The presentation of the disease varies considerably from one patient to another.^[7]

Generally, the symptoms include nonspecific symptoms common to connective tissue diseases such as

• fatigue. This is common in autoimmune diseases, and is the patient's primary concern.^[8]
• malaise and
• fever.^[9]

These can be the initial presentation for some patients.^[3]

Other symptoms associated with UCTD include :^[10]

• joint pain - the most common symptom occurring in up to 86% of patients.^[3] The pain is often an aching or arthritis-like pain in the elbows, wrists, hands, and knees, in a symmetrical pattern.^[11]
• dry eyes
• dry mouth
• hair loss
• joint inflammation
• mouth ulcers
• Raynaud's phenomenon
• sun-sensitive rash

Clinical presentation in some people diagnosed with UCTD may show :^[12]

• positive ANA test. Patients with UCTD usually have positive ANA.^[13]
• a decrease in the number of white blood cells
• anemia
• abnormal nerve sensations in the extremities
• inflammation of the lining of the heart and/or lungs
• a decrease in platelet count

Pulmonary involvement, such as nonspecific interstitial pneumonia, can be a complication of the disease.^[5]

UCTD is caused^{[citation needed]} by genetic and environmental factors. It may be triggered^{[citation needed]} by factors such as:

• Exposure to harmful products such as cigarette smoke.
• Exposure to an atmospheric pollutant, there are primaries air pollutants (nitrogen oxides (NOx), sulfur dioxide (SO2), volatile organic compounds (VOCs), hydrocarbons and certain metals (plomb, cadmium…)) or secondaries (created in the atmosphere through chemical reactions between pollutants).
• Exposure to UV light.

T-cell hypothesis edit

Populations of regulatory T cells are believed to be responsible^{[citation needed]} for the onset of the disease. When there is a decline of these cells, manifestations of diseases would begin to appear giving an idea of the vital role of these cells in the prevention of autoimmune diseases. Moreover, an additional decrease could unfortunately worsen the pathological state and lead to the differentiation of an undifferentiated connective tissue disease into a differentiated connective tissue disease with a poorer prognosis. Due to the wide range of variation in the inclusion criteria of the disease, up to 50% of patients diagnosed with connective tissue disease may have undifferentiated disease of the underlying connective tissue.

Diagnosis edit

There are no formal diagnostic criteria for UCTD. It is determined by a differential diagnosis. Diagnostic tests are undertaken to determine whether a patient has a disease assured or undifferentiated of the connective tissues.^[9]

Patients with UCTD usually have positive ANA (antinuclear antibody), and raised ESR (erythrocyte sedimentation rate) values, without typical autoantibody specificities.^[13] Some 20% of the general population,^[14] and up to 15% of completely healthy people,^[15] test positive for ANA, but nonetheless this is regarded by some as almost always a sign of an autoimmune disorder.^[11] If more specific types of ANAs or other proteins are present, other autoimmune conditions (not UCTD) are implied.^[11][16]

Other mechanisms that may be used^{[citation needed]} are tests for Anti-histone antibodies, Chromatin and vitamin D, and chest X-ray to show signs of pericardial effusion.^{[citation needed]}

Classification criteria edit

Patients may be included for UCTD research if they have:

• Signs and symptoms which (a) are suggestive of a connective tissue disease, but (b) do not meet the criteria of any defined connective tissue diseases,^[11] and (c) have lasted for at least three years. (Note if less than three years may be regarded as early UCTD).
• Positive ANA test on two different occasions.^[3][17]

UCTD is normally managed primarily as an outpatient. Meds can be used to manage aspects of the disease.^[3]

Treatment depends largely on the progression of the individual disease and the nature of the symptoms presented. The antimalarial medication, the corticosteroid and other medications may be prescribed, as the treating physician considers appropriate:^[18]

• Nonsteroidal anti-inflammatory drug against pain.
• corticosteroids stéroïdes anti-inflammatory (like naproxen).
• In severe cases, there is the possibility to use immunosuppressive drug.
• Antimalarial medication (like hydroxychloroquine) that can inhibit chemotaxis of neutrophil and eosinophil.
• Calcium channels blockers treatment relax smooth muscles and decrease the resistance of Peripheral vascular system. This can help in managing the Raynaud phenomenon.

