupus). 


Instead of serving to fight infections, such as bacteria and viruses, the body’s own immune system attacks itself. 


In UCTD, autoimmunity may cause the immune system to attack specific parts of the body resulting in a variety of problems. The phrase “connective tissue disease” is used to describe the diseases of the immune system.


These represent systemic autoimmune diseases that often involve the joints, cartilage, muscles, and skin. They can also involve any other organ system, such as the eyes, heart, lungs, kidneys, gastrointestinal tract, bone marrow, nervous system and blood vessels. 


Examples of connective tissue diseases include lupus, scleroderma, rheumatoid arthritis, Sjögren’s syndrome, myositis and vasculitis. 

Uveitis

Uveitis is swelling and irritation of the uvea, the middle layer of the eye. 

The uvea provides most of the blood supply to the retina. 


Uveitis can be caused by autoimmune disorders, including rheumatoid or ankylosing spondylitis. It can also be caused by infection or exposure to toxins. 


The most common form is anterior uveitis. This involves inflammation in the front part of the eye. It is often called iritis, because it usually only affects the iris, the colored part of the eye. 


The disorder may affect only one eye and the inflammation may be linked with autoimmune diseases, however most cases involve healthy people.  

Vasculitis

Where: Skin and Blood Vessels


Vasculitis is an autoimmune related inflammation of the blood vessels. 


It happens when the body’s immune system attacks the blood vessel by mistake. It can happen because of an infection, a medicine, or another disease. 


Vasculitis can affect arteries, veins and capillaries. 


Arteries are vessels that carry blood from the heart to the body’s organs. Veins are the vessels that carry blood back to the heart. Capillaries are tiny blood vessels that connect the small arteries and veins. 


When a blood vessel becomes inflamed, it can narrow, making it more difficult for blood to get through, close off completely so that blood can’t get through, or stretch and weaken so much that it bulges. 


The bulge is called an aneurysm. If it bursts, it can cause dangerous bleeding inside the body. 


The main goal of treatment is to stop the inflammation.

Vitiligo

Where: Skin and Blood Vessels


Vitiligo causes white patches on your skin. It can also affect your eyes, mouth and nose. 


A skin disease that occurs when autoantibodies attack melanocytes (the skin cells that produce melanin or the chemical that produces skin color). There are two main types of vitiligo: non-segmental (symmetrical white patches on both sides of the body) and segmental (affects just one area of the body). 


Vitiligo is found in several subtypes, by the parts of the body, where discoloration occurs: 


A. Universal:  widespread pigment loss across the body


B. Generalised: scattered skin patches around the body 


C. Localised: skin patches found on limited areas of the body 


D. Mucosal: affects the mucous membranes found in the mouth and/or genitals 


E. Trichrome: instead of a smooth white depigmented patch, skin patches contain a white mixed with lighter hypopigmented patches 


It occurs when the cells that give your skin its color are destroyed. 


It is more common in people with autoimmune diseases and it might run in families. 

Vogt-Koyanagi-Harada disease

Vogt-Koyanagi-Harada disease is a rare disorder of unknown origin that affects many body systems, including as the eyes, ears, skin, and the covering of the brain and spinal cord (the meninges). 


The most noticeable symptom is a rapid loss of vision. There may also be neurological signs such as severe headache, vertigo, nausea, and drowsiness. 


Loss of hearing, and loss of hair (alopecia) and skin color may occur along, with whitening (loss of pigmentation) of the hair and eyelashes (poliosis). 


Source: https://rarediseases.org/rare-diseases/vogt-koyanagi-harada-disease/

Warm autoimmune hemolytic anemia

Warm antibody hemolytic anemia is the most common form of autoimmune hemolytic anemia. 


It is defined by the presence of autoantibodies that attach to and destroy red blood cells at temperatures equal to or greater than normal body temperature.


The disease is characterized by symptoms related to anemia, including fatigue, difficulty breathing, jaundice and dark urine. 


In severe disease, fever, chest pain, syncope or heart failure may occur. 


Hemolysis (the breakdown of red blood cells) occurs mainly in the spleen and mild splenomegaly is relatively common.   


Source: https://rarediseases.info.nih.gov/diseases/7876/warm-antibody-autoimmune-hemolytic-anemia 

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