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Chapter 1 Introduction to Pathophysiology; Cellular Responses to Stress, Injury, and Aging

Section 2 Diagnosis, Prognosis and Epidemiology

Zoë Soon

Diagnosis, Prognosis, Morbidity and Mortality

 

Diagnosis The identification of the disease, disorder, or syndrome.  An accurate diagnosis is essential for appropriate treatment and helps in making a prognosis.  An accurate diagnosis can depend on the availability of specific tests and medical equipment.
Prognosis The predicted outcome of an illness or injury.
Morbidity The rate of a particular disease within a population.
Mortality The typical death rate associated with a disease or disorder.
Etiology The study of the cause of a disease, disorder, or syndrome.

Etiology – Categories of Causes

The causes of diseases, disorders, and syndromes can be organized into the following categories:

  • Infectious diseases: caused by viruses, bacteria, fungi, helminths, and protozoa.
  • Immune dysfunction:  illness arising from a deficient or overactive immune system (e.g., allergies, autoimmune diseases).
  • Trauma:  bone fractures, wounds, injuries.
  • Nutritional deficiencies.
  • Cancer.
  • Lifestyle factors.
  • Toxins.
  • Genetics.
  • Congenital defects.

Genetic Disorders, Hereditary Diseases, and Congenital Defects

Three closely related but distinct terms deserve careful attention:

Genetic Disorder An ailment caused by a DNA mutation.  Mutations can be inherited or occur spontaneously during cell division.  Exposure to carcinogenic agent also damages DNA and give rise to cancer.  Cancer is therefore an example of a genetic disorder caused specifically by mutations in genes that control cell division (mitosis) and apoptosis.
Hereditary Disease A genetic disease that has been inherited from a parent (e.g., Hemophilia, resulting from a mutation in a clotting factor gene).
Congenital Defect Anatomical or functional defects occurring during embryonic or fetal development, presenting at birth.  The word comes from Latin con- (‘with’) + genesis (‘creation of’).

Examples of genetic disorders you may be familiar with:

  • Cystic fibrosis:  recessive, caused by a mutation on chromosome 7.
  • Sickle cell anemia: recessive, caused by a mutation in the hemoglobin beta chain gene on chromosome 11.
  • Marfan syndrome:  autosomal dominant, mutation on chromosome 15.
  • Huntington’s disease:  autosomal dominant, mutation on chromosome 4.
  • Down syndrome: inheritance of three copies of chromosome 21 (trisomy 21).
Sickle Cell Anemia
Sickle cell anemia is part of a group of genetic disorders known as sickle cell disease. In those with sickle cell anemia, red blood cells, which are usually round, flexible and flow easily within blood vessels, are sickle-shaped and lead to blockages to blood flow. This sickle shape is caused by an abnormal form of hemoglobin, a protein responsible for carrying oxygen. As a result, less oxygen is delivered to organs of the body, leading to severe consequences, including stroke.
Marfan syndrome
A positive wrist sign in a patient with Marfan syndrome, where the thumb and little finger overlap when grasping the wrist of the opposite hand. Marfan syndrome is a genetic disorder that affects connective tissues (gives support, protection, and structure to other tissues and organs), commonly affecting the heart, eyes, blood vessels and skeleton. Individuals with Marfan syndrome are typically tall and thin, with unusually long arms, legs, and digits.
Example of congenital multifactorial defect: down syndrome.
Karyotype (an individual’s complete set of chromosomes) of trisomy 21 (Down syndrome), where there is the presence of a third copy of chromosome 21.

The most common congenital defects include: congenital heart defects, hypospadias (slight misplacement of urethra within penis), clubfoot (inward turn of foot), cleft lip and cleft palate (incomplete fusion of right and left palatine and/or maxillae bones in the roof of the mouth), limb defects, and mental dysfunction.  Many of these can be surgically corrected or managed with physical therapy.

The causes of congenital defects are most often multifactorial – meaning many factors are responsible – including genetic susceptibilities, fetal exposure to teratogens.

What are Teratogens?

All agents that can cause congenital defects, miscarriages, or stillbirths are grouped together and called teratogens.  These include:  various microbes, alcohol, drugs, toxins (e.g., mercury, lead), gamma radiation, x-rays, and nutritional deficiencies.

A growing embryo and later fetus are especially susceptible during organogenesis (the formation of new organs), when teratogens can have the most harmful effects.  The severity of congenital defects typically depends on the timing, duration, and concentration of teratogen exposure, as well as the fetus’s genetic composition.

Examples include:  Fetal Alcohol Syndrome (caused by prenatal alcohol exposure), and congenital defects caused by infections such as rubella, measles, mumps, chlamydia, and syphilis – which can cause blindness, deafness, and cognitive delay.

