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Welcome to GCSE Edexcel Science revision.

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Unit C B 7: Animal coordination, control and homeostasis.

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The nervous system sends rapid electrical signals along neurones.

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Hormonal communication uses chemical messengers carried in the blood and is usually slower, with longer-lasting effects.

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Endocrine glands release hormones directly into the bloodstream.

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Blood carries a hormone around the body, but only target cells with suitable receptors respond to it.

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A target organ is an organ affected by a particular hormone.

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A hormone may affect several target tissues; it does not act on every cell it passes.

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The pituitary gland lies at the base of the brain.

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It releases F S H, L H and growth hormone, and hormones such as T S H that influence other endocrine glands.

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The thyroid gland in the neck produces thyroxine.

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The adrenal glands above the kidneys produce adrenalin; adrenaline is an alternative spelling.

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The pancreas produces insulin and glucagon.

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The ovaries produce oestrogen and progesterone; the testes produce testosterone.

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A hormone directory: target cells respond through suitable receptors.

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Growth hormone supports growth of bones and other tissues.

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Puberty involves changes in sex hormones and growth-hormone activity; it is an oversimplification to say that sex hormones alone directly make the pituitary release growth hormone.

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Homeostasis maintains a stable internal environment despite changes inside or outside the body.

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Examples include blood glucose concentration, body temperature and water balance.

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Stable does not mean perfectly unchanging: conditions fluctuate around suitable levels.

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Maintaining these levels helps cells and enzymes function effectively.

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Negative feedback reverses a change from the normal level.

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If a level rises too high, the response brings it down; if it falls too low, the response brings it up.

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The response gets smaller as the level returns towards normal.

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If a regulated level rises too far, feedback can reduce it; if it falls too far, feedback can raise it.

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The response must oppose the change, rather than amplify it.

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Negative feedback is a control mechanism, while homeostasis is the maintenance of the internal environment.

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The two terms are related but are not identical definitions.

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Thyroxine helps control metabolic rate: the rate at which chemical reactions occur in the body.

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It also supports growth and development.

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When blood thyroxine concentration is low, the hypothalamus releases more T R H, thyrotropin-releasing hormone.

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T R H stimulates the pituitary gland to release T S H, thyroid-stimulating hormone.

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T S H stimulates the thyroid gland to produce and release thyroxine into the blood.

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When thyroxine returns to a suitable level, it reduces (inhibits) further T R H release and T S H production.

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The thyroid receives less stimulation, so it does not keep producing too much thyroxine.

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This is negative feedback: the increase in thyroxine reduces the signals that caused its production.

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Do not confuse the thyroid, which makes thyroxine, with the pituitary, which makes T S H.

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Thyroxine inhibits its stimulating signals: an example of negative feedback.

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Adrenalin is released from the adrenal glands during frightening or exciting situations.

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It prepares the body for a rapid fight-or-flight response.

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It increases heart rate and blood pressure, and increases blood flow to skeletal muscles.

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This helps deliver more oxygen and glucose for respiration.

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Adrenalin stimulates the liver to break glycogen down into glucose and release glucose into the blood.

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Glycogen is a stored carbohydrate; glucose is the circulating sugar.

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Adrenalin changes where blood flows: vessels supplying skeletal muscles widen (dilate), while vessels in some other regions narrow.

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More blood reaches the muscles to support rapid activity.

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The nervous system and hormones can work together.

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An adrenalin response is a temporary preparation for activity, rather than the same long-term control pathway as thyroxine.

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The menstrual cycle prepares the uterus for a possible pregnancy.

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An egg matures and is released.

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Cycles start during puberty and stop at menopause; their length and the ages at which they start and stop vary.

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Day 1 is the first day of menstruation.

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The uterus lining is shed when hormone levels fall; menstruation is not simply the loss of an egg.

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After menstruation, the lining is repaired and thickens under the influence of oestrogen.

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It does not wait until a fixed day 11 to begin repairing.

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Ovulation is the release of an egg from an ovary.

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In a simplified 28-day cycle it occurs around day 14, but actual timing varies with the cycle.

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After ovulation, progesterone helps maintain the thickened uterus lining.

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If pregnancy does not occur, progesterone and oestrogen fall and another menstruation begins.

