Diabetes mellitus type 2 overview: Difference between revisions

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==Overview==
==Overview==
Diabetes mellitus type 2([[T2DM]]) (formerly called non [[insulin]]-dependent [[diabetes]] (NIDDM), [[obesity]] related [[diabetes]], or adult-onset [[diabetes]]) is a [[metabolism|metabolic]] disorder that is primarily characterized by [[insulin resistance]], relative [[insulin]] [[deficiency]], and [[hyperglycemia]]. The defective responsiveness of body tissues to [[insulin]] almost certainly involves the [[insulin receptor]] in [[Cell membranes|cell membrane]]<nowiki/>s. In the early stage the predominant abnormality is reduced [[insulin sensitivity]], characterized by elevated levels of [[insulin]] in the [[blood]]. At this stage [[hyperglycemia]] can be managed by engaging in [[exercise]], modifying one's [[diet]] and [[Anti-diabetic drug|medication]]s that improve [[insulin sensitivity]] or reduce [[glucose]] production by the [[liver]]. As the [[disease]] progresses the impairment of [[insulin]] secretion worsens, and [[therapeutic]] replacement of [[insulin]] often becomes necessary. It is rapidly increasing in the developed world, and there is some evidence that this pattern will be followed in much of the rest of the world in coming years. The [[Centers for Disease Control and Prevention|CDC]] has characterized the increase as an [[epidemic]].<ref>{{Citation
[[Diabetes mellitus type 2]] ([[T2DM]]) (formerly called non [[insulin]]-dependent [[diabetes]] ([[Diabetes mellitus type 2|NIDDM]]), [[obesity]] related [[diabetes]], or adult-onset [[diabetes]]) is a [[metabolism|metabolic]] disorder that is primarily characterized by [[insulin resistance]], relative [[insulin]] [[deficiency]], and [[hyperglycemia]]. The defective responsiveness of body tissues to [[insulin]] almost certainly involves the [[insulin receptor]] in [[Cell membranes|cell membrane]]<nowiki/>s. In the early stage the predominant abnormality is reduced [[insulin sensitivity]], characterized by elevated levels of [[insulin]] in the [[blood]]. At this stage [[hyperglycemia]] can be managed by engaging in [[exercise]], modifying one's [[diet]] and [[Anti-diabetic drug|medication]]s that improve [[insulin sensitivity]] or reduce [[glucose]] production by the [[liver]]. As the [[disease]] progresses the impairment of [[insulin]] secretion worsens, and [[therapeutic]] replacement of [[insulin]] often becomes necessary. It is rapidly increasing in the developed world, and there is some evidence that this pattern will be followed in much of the rest of the world in coming years. The [[Centers for Disease Control and Prevention|CDC]] has characterized the increase as an [[epidemic]].
  | last =Gerberding
 
  | first =Julie Louise
 
  | title =Diabetes, Disabling Disease to Double by 2050
 
  | date =2007-05-24
  | year =2007
  | publisher =CDC
  | url =http://www.cdc.gov/nccdphp/publications/aag/ddt.htm }}</ref>




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==Classification==
==Classification==
[[Diabetes]] is classified in to 3 main categories.
[[Diabetes mellitus type 2|Type 2 diabetes]] doesn't have any specific [[classification]]. Although [[diabetes mellitus]] is classified in to 3 main categories:
*[[Diabetes mellitus type 1]](T1DM)
*[[Diabetes mellitus type 1]](T1DM)
*[[Diabetes mellitus type 2]]([[T2DM]])
*[[Diabetes mellitus type 2]]([[T2DM]])
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==Pathophysiology==
==Pathophysiology==
The underlying [[pathology]] is the development of [[insulin resistance]]. Contrary to [[type 1 diabetes|T1DM]], patients with [[T2DM]] sufficiently produce [[insulin]]; however, [[cellular]] response to the circulating [[insulin]] is diminished. The mechanism by which the [[insulin resistance]] develops is postulated to be influenced by both [[genetic]] and [[Environment (biophysical)|environment]]<nowiki/>al factors. Environmental influences on the [[pathogenesis]] of [[T2DM]] include high [[glycemic]] diets, [[central obesity]], older age, male gender, low-fiber diet, and high saturated [[fat]] diet.
The underlying [[pathology]] is the development of [[insulin resistance]]. Contrary to [[type 1 diabetes|T1DM]], patients with [[T2DM]] sufficiently produce [[insulin]]; however, [[cellular]] response to the circulating [[insulin]] is diminished. The mechanism by which the [[insulin resistance]] develops is postulated to be influenced by both [[genetic]] and [[Environment (biophysical)|environment]]<nowiki/>al factors. Environmental influences on the [[pathogenesis]] of [[T2DM]] include high [[glycemic]] diets, [[central obesity]], older age, male gender, low-[[Dietary fiber|fiber diet]], and high saturated [[fat]] diet.




