OSTEOARTHRITIS (OA)
Osteoarthritis is the most common form of arthritis,
affecting around 5-10% of the total population, particularly women.
It develops when articular cartilage (the smooth covering over bones
in the joints) starts to break down, usually as a result of trauma,
ageing or failure of joint repair and maintenance mechanisms. Degradation
of the cartilage can be associated with underlying bone damage,
thickening and bone-on-bone friction.
Symptoms include stiffness, pain and tenderness in the joints
and surrounding muscles and ligaments, possibly with fatigue, reduction
in motor skills, and deformities. The most common pattern of joint
involvement in OA involves the major weight-bearing joints such
as the hips, knees or lower spine, with neck and hands also being
frequently affected sites.
There is no single cause for OA, with identified risk factors including:
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Being overweight
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Advancing age
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Low socio-economic status
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Hereditary factors
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Chronic stress across joints or joint trauma
(such as in sports injuries)
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Other metabolic or inflammatory disorders
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Because of the gender differences in incidence, hormones (especially
oestrogen) are suspected to have a relationship to OA, but there
is conflicting evidence.
Osteoporosis-not arthritis
Osteoporosis is a non-arthritic disorder, not to be confused with
OA. It is a condition in which the bones lose calcium, become fragile
and tend to break more easily, and usually affects people over 40,
mostly women as hormonal changes accompanying menopause accelerate
the loss of calcium.
RHEUMATOID ARTHRITIS (RA)
Rheumatoid arthritis affects around 2-3% of the population, again
with greater incidence in women. It is a progressive disease, with
onset most likely between 25-50 at a time when people are active
in the workplace or family care roles. RA is characterised by inflammation
within joints that serves no evidently useful purpose and which
damages joint structures. The synovial membrane that lines joints
is thickened and an over-production of synovial (joint) fluid occurs.
SYMPTOMS: The joints become painful, swollen, stiff and,
as the process continues, deformed from damage to the cartilage
and other soft tissue. Other symptoms include:
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Fatigue
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Interrupted sleep
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Weight loss
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Anaemia
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Nodules (in 30% of people)
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Ulcers
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Atrophic skin
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Muscle weakness
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Impaired joint function
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Inflammation of the heart, lungs, eyes, nerves,
blood vessels and lymph glands
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There is significant morbidity and mortality (over half of patients
will have to reduce significantly or stop work after ten years of
the disease). Like OA, RA is multifactorial in origin (genetic,
hormonal, environmental and other factors). Family history is a
key risk factor. Hormonal influences are evident with pregnancy
associated remissions, a lifelong protective effect of pregnancy,
and never having children conferring risk. Other possible contributing
factors include race, diet, trauma, and 'triggering agents' (most
likely bacteria or virus). Climatic conditions can exacerbate discomfort.
FIBROMYALGIA
Fibromyalgia (previously known as fibrositis) is a condition in
which discomfort is widespread and felt within the muscles and ligaments,
which may be tender. Damage to joints or other tissues is not a
feature. A common association with sleep dysfunction and irritable
bowel symptoms suggests an underlying neural irritability. Fatigue,
feelings of demoralisation and seemingly insoluble life stresses
may be part of the picture.
Fibromyalgia is to be distinguished from 'soft tissue rheumatism'
which refers to irritation or inflammation of structures such as
ligaments and the synovial sacs (bursae) that lubricate tendon movement.
SYSTEMIC LUPUS ERYTHEMATOSUS: Systemic Lupus Erythematosus
(usually abbreviated to lupus or SLE) is a chronic inflammatory
autoimmune disease of the connective tissues. It affects the skin,
especially in sun exposed areas such as the cheeks, which become
red and scaly and various internal organs (kidneys, heart, lungs
and brain can all be affected by inflammation and subsequent scar
tissue). Lupus often causes:
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General fatigue
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Tiredness
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Loss of concentration and memory
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Internal organ involvement can lead to organ failure and death.
GOUT
Gout is caused by the reaction of defence cells in joints to the
presence of uric acid crystals. Uric acid (a.k.a. urate) is a by-product
of the breakdown of the purines in the body. (Purines are components
of the genetic template (DNA) and of certain messenger substances
within cells.) Gout is characterised by severe acute attacks of
joint pain and swelling, which typically affect joints such as the
big toe, the ankle, knee and elbow. An excess of urates can also
cause kidney damage, including the formation of stones.
ROSS RIVER VIRUS
The mosquito-transmitted Ross River virus and the similar Barmah
Forest virus cause epidemic polyarthritis-acute arthritis in many
joints causing severe aches and pain. Viral arthritis does not usually
damage the joints like RA, but the arthritis and fatigue can sometimes
last for years before the joint returns to normal. Symptoms include
chronic fatigue, rashes, severe headaches, impaired concentration
and memory as well as depression. There is no specific treatment
or vaccination, although scientists are working to develop a vaccine.
JUVENILLE ARTHRITIS (JA)
Juvenile Arthritis can resemble adult RA but other distinctive patterns also occur. With one in 1,000 Australian children having Juvenile Arthritis it is one of the most prevalent and chronic illnesses among children. It has a higher prevalence than juvenile diabetes or cerebral palsy but often, because the symptoms are dismissed as "growing pains", Juvenile Arthritis goes untreated during the early stages of the disease. While some patients go into remission, others battle the symptoms lifelong.
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