Possible complications edit

Complications are present with an affected or injured system, such as the pulmonary system present a lesion and inflammation in the long term, an interstitial lung disease (in 88% of cases, severe interstitial lung disease) or a pulmonary fibrosis. If the heart is affected, a hypertrophy can occur, leading to a cardiomegaly.^[3] Organs can also be affected (neurological or renal manifestations) and life-threatening conditions can occur.

Affected pregnant women follow a careful clinical observation because they are more likely to see a progression of the disease. Those with the disease at the beginning of pregnancy will keep the disease undifferentiated against 25% who progress to a defined disease at the end of pregnancy. In addition, 45% of pregnancies with the disease end in preterm birth.

Deterrence and patients education edit

Early recognition and knowledge of the onset of UCTD can help patients manage and control their disease. Patients should be informed of common agents and triggers to help manage symptoms to shorten the duration of the disease and prevent complications.^{[citation needed]}

Improving health care team outcomes edit

Undifferentiated connective tissue disease occurs for various reasons, underlying factors may affect several organs depending on individual sensitivity. Coordination of care between primaries clinicians and experts (like rheumatologist) can help achieve optimal patient outcomes.^{[citation needed]}

Progression edit

30-40% of UCTD cases may develop into a defined connective tissue disease as more diagnostic criteria are progressively met.^[3] This generally happens within 5 years of onset.^[19]

Several factors may help predict progression:

• the presence of cytopenia at the time of the diagnostic.
• the degree of modification of the capillaroscopy test (skin blood vessel study technique) of nail fold during the follow-up.
• the presence of antinuclear antibodies.
• young age.^[20]
• severe vitamin D deficiency.^[21]
• the presence of autoantibodies anti-dsDNA, anti-Sm and anti-cardiolipin correlates with the development of systemic lupus erythematosus in particular.^[18]

The rate of progression is higher in the first five years following the onset of the disease and tends to decrease over time. Patients progressing to a defined disease seem to see a slight progression of the disease with a mitigated risk of developing complications.^[3]

Remaining undifferentiated edit

Most UCTD cases will remain undifferentiated. UCTD itself usually has a mild clinical course, particularly if there is low organ involvement. Most patients who remain undifferentiated tend to not experience major organ involvement.^[22]

Up to 10-20% of patients diagnosed with UCTD will never progress to a defined disease and their symptoms will decrease or disappear.^[3]

About 12% of patients will go into remission.^[23][22]

Particular studies edit

• In a Bulgarian study, after 5 years, 34% had developed into a defined connective tissue disease (with the highest probability of development being within the first two years after onset of symptoms), 54% continued undifferentiated and 12% were in remission.^[22]
• In a US study, after 10 years, 37% had developed into a defined connective tissue disease, 43% continued undifferentiated and 20% were in remission.^[22]
• In a Spanish study, after a mean follow-up of 11±3 years, 14% had developed a definite CTD, 62% continued undifferentiated, and 24% were in remission.^[24]
• In an Italian study (in which 58% had ANA abnormalities), after 5 years, 6% had developed a defined autoimmune disease. The remaining 94% saw clinical and serological features litte changed in the period and quite stable. 11% of these were and remained asymptomatic.^[25]

Up to 90% of UCTD cases are females between 32 and 44 years old.^[3][26] In the United States up to 78% of patients were female, against 93 to 95% in Italy and 94% in Hungary. Higher female prevalence is common in autoimmune diseases.^{[citation needed]}

In the United States, up to 72% of patients diagnosed with UCTD were white skinned.^[3]

Prevalence of UCTD has been estimated at 2 people per 100,000 people per year.^[27] Annual incidence has been estimated as varying from 41 to 149 per 100,000 adults.^[28][29][30] It has also been suggested that UCTD is a relatively common condition seen in rheumatology practice, making up 10-20% of referrals to tertiary care clinics.^[31]

Classical epidemiological data for UCTD are not available due to the limited literature exploring the disease. Also, differences in patient selection criteria in existing studies make comparisons between them difficult.^[1]

The term was first suggested in 1980,^[32] as connective tissue disease in patients whose features did not meet other classification criteria.^[3] In 1999 a study noted "In recent years there has been growing concern regarding the diagnosis of incomplete forms of the autoimmune diseases."^[25] and the first classification criteria were proposed in that year.^[1]

Historically the condition was sometimes called undifferentiated connective tissue syndrome, latent lupus or incomplete lupus.^[1]