==Causes==
==Causes==
The underlying cause of [[T2DM]] is [[insulin resistance]]. The exact cacuse of [[insulin resistance]] is not known, however several theories exist. Central obesity, aging, and high glycemic diets are most commonly implicated in the development of T2DM.
The underlying cause of [[T2DM]] is [[insulin resistance]]. The exact cause of [[insulin resistance]] is not known, however several theories exist. Central [[obesity]], [[Ageing|aging]], and high glycemic diets are most commonly implicated in the development of [[T2DM]].
==Differentiating Diabetes mellitus type 2 from other Diseases==
==Differentiating Diabetes mellitus type 2 from other Diseases==
T2DM must be differentiated from other disorders that may present with [[polyuria]], [[polydipsia]], [[weight loss]] or [[weight gain]]. Such disorders may include other forms of diabetes mellitus (e.g.T1DM, [[MODY]]) or other endocrine disorders (e.g. [[hypothyroidism]], [[Cushing's syndrome|cushings syndrome]], [[wolfram syndrome]], [[alstrom syndrome]]) or drug that can cause hyperglycemia (e.g. [[glucocorticoids]])
[[T2DM]] must be differentiated from other disorders that may present with [[polyuria]], [[polydipsia]], [[weight loss]] or [[weight gain]]. Such disorders may include other forms of [[diabetes mellitus]] (e.g.[[Diabetes mellitus type 1|T1DM]], [[MODY]]) or other [[Endocrine system|endocrine]] disorders (e.g. [[hypothyroidism]], [[cushing's syndrome]], [[wolfram syndrome]], [[alstrom syndrome]]) or drug that can cause [[hyperglycemia]] (e.g. [[glucocorticoids]])
==Epidemiology and Demographics==
==Epidemiology and Demographics==
The prevalence of T2DM(DM) is well studied in the United States and other developed countries. However, worldwide there is a large variation in the results of the population studies in developing countries and particularly in rural areas with poor access to healthcare. For this reason, diabetes is estimated to be undiagnosed in approximately 50% of adults worldwide. In the United States, African Americans, Mexican Americans, American Indians and non-Hispanic blacks are at a higher risk of developing T2DM compared to non-Hispanic whites. It is more prevalent among those older than 65 years, although there is a growing tend of childhood-onset of the disease. In 2011, 335 million people were estimated to have T2DM and that number is on a trajectory to reach over 500 million people by 2050. These figures correlate with a prevalence of approximately 5000 and 7500 per 100,000 in 2011 and 2050, respectively. T2DM is more prevalent among men than women and in countries with low to mid income levels compared to high income level countries. It is classified as a global epidemic that is growing in parallel to massive urbanization.<ref name="pmid27733282">{{cite journal| author=GBD 2015 Disease and Injury Incidence and Prevalence Collaborators| title=Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015. | journal=Lancet | year= 2016 | volume= 388 | issue= 10053 | pages= 1545-1602 | pmid=27733282 | doi=10.1016/S0140-6736(16)31678-6 | pmc=5055577 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27733282  }} </ref>
The prevalence of [[T2DM]] ([[Diabetes mellitus|DM]]) is well studied in the United States and other developed countries. However, worldwide there is a large variation in the results of the population studies in developing countries and particularly in rural areas with poor access to [[Health care|healthcare]]. For this reason, [[diabetes]] is estimated to be undiagnosed in approximately 50% of adults worldwide. In the United States, African Americans, Mexican Americans, American Indians and non-Hispanic blacks are at a higher risk of developing [[T2DM]] compared to non-Hispanic whites. It is more prevalent among those older than 65 years, although there is a growing tend of childhood-onset of the disease. In 2011, 335 million people were estimated to have [[T2DM]] and that number is on a trajectory to reach over 500 million people by 2050. These figures correlate with a prevalence of approximately 5000 and 7500 per 100,000 in 2011 and 2050, respectively. [[T2DM]] is more prevalent among men than women and in countries with low to mid income levels compared to high income level countries. It is classified as a global epidemic that is growing in parallel to massive urbanization.