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Sperm can travel through the cervix and uterus to an oviduct.

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Fertilisation is the fusion of sperm and egg nuclei, usually in an oviduct, also called a fallopian tube.

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The fertilised egg divides to form an embryo as it moves towards the uterus.

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Implantation is the embryo attaching to the uterus lining; it is different from fertilisation.

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Fertilisation is associated with the time around ovulation, not a fixed day 17, 21 window.

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A textbook 28-day example cannot reliably predict an individual's fertile days.

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F S H, follicle-stimulating hormone, is released by the pituitary.

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It stimulates an ovarian follicle containing an egg to mature and encourages oestrogen production.

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The developing follicle produces oestrogen.

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Oestrogen repairs and thickens the uterus lining and inhibits F S H for much of the cycle.

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A high oestrogen level just before ovulation stimulates an L H surge.

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This is a change in its feedback effect; do not assume oestrogen always inhibits every pituitary hormone.

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The pituitary releases L H (luteinising hormone).

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A sharp rise in L H triggers ovulation.

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The emptied follicle then forms a structure called the corpus luteum.

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After ovulation, the corpus luteum produces progesterone.

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This maintains the uterus lining and reduces (inhibits) F S H and L H release, helping prevent another follicle maturing and another egg being released in the same cycle.

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If pregnancy does not occur, the corpus luteum breaks down and progesterone and oestrogen decrease.

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The lining is shed and reduced inhibition allows F S H to rise for the next cycle.

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Sequence if pregnancy does not occur; actual cycle lengths and timings vary.

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When interpreting a hormone graph, look for an oestrogen rise before ovulation, a sharp L H surge around ovulation and a progesterone rise afterwards.

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These are schematic patterns, not identical curves in every person.

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Contraception reduces the chance of pregnancy.

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Different methods act in different ways, so preventing ovulation and blocking sperm should not be described as the same mechanism.

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The combined contraceptive pill contains oestrogen and a progestogen, which acts like progesterone.

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These hormones suppress pituitary F S H and L H and prevent ovulation.

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Progestogen can also thicken cervical mucus, making it harder for sperm to pass.

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Hormonal methods can include pills, patches, injections and implants; their mechanisms and suitability vary.

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A condom is a barrier that prevents semen and sperm entering the vagina when used correctly.

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Condoms also reduce transmission of many sexually transmitted infections; hormonal contraception does not provide that protection.

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A diaphragm covers the cervix and is used with spermicide to reduce sperm entry into the uterus.

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It does not stop the ovaries releasing eggs.

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Evaluate a method using effectiveness, correct use, possible side effects, how long it lasts, reversibility and protection against infections.

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No method should be described as guaranteed to prevent every pregnancy.

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A daily pill requires consistent use; a long-acting method reduces that daily requirement but can need a healthcare procedure.

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Barrier methods avoid altering the menstrual hormones but also depend on correct use.

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Assisted reproductive technology, or ART, can help some people with fertility problems.

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The approach depends on the cause of the difficulty and does not guarantee a pregnancy.

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Clomifene is a fertility medicine that can encourage ovulation in people who do not ovulate regularly.

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It promotes pituitary release of F S H and L H by reducing the effect of oestrogen feedback.

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In I V F, in vitro fertilisation, fertility hormones such as F S H stimulate development of several follicles.

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A hormone trigger, often acting like L H, helps eggs complete maturation before collection.

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Eggs are collected and fertilised with sperm in a laboratory.

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Embryos are allowed to develop before a selected embryo is transferred into the uterus.

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Progesterone can be given to help support the uterus lining after embryo transfer.

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Laboratory fertilisation and transfer do not guarantee implantation or a live birth.

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IVF involves laboratory fertilisation followed by embryo transfer.

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Benefits include the possibility of pregnancy despite some fertility problems.

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Limitations include cost, physical and emotional demands, variable success and risks such as excessive ovarian stimulation or multiple pregnancy.

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Evaluate success using comparable data and the stated outcome, such as pregnancy or live birth.

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Age and the cause of infertility can affect success, so results from different groups are not automatically comparable.

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Blood glucose concentration rises after absorption of carbohydrate from food and can fall as cells use glucose.

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The pancreas monitors and responds to these changes.

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When blood glucose is high, the pancreas releases more insulin.

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Insulin promotes glucose uptake by body cells and promotes conversion of glucose into glycogen in the liver and muscles.

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As blood glucose returns towards a suitable level, insulin secretion decreases.

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This is a negative-feedback response to an increase in glucose.

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When blood glucose is low, the pancreas releases more glucagon.

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Glucagon stimulates the liver to break glycogen down into glucose and release it into the bloodstream.

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As blood glucose rises towards a suitable level, glucagon secretion decreases.

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Insulin and glucagon therefore have opposing effects on blood glucose.

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Insulin and glucagon have opposing effects; secretion decreases as glucose returns towards normal.

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Glucose and glycogen are not interchangeable names: glucose is a small sugar that circulates in blood, while glycogen is a storage carbohydrate made from glucose units.

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Glucagon and glycogen are also different: glucagon is a hormone, while glycogen is a stored carbohydrate.

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The liver can supply glucose to the blood between meals.

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In type 1 diabetes, the body's immune system destroys insulin-producing pancreatic cells, so little or no insulin is produced.

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Blood glucose can become too high.

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Type 1 diabetes is controlled with insulin delivered by injections or a pump, together with blood-glucose monitoring and appropriate management of food and activity.

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Diet alone cannot replace the missing insulin.

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In type 2 diabetes, cells respond less effectively to insulin, and the pancreas may also produce insufficient insulin.

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This is often described as insulin resistance.

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Type 2 diabetes may be managed with dietary changes, physical activity and medicines; some people also need insulin.

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It should not be described as always controlled by diet and exercise alone.

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A higher body mass and greater abdominal fat are associated with increased type 2 diabetes risk, but genetics, age and other factors also matter.

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Type 2 diabetes can occur without obesity.

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Glucose may appear in urine if blood glucose becomes high enough.

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This can be a sign of diabetes, but a urine result alone cannot confirm a diagnosis.

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Body mass index, B M I, is calculated as mass in kilograms divided by height in metres squared: B M I  equals  mass (kg) divided by [height (m)]squared.

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For a mass of eighty one kilograms and height of one point eight zero metres, body mass index equals eighty one divided by one point eight zero squared, which equals twenty five.

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Square the height before dividing, and convert centimetres to metres first.

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Common adult categories are below 18.5: underweight; 18.5 to below 25: healthy-weight range; 25 to below 30: overweight; 30 or above: obesity.

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These adult boundaries are not used directly to assess children and teenagers, whose age and sex are considered.

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Waist:hip ratio  equals  waist circumference divided by hip circumference.

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Use the same units for both measurements; the ratio has no unit.

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For a waist of 80 centimetres and hips of 100 centimetres, the ratio is 0.80.

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A greater proportion of abdominal fat is associated with increased type 2 diabetes risk.

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A positive correlation means that higher values of one variable tend to occur with higher values of another.

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A trend between B M I and diabetes risk is not proof that every person with a high B M I will develop diabetes.

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B M I does not distinguish muscle from fat or show where fat is stored.

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Waist:hip ratio provides different information, but neither measure alone describes an individual's complete health or proves causation.

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Compare diabetes risk using proportions or percentages when group sizes differ.

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Ten cases out of 100 people and ten cases out of 1,000 people are different rates despite the same case count.

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Percentage  equals  number in a group divided by total number times 100.

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For example, 12 cases in 200 people is 6 percent; state which population the percentage describes.

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Check whether differences in age, activity or other factors could affect a reported correlation.

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A large sample and comparable groups support a more reliable comparison.

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Benedict's test can investigate reducing sugars in simulated urine: add Benedict's reagent and warm in a hot-water bath under school instructions.

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A colour change from blue towards green, yellow, orange or brick-red indicates reducing sugar.

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Benedict's reagent detects reducing sugars, not only glucose.

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Use simulated samples, appropriate eye protection and controlled heating; compare with a known positive and a negative control.

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A colour test on a simulated sample illustrates the chemistry of sugar detection.

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It does not diagnose diabetes or replace blood-glucose monitoring.

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That completes Animal coordination, control and homeostasis.

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Revisit the notes and test yourself on the revision website.