Zika virus, spread by mosquito species in tropical regions (e.g., Uganda, Central America) has been linked to congenital defects including microcephaly, reduced brain development and cognitive impairments.

The overall risk factors for congenital defects also include maternal health, maternal age, and maternal exposure to cigarette smoke.

Mercury contamination is a problem in the Florida Everglades
Mercury contamination is a problem in the Florida Everglades, and in many bodies of water throughout the world (Photo by Tom Friedel). In the Everglades, mercury is supplied via atmospheric deposition, groundwater discharge, and stormwater run-off. Mercury content in the water and fish are so high that swimming or fish consumption should be limited or completely abstained to avoid mercury toxicity.
Cutaneous mercury granuloma is a rare disorder caused by the introduction of elemental mercury (Hg) into skin. treat an open wound.
Cutaneous mercury granuloma is a rare disorder caused by the introduction of elemental mercury (Hg) into skin (Photo by Y. Rosen). Metallic mercury in tissue appears as black, opaque, spherical globules of varying size. They provoke a granulomatous foreign-body reaction composed of foreign body giant cells, granulomas and a mixed inflammatory infiltrate. The method of introduction could be skin penetration by a mercury-containing object or the use of mercury-containing medication to treat an open wound.
United States Environmental Protection Agency (U.S. EPA) emergency response contractors clean up mercury at a Nevada home. Symptoms of mercury poisoning vary depending on exposure dose, duration, method, and type, though symptoms can include kidney and central nervous system damage, or death.
Example of congenital multifactorial defect: hypospadias.
Hypospadias is a congenital malformation in males, characterized by abnormal fetal development of penis so that the opening of the urethra is located on the underside of the penis rather than the tip. In subcoronal hypospadias, the urethral opening is located just below the head of the penis. In midshaft hypospadias, the urethral opening is located halfway down the underside of the penis. In penoscrotal hypospadias, the urethral opening is located where the shaft of the penis meets the scrotum.
Example of a congenital multifactorial defect: cleft lip and cleft palate.
Cleft lift and cleft palate are among the most common congenital defects, where parts of the upper lip or palate do not fuse properly in utero. Unilateral cleft lip and/or palates occur if the defect only occurs on one side, while Bilateral cleft lip and/or palates occur when the defect is on both sides.

 

Example of a congenital multifactorial defect: clubfoot
Clubfoot, which affects the muscles and bones in the feet, is the most common congenital malformation (occurs in about 0.1% of births). Affected feet (can be only one or both) twist down and rotate inwards.
A foot abduction brace consists of two straight-border, high-top, open-toe shoes attached to an aluminum bar, with the heels of the shoes at shoulder distance apart and the shoes themselves set at 60-70 degree angles. This device is used as part of the Ponseti method (a series of casting and orthotic brace treatments) of non-surgically treating young children born with clubfoot.

Clinical Manifestations – Signs and Symptoms

Clinical Manifestation A formal term for signs or symptoms
Sign Observable indicators of illness – fever, rash, lab test results, imaging results
Symptom Indicators of illness that are not observable by another person – pain, weakness, fatigue, nausea, headache, cramps, sleeplessness.

 

 

What is a Biopsy?

A biopsy refers to the excision or scraping of a tissue sample, usually examined under a microscope for signs of disease.  For example, a Pap smear involves scraping cervical cells and sending them to a lab where cellular morphology is examined for early signs of cervical cancer.  The Pap smear is typically recommended every 2-3 years (as per physician recommendation) after an individual becomes sexually active.  Early detection of cervical cancer greatly improves the chance of successful treatment.

Idiopathic and Iatrogenic Disease

Idiopathic A disease of unknown cause.  The prefix idios is Greek for ‘one’s own’.  The synonym essential is also used (e.g., essential hypertension:  high blood pressure not resulting from a medical condition, most often linked to obesity, unhealthy diet, sedentary behaviour and family history.
Iatrogenic A disease caused by the health care practitioner or by the treatment itself.  The prefix iatro is Greek for ‘doctor’.

 

Predisposing Factors (Risk Factors)

A predisposing factor is another term for risk factor – a condition or characteristic that increases a person’s susceptibility to developing a disease.  Common risk factors include:

  • Age:  Older age increases risk for cancer and many other diseases, as a lifetime of exposure to damaging agents accumulates and cells become less effective at providing protection, fighting infection and healing tissue.
  • Biological sex: Females are more susceptible to autoimmune diseases and lung cancer.  Males are more susceptible to cardiovascular disease, X-linked colour blindness, and Duchenne muscular dystrophy.
  • Genetics:  Certain genetic profiles increase susceptibility (e.g., sickle cell anemia, cystic fibrosis).
  • Congenital defects:  Some defects (e.g., congenital heart defects) can make organs less robust and more susceptible to wear and tear, injury and disease.
  • Diet:  Malnutrition impairs growth, cognitive function, and organ function globally.  In many Western countries, diets high in fat, sugar, and/or salt increase risk for heart disease, diabetes, and possibly Alzheimer’s disease.
  • Occupation:  Exposure to radiation, asbestos coal dust, and pollutants, increases risk for cancers and lung disease.  Pesticide use is being linked to the onset of Parkinson’s disease.
  • Location:  Geography determines exposure to local infectious microbes, sociodemographic factors, and cultural practices.  For example, malaria is endemic to tropical regions where the Plasmodium protozoan parasite is carried by specific mosquitoes.
Example of relapse
Electron micrograph of red blood cells infected with Plasmodium falciparum, the parasite that causes malaria in humans. Patients with malaria often exhibit a relapse of symptoms following a peak of symptoms and, occasionally, long periods of dormancy.

 

Neglected Tropical Diseases (NTDs)

Neglected Tropical Diseases (NTDs) are a group of diseases most prevalent in the tropics, that despite affecting millions of people each year, lack adequate prevention and treatment strategies.  Malaria and Tuberculosis alone kill 2 million people annually.

These diseases are called neglected because pharmaceutical companies and governments historically direct little research funding toward them by Western nations, partly because these regions are largely unaffected, which additionally makes these treatments less commercially profitable.  Addressing NTDs often also requires significant investment in local infrastructure such as access to clean water, healthy food, sanitation, mosquito netting, work safety conditions, health education and health care access. 

The World Health Organization (WHO) currently prioritizes 18 NTDs, affecting over 1 billion of the world’s poorest people.  A landmark study found that of more than 1,500 drugs that come to market between 1975 and 2004, only 10 were targeted at NTDs.  Approximately 1.4 billion people are currently affected by NTDs. 

 

The World Health Organization (WHO) prioritizes 18 neglected tropical diseases (NTDs) that affect over a billion of the world’s poorest people and pose a significant economic burden to developing economies.  NTDs don’t just affect low- and middle-income countries, although their victims are often socioeconomically disadvantaged. Cysticercosis, echinococcus, toxocariasis, Dengue virus, West Nile virus, and Chagas disease all have appeared in the United States, disproportionately afflicting the poor. Peter Hotez of the Sabin Vaccine Institute and Baylor College of Medicine has estimated that half of the 20 million people living in poverty in the US are infected with at least one NTD. ~Rachel Cotton, Harvard Immunology Program

Examples of Neglected Tropical Diseases

Chagas disease:  caused by a protozoa carried by an insect vector (triatomine bugs, also known “kissing bugs”).

Dengue fever: caused by virus transmitted through mosquito bites.

Leprosy:  caused by bacteria in airborne respiratory droplets

Helminth infections:  caused by tiny parasitic worms (e.g., Guinea-worms) that enter the body through contaminated water (consumed or waded in), through the skin or through contaminated food.

What is Epidemiology?

Epidemiology is the science of tracking the pattern and the occurrence of disease.  It is essential for planning effective prevention strategies, efficient use of health care resources, and appropriate training and deployment of health care professionals.

Prevention strategies typically include:  health education, food security, travel advisories, vaccinations, equipping health facilities with appropriate equipment and medications, and public health campaigns (e.g., hygiene strategies during cold and flu season).

Communicable Used interchangeably with infectious disease.
Notifiable Disease A disease tracked by health authorities because regular and timely information is necessary for planning prevention and control in order to maintain public safety.
Incidence The number of new cases of a disease within a population over a given time period.
Prevalence The number of new plus existing current cases of a disease within a population.  Prevalence is always higher than incidence.

Endemic, Epidemic, and Pandemic

The etymology (study of word origins) of these three terms can be helpful in remembering the difference between them.  All three share the Greek word demos meaning ‘people’.

Endemic ‘Endo-‘ (within) + ‘demos’ (people):  A disease maintained in a population at expected baseline levels without an outside source.  Example:  cold and flu viruses in Canada, which circulate year-round and peak each winter.
Epidemic ‘Epi-‘ (above) + ‘demos’ (people):  An outbreak in which a disease occurs at a higher rate than expected within a set population.  Example:  a year with unexpectedly high flu rates in Canada
Pandemic ‘Pan-‘ (all/global) + ‘demos’ (people):  An infectious disease that has spread across borders or worldwide.  Examples include the Spanish flu (1918), H1N1 flu (early 2000s), SARS-CoV1 (2003), and SARS-CoV2 (2019) also known as COVID19.
Proactive control measures can reduce peak number of cases during epidemics
Proactive control measures can reduce peak number of cases during epidemics

Notifiable Diseases in Canada and the Years Notifiable:

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