<ref name="IDF">{{cite web
| url =http://www.diabetesatlas.org/
| title = IDF Diabetes Atlas 7th Edition
| location = Brussels, Belgium
| last =
| first =
| date = 2015
| website =IDF
| publisher = International Diabetes Federation
| access-date = 9 March 2017
| quote = }}</ref>


==Risk Factors==
==Risk Factors==
Common risk factors associated with development of T2DM include: positive family history, certain ethnicity, [[obesity]], [[smoking]], [[physical inactivity]], poor dietary habits, certain drugs (.eg. [[glucocorticoids]]) and certain medical conditions that may result in weight gain and inactivity.<ref name="pmid23052052">{{cite journal |vauthors=Scott RA, Langenberg C, Sharp SJ, Franks PW, Rolandsson O, Drogan D, van der Schouw YT, Ekelund U, Kerrison ND, Ardanaz E, Arriola L, Balkau B, Barricarte A, Barroso I, Bendinelli B, Beulens JW, Boeing H, de Lauzon-Guillain B, Deloukas P, Fagherazzi G, Gonzalez C, Griffin SJ, Groop LC, Halkjaer J, Huerta JM, Kaaks R, Khaw KT, Krogh V, Nilsson PM, Norat T, Overvad K, Panico S, Rodriguez-Suarez L, Romaguera D, Romieu I, Sacerdote C, Sánchez MJ, Spijkerman AM, Teucher B, Tjonneland A, Tumino R, van der A DL, Wark PA, McCarthy MI, Riboli E, Wareham NJ |title=The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: the EPIC-InterAct study |journal=Diabetologia |volume=56 |issue=1 |pages=60–9 |year=2013 |pmid=23052052 |pmc=4038917 |doi=10.1007/s00125-012-2715-x |url=}}</ref><ref name="pmid11118026">{{cite journal |vauthors=Meigs JB, Cupples LA, Wilson PW |title=Parental transmission of type 2 diabetes: the Framingham Offspring Study |journal=Diabetes |volume=49 |issue=12 |pages=2201–7 |year=2000 |pmid=11118026 |doi= |url=}}</ref><ref name="pmid12503980">{{cite journal |vauthors=Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F, Bales VS, Marks JS |title=Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001 |journal=JAMA |volume=289 |issue=1 |pages=76–9 |year=2003 |pmid=12503980 |doi= |url=}}</ref><ref name="pmid21128002">{{cite journal |vauthors=Nguyen NT, Nguyen XM, Lane J, Wang P |title=Relationship between obesity and diabetes in a US adult population: findings from the National Health and Nutrition Examination Survey, 1999-2006 |journal=Obes Surg |volume=21 |issue=3 |pages=351–5 |year=2011 |pmid=21128002 |pmc=3040808 |doi=10.1007/s11695-010-0335-4 |url=}}</ref><ref name="pmid1737857">{{cite journal |vauthors=Friedman JE, Dohm GL, Leggett-Frazier N, Elton CW, Tapscott EB, Pories WP, Caro JF |title=Restoration of insulin responsiveness in skeletal muscle of morbidly obese patients after weight loss. Effect on muscle glucose transport and glucose transporter GLUT4 |journal=J. Clin. Invest. |volume=89 |issue=2 |pages=701–5 |year=1992 |pmid=1737857 |pmc=442905 |doi=10.1172/JCI115638 |url=}}</ref><ref name="pmid7988316">{{cite journal |vauthors=Chan JM, Rimm EB, Colditz GA, Stampfer MJ, Willett WC |title=Obesity, fat distribution, and weight gain as risk factors for clinical diabetes in men |journal=Diabetes Care |volume=17 |issue=9 |pages=961–9 |year=1994 |pmid=7988316 |doi= |url=}}</ref><ref name="pmid11063954">{{cite journal |vauthors=Manson JE, Ajani UA, Liu S, Nathan DM, Hennekens CH |title=A prospective study of cigarette smoking and the incidence of diabetes mellitus among US male physicians |journal=Am. J. Med. |volume=109 |issue=7 |pages=538–42 |year=2000 |pmid=11063954 |doi= |url=}}</ref><ref name="pmid2589303">{{cite journal |vauthors=Feskens EJ, Kromhout D |title=Cardiovascular risk factors and the 25-year incidence of diabetes mellitus in middle-aged men. The Zutphen Study |journal=Am. J. Epidemiol. |volume=130 |issue=6 |pages=1101–8 |year=1989 |pmid=2589303 |doi= |url=}}</ref><ref name="pmid7888928">{{cite journal |vauthors=Rimm EB, Chan J, Stampfer MJ, Colditz GA, Willett WC |title=Prospective study of cigarette smoking, alcohol use, and the risk of diabetes in men |journal=BMJ |volume=310 |issue=6979 |pages=555–9 |year=1995 |pmid=7888928 |pmc=2548937 |doi= |url=}}</ref><ref name="pmid16186287">{{cite journal |vauthors=Foy CG, Bell RA, Farmer DF, Goff DC, Wagenknecht LE |title=Smoking and incidence of diabetes among U.S. adults: findings from the Insulin Resistance Atherosclerosis Study |journal=Diabetes Care |volume=28 |issue=10 |pages=2501–7 |year=2005 |pmid=16186287 |doi= |url=}}</ref>
Common [[Risk factor|risk factors]] associated with development of [[T2DM]] include: positive family history, certain [[Ethnicity and health|ethnicity]], [[obesity]], [[smoking]], [[physical inactivity]], poor dietary habits, certain drugs (.eg. [[glucocorticoids]]) and certain medical conditions that may result in [[weight gain]] and inactivity.
==Screening==
==Screening==
Diabetes screening is recommended for many people at various stages of life, and for those with any of several risk factors. Screening tests are the same tests used for diagnosis. Early diagnosis and treatment can control the complications and result in better clinical outcomes.
[[Diabetes]] [[Screening (medicine)|screening]] is recommended for many people at various stages of life, and for those with any of several [[Risk factor|risk factors]]. [[Screening (medicine)|Screening]] tests are the same tests used for [[diagnosis]]. Early diagnosis and treatment can control the [[Complication (medicine)|complications]] and result in better clinical outcomes.
{| style="border: 0px; font-size: 90%; margin: 3px;" align=center
{| style="border: 0px; font-size: 90%; margin: 3px;" align=center
!align="center" style="background:#DCDCDC;"|'''Criteria for testing for diabetes or prediabetes in asymptomatic adults'''
!align="center" style="background:#DCDCDC;"|'''Criteria for testing for diabetes or prediabetes in asymptomatic adults'''
|-
|-
|align="left" style="background:#F5F5F5;"|Testing should be considered in overweight or obese ([[BMI]] ≥25 kg/m2 or ≥23 kg/m2 in Asian Americans) adults who have one or more of the following risk factors:
|align="left" style="background:#F5F5F5;"|Testing should be considered in [[overweight]] or [[Obesity|obese]] ([[BMI]] ≥25 kg/m2 or ≥23 kg/m2 in Asian Americans) adults who have one or more of the following [[Risk factor|risk factors]]:
* [[A1C]]  ≥5.7% (39 mmol/mol), IGT (Impaired Glucose Tolerance), or IFG (Impaired Fasting Glucose) on previous testing
 
* First-degree relative with diabetes
*[[A1C]]  ≥5.7% (39 mmol/mol), IGT (Impaired Glucose Tolerance), or IFG (Impaired Fasting Glucose) on previous testing
* High-risk race/ethnicity (e.g., African American, Latino, Native American, Asian American,  Pacific Islander)
* First-degree relative with [[diabetes]]
* Women who were diagnosed with [[GDM]] (Gestational DM)
* High-risk race/[[Ethnicity and health|ethnicity]] (e.g., African American, Latino, Native American, Asian American,  Pacific Islander)
* Women who were diagnosed with [[GDM]] ([[Gestational diabetes|Gestational DM]])
* History of [[Cardiovascular disease|CVD]]
* History of [[Cardiovascular disease|CVD]]
* [[Hypertension]] ( ≥140/90 mmHg or on therapy for [[hypertension]])
*[[Hypertension]] ( ≥140/90 mmHg or on therapy for [[hypertension]])
* [[HDL cholesterol]] level <35 mg/dL (0.90 mmol/L) and/or a [[triglyceride]] level >250 mg/dL  (2.82 mmol/L)
*[[HDL cholesterol]] level <35 mg/dL (0.90 mmol/L) and/or a [[triglyceride]] level >250 mg/dL  (2.82 mmol/L)
* Women with [[polycystic ovary syndrome]]
* Women with [[polycystic ovary syndrome]]
* Physical inactivity
* Physical inactivity
* Other clinical conditions associated with [[insulin resistance]] (e.g., severe obesity, [[Acanthosis nigricans|acanthosis]] [[Acanthosis nigricans|nigricans]]).
* Other clinical conditions associated with [[insulin resistance]] (e.g., severe [[obesity]], [[Acanthosis nigricans|acanthosis]] [[Acanthosis nigricans|nigricans]]).
|-
|-
|align="left" style="background:#F5F5F5;"|For all patients, testing should begin at age 45 years.
|align="left" style="background:#F5F5F5;"|For all patients, testing should begin at age 45 years.
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|align="left" style="background:#F5F5F5;"|If results are normal, testing should be repeated at a minimum of 3-year intervals, with consideration of more frequent testing depending on initial results (e.g., those with
|align="left" style="background:#F5F5F5;"|If results are normal, testing should be repeated at a minimum of 3-year intervals, with consideration of more frequent testing depending on initial results (e.g., those with


prediabetes should be tested yearly) and risk status.
[[prediabetes]] should be tested yearly) and risk status.
|}
|}
==Natural History, Complications and Prognosis==
==Natural History, Complications and Prognosis==
If T2DM left untreated, it may result in [[hyperosmolar hyperglycemic state]] (HHS) and in rare circumstances [[diabetic ketoacidosis]] (DKA). These are classified as acute complications of diabetes. Chronic complications of diabetes mellitus include [[Microvascular disease|microvascular]] and [[Macrovascular disease|macrovascular]] complications. Early diagnosis and prompt treatment of these complications may result in improved prognosis and less long term [[morbidity]] and [[Mortality|mortalities]].<ref name="pmid27979887">{{cite journal |vauthors= |title=Standards of Medical Care in Diabetes-2017: Summary of Revisions |journal=Diabetes Care |volume=40 |issue=Suppl 1 |pages=S4–S5 |year=2017 |pmid=27979887 |doi=10.2337/dc17-S003 |url=}}</ref> <ref name="pmid7497874">{{cite journal |vauthors=Mogensen CE, Vestbo E, Poulsen PL, Christiansen C, Damsgaard EM, Eiskjaer H, Frøland A, Hansen KW, Nielsen S, Pedersen MM |title=Microalbuminuria and potential confounders. A review and some observations on variability of urinary albumin excretion |journal=Diabetes Care |volume=18 |issue=4 |pages=572–81 |year=1995 |pmid=7497874 |doi= |url=}}</ref><ref name="pmid24145991">{{cite journal |vauthors=Qaseem A, Hopkins RH, Sweet DE, Starkey M, Shekelle P |title=Screening, monitoring, and treatment of stage 1 to 3 chronic kidney disease: A clinical practice guideline from the American College of Physicians |journal=Ann. Intern. Med. |volume=159 |issue=12 |pages=835–47 |year=2013 |pmid=24145991 |doi=10.7326/0003-4819-159-12-201312170-00726 |url=}}</ref><ref name="pmid21115758">{{cite journal |vauthors=Colberg SR, Sigal RJ, Fernhall B, Regensteiner JG, Blissmer BJ, Rubin RR, Chasan-Taber L, Albright AL, Braun B |title=Exercise and type 2 diabetes: the American College of Sports Medicine and the American Diabetes Association: joint position statement |journal=Diabetes Care |volume=33 |issue=12 |pages=e147–67 |year=2010 |pmid=21115758 |pmc=2992225 |doi=10.2337/dc10-9990 |url=}}</ref><ref name="pmid16386666">{{cite journal |vauthors=Scognamiglio R, Negut C, Ramondo A, Tiengo A, Avogaro A |title=Detection of coronary artery disease in asymptomatic patients with type 2 diabetes mellitus |journal=J. Am. Coll. Cardiol. |volume=47 |issue=1 |pages=65–71 |year=2006 |pmid=16386666 |doi=10.1016/j.jacc.2005.10.008 |url=}}</ref><ref name="pmid16757028">{{cite journal |vauthors=Pasquale LR, Kang JH, Manson JE, Willett WC, Rosner BA, Hankinson SE |title=Prospective study of type 2 diabetes mellitus and risk of primary open-angle glaucoma in women |journal=Ophthalmology |volume=113 |issue=7 |pages=1081–6 |year=2006 |pmid=16757028 |doi=10.1016/j.ophtha.2006.01.066 |url=}}</ref>
If [[T2DM]] left untreated, it may result in [[hyperosmolar hyperglycemic state]] ([[Hyperosmolar hyperglycemic state|HHS]]) and in rare circumstances [[diabetic ketoacidosis]] ([[Diabetic ketoacidosis|DKA]]). These are classified as acute [[Complication (medicine)|complications]] of [[diabetes]]. Chronic [[Complication (medicine)|complications]] of [[diabetes mellitus]] include [[Microvascular disease|microvascular]] and [[Macrovascular disease|macrovascular]] complications. Early diagnosis and prompt treatment of these [[Complication (medicine)|complications]] may result in improved [[prognosis]] and less long term [[morbidity]] and [[Mortality|mortalities]].
==Diagnosis==
==Diagnosis==


===History and Symptoms===
===History and Symptoms===
A detailed history must be taken from every person presenting with diabetes symptoms. Classic symptoms of diabetes include: [[weight loss]], [[polyphagia]], [[polydipsia]] and [[polyuria]]. Less common symptoms include vision changes, [[tingling]] or [[numbness]] in exterimities, [[fatigue]] and skin changes.<ref name="pmid18519930">{{cite journal |vauthors= |title=Screening for type 2 diabetes mellitus in adults: U.S. Preventive Services Task Force recommendation statement |journal=Ann. Intern. Med. |volume=148 |issue=11 |pages=846–54 |year=2008 |pmid=18519930 |doi= |url=}}</ref><ref name="pmid28070960">{{cite journal |vauthors=Marathe PH, Gao HX, Close KL |title=American Diabetes Association Standards of Medical Care in Diabetes 2017 |journal=J Diabetes |volume=9 |issue=4 |pages=320–324 |year=2017 |pmid=28070960 |doi=10.1111/1753-0407.12524 |url=}}</ref>
A detailed history must be taken from every person presenting with [[diabetes]] symptoms. Classic symptoms of [[diabetes]] include: [[weight loss]], [[polyphagia]], [[polydipsia]] and [[polyuria]]. Less common symptoms include vision changes, [[tingling]] or [[numbness]] in exterimities, [[fatigue]] and skin changes.
===Physical Examination===
===Physical Examination===
Usually patients with T2DM have normal physical examination findings unless complications develop in these patients. Common physical examination findings include, pigmented skin patches and [[acanthosis nigricans]].
Usually patients with [[T2DM]] have normal physical examination findings unless [[Complication (medicine)|complications]] develop in these patients. Common physical examination findings include, pigmented skin patches and [[acanthosis nigricans]].
===Laboratory Findings===
===Laboratory Findings===
Laboratory findings of T2DM are diagnostic for this disease. Diabetes may be diagnosed based on plasma glucose criteria, either the [[fasting plasma glucose]] (FPG) or the 2-h plasma glucose (2-h PG) value after a 75-g [[oral glucose tolerance test]] (OGTT) or [[A1C]] criteria. All of these measurements are equally appropriate in diagnosis.<ref name="pmid27979887">{{cite journal |vauthors= |title=Standards of Medical Care in Diabetes-2017: Summary of Revisions |journal=Diabetes Care |volume=40 |issue=Suppl 1 |pages=S4–S5 |year=2017 |pmid=27979887 |doi=10.2337/dc17-S003 |url=}}</ref>
Laboratory findings of [[T2DM]] are diagnostic for this disease. [[Diabetes]] may be diagnosed based on [[Blood sugar|plasma glucose]] criteria, either the [[fasting plasma glucose]] (FPG) or the 2-hours [[Blood sugar|plasma glucose]] (2-h PG) value after a 75-g [[oral glucose tolerance test]] ([[Glucose tolerance test|OGTT]]) or [[A1C]] criteria. All of these measurements are equally appropriate in diagnosis.


{| style="border: 0px; font-size: 90%; margin: 3px;" align=center
{| style="border: 0px; font-size: 90%; margin: 3px;" align=center
!align="center" style="background:#DCDCDC;"|'''Criteria for the diagnosis of diabetes'''
!align="center" style="background:#DCDCDC;"|'''Criteria for the diagnosis of diabetes'''
|-
|-
|align="left" style="background:#F5F5F5;"|[[Fasting plasma glucose|FPG]]  ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8 h.
|align="left" style="background:#F5F5F5;"|[[Fasting plasma glucose|FPG]]  ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8 hours.
|-
|-
|align="center" style="background:#F5F5F5;"|'''OR'''
|align="center" style="background:#F5F5F5;"|'''OR'''
|-
|-
|align="left" style="background:#F5F5F5;"|2-h [[Blood glucose|Plasma Glucose]] (PG)  ≥200 mg/dL (11.1 mmol/L) during an [[Glucose tolerance test|OGTT]]. The test should be performed as described
|align="left" style="background:#F5F5F5;"|2-hours [[Blood glucose|Plasma Glucose]] ([[Blood sugar|PG]])  ≥200 mg/dL (11.1 mmol/L) during an [[Glucose tolerance test|OGTT]]. The test should be performed as described
by the [[WHO]], using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water.
by the [[WHO]], using a [[glucose]] load containing the equivalent of 75 g [[anhydrous]] glucose dissolved in water.
|-
|-
|align="center" style="background:#F5F5F5;"|'''OR'''
|align="center" style="background:#F5F5F5;"|'''OR'''
Line 100: Line 86:
|}
|}
==Treatment==
==Treatment==
Life style modification is fundamental for diabetes management and it's a part of therapy. It include, diabetes self-management education (DSME), diabetes self-management support (DSMS), nutrition therapy, [[physical activity]], [[smoking cessation]] counseling, and psychosocial care. The overall objectives of DSME and DSMS are to support informed decision making, self-care behaviors, problem solving, and active collaboration with the health care team to improve clinical outcomes, health status, and quality of life in a cost-effective manner.<ref name="pmid9434653">{{cite journal |vauthors=Kulkarni K, Castle G, Gregory R, Holmes A, Leontos C, Powers M, Snetselaar L, Splett P, Wylie-Rosett J |title=Nutrition Practice Guidelines for Type 1 Diabetes Mellitus positively affect dietitian practices and patient outcomes. The Diabetes Care and Education Dietetic Practice Group |journal=J Am Diet Assoc |volume=98 |issue=1 |pages=62–70; quiz 71–2 |year=1998 |pmid=9434653 |doi= |url=}}</ref><ref name="pmid20536522">{{cite journal |vauthors=Scavone G, Manto A, Pitocco D, Gagliardi L, Caputo S, Mancini L, Zaccardi F, Ghirlanda G |title=Effect of carbohydrate counting and medical nutritional therapy on glycaemic control in Type 1 diabetic subjects: a pilot study |journal=Diabet. Med. |volume=27 |issue=4 |pages=477–9 |year=2010 |pmid=20536522 |doi=10.1111/j.1464-5491.2010.02963.x |url=}}</ref><ref name="pmid20647285">{{cite journal |vauthors=Coppell KJ, Kataoka M, Williams SM, Chisholm AW, Vorgers SM, Mann JI |title=Nutritional intervention in patients with type 2 diabetes who are hyperglycaemic despite optimised drug treatment--Lifestyle Over and Above Drugs in Diabetes (LOADD) study: randomised controlled trial |journal=BMJ |volume=341 |issue= |pages=c3337 |year=2010 |pmid=20647285 |pmc=2907481 |doi= |url=}}</ref><ref name="pmid15220230">{{cite journal |vauthors=Wolf AM, Conaway MR, Crowther JQ, Hazen KY, L Nadler J, Oneida B, Bovbjerg VE |title=Translating lifestyle intervention to practice in obese patients with type 2 diabetes: Improving Control with Activity and Nutrition (ICAN) study |journal=Diabetes Care |volume=27 |issue=7 |pages=1570–6 |year=2004 |pmid=15220230 |doi= |url=}}</ref>
Life style modification is fundamental for [[diabetes]] management and it's a part of therapy. It include, [[diabetes]] self-management education (DSME), diabetes self-management support (DSMS), nutrition therapy, [[physical activity]], [[smoking cessation]] counseling, and [[psychosocial]] care. The overall objectives of DSME and DSMS are to support informed decision making, self-care behaviors, problem solving, and active collaboration with the [[health care]] team to improve clinical outcomes, health status, and quality of life in a cost-effective manner.
===Medical Therapy===
===Medical Therapy===
The main goals of treatment are, eliminate [[hyperglycemic]] symptoms, control the long term complications and improve the patient's quality of life.<ref name="pmid24145991">{{cite journal |vauthors=Qaseem A, Hopkins RH, Sweet DE, Starkey M, Shekelle P |title=Screening, monitoring, and treatment of stage 1 to 3 chronic kidney disease: A clinical practice guideline from the American College of Physicians |journal=Ann. Intern. Med. |volume=159 |issue=12 |pages=835–47 |year=2013 |pmid=24145991 |doi=10.7326/0003-4819-159-12-201312170-00726 |url=}}</ref><ref name="pmid27979887">{{cite journal |vauthors= |title=Standards of Medical Care in Diabetes-2017: Summary of Revisions |journal=Diabetes Care |volume=40 |issue=Suppl 1 |pages=S4–S5 |year=2017 |pmid=27979887 |doi=10.2337/dc17-S003 |url=}}</ref><ref name="pmid12145243">{{cite journal |vauthors=Colagiuri S, Cull CA, Holman RR |title=Are lower fasting plasma glucose levels at diagnosis of type 2 diabetes associated with improved outcomes?: U.K. prospective diabetes study 61 |journal=Diabetes Care |volume=25 |issue=8 |pages=1410–7 |year=2002 |pmid=12145243 |doi= |url=}}</ref><ref name="pmid1441492">{{cite journal |vauthors=Davidson MB |title=Successful treatment of markedly symptomatic patients with type II diabetes mellitus using high doses of sulfonylurea agents |journal=West. J. Med. |volume=157 |issue=2 |pages=199–200 |year=1992 |pmid=1441492 |pmc=1011263 |doi= |url=}}</ref><ref name="pmid27088241">{{cite journal |vauthors=Maruthur NM, Tseng E, Hutfless S, Wilson LM, Suarez-Cuervo C, Berger Z, Chu Y, Iyoha E, Segal JB, Bolen S |title=Diabetes Medications as Monotherapy or Metformin-Based Combination Therapy for Type 2 Diabetes: A Systematic Review and Meta-analysis |journal=Ann. Intern. Med. |volume=164 |issue=11 |pages=740–51 |year=2016 |pmid=27088241 |doi=10.7326/M15-2650 |url=}}</ref><ref name="pmid27434443">{{cite journal |vauthors=Palmer SC, Mavridis D, Nicolucci A, Johnson DW, Tonelli M, Craig JC, Maggo J, Gray V, De Berardis G, Ruospo M, Natale P, Saglimbene V, Badve SV, Cho Y, Nadeau-Fredette AC, Burke M, Faruque L, Lloyd A, Ahmad N, Liu Y, Tiv S, Wiebe N, Strippoli GF |title=Comparison of Clinical Outcomes and Adverse Events Associated With Glucose-Lowering Drugs in Patients With Type 2 Diabetes: A Meta-analysis |journal=JAMA |volume=316 |issue=3 |pages=313–24 |year=2016 |pmid=27434443 |doi=10.1001/jama.2016.9400 |url=}}</ref>
The main goals of treatment are, eliminate [[hyperglycemic]] symptoms, control the long term [[Complication (medicine)|complications]] and improve the patient's quality of life.
T2DM is initially treated by life style modification and [[weight loss]], especially in [[obese]] patients. [[Metformin]] is the first line pharmacologic therapy prescribed once the diagnosis is confirmed unless contraindications exist. If glycemic goals are not achieved, a second agent must be added to [[metformin]]. A wide range of options are available to add as combination therapy based on the patient's condition and comorbidities.<br>
[[T2DM]] is initially treated by life style modification and [[weight loss]], especially in [[obese]] patients. [[Metformin]] is the first line pharmacologic therapy prescribed once the diagnosis is confirmed unless [[Contraindication|contraindications]] exist. If glycemic goals are not achieved, a second agent must be added to [[metformin]]. A wide range of options are available to add as combination therapy based on the patient's condition and [[Comorbidity|comorbidities]].<br>
Medical therapy: [[Metformin]] monotherapy unless there is a contraindication to it. In the following conditions, dual therapy is initiated:
Medical therapy: [[Metformin]] monotherapy unless there is a contraindication to it. In the following conditions, dual therapy is initiated:
*[[HbA1C]] greater than 9; commence dual oral blood glucose lowering agent.
*[[HbA1C]] greater than 9 commence dual oral blood glucose lowering agent.
*[[HbA1C]] greater than 10 OR blood glucose level greater than 300 mg/dl OR a markedly symptomatic patient; consider combination therapy with [[insulin]].
*[[HbA1C]] greater than 10 OR [[Blood sugar|blood glucose]] level greater than 300 mg/dl OR a markedly symptomatic patient; consider combination therapy with [[insulin]].


===Surgery===
===Surgery===
[[Pancreas transplantation|Pancreas and islet cell transplantation]] is considered in patients with chronic diabetes who have frequent metabolic complications and are intolerant to exogenous [[insulin]] or have failed [[insulin]] therapy.<ref name="pmid16567844">{{cite journal |vauthors=Robertson RP, Davis C, Larsen J, Stratta R, Sutherland DE |title=Pancreas and islet transplantation in type 1 diabetes |journal=Diabetes Care |volume=29 |issue=4 |pages=935 |year=2006 |pmid=16567844 |doi= |url=}}</ref>
[[Pancreas transplantation|Pancreas and islet cell transplantation]] is considered in patients with chronic [[diabetes]] who have frequent metabolic [[Complication (medicine)|complications]] and are intolerant to [[exogenous]] [[insulin]] or have failed [[insulin]] therapy.
===Primary Prevention===
===Primary Prevention===
Life style modification is the mainstay for diabetes mellitus prevention. [[Metformin]] is another adjunctive measure to prevent diabetes in high risk persons. Studies have shown that 7% [[weight loss]] within a duration of 6 months in obese individuals is effective for diabetes prevention.<ref name="pmid17098085">{{cite journal |vauthors=Lindström J, Ilanne-Parikka P, Peltonen M, Aunola S, Eriksson JG, Hemiö K, Hämäläinen H, Härkönen P, Keinänen-Kiukaanniemi S, Laakso M, Louheranta A, Mannelin M, Paturi M, Sundvall J, Valle TT, Uusitupa M, Tuomilehto J |title=Sustained reduction in the incidence of type 2 diabetes by lifestyle intervention: follow-up of the Finnish Diabetes Prevention Study |journal=Lancet |volume=368 |issue=9548 |pages=1673–9 |year=2006 |pmid=17098085 |doi=10.1016/S0140-6736(06)69701-8 |url=}}</ref>
Life style modification is the mainstay for [[diabetes mellitus]] [[Prevention (medical)|prevention]]. [[Metformin]] is another adjunctive measure to prevent [[diabetes]] in high risk persons. Studies have shown that 7% [[weight loss]] within a duration of 6 months in [[Obesity|obese]] individuals is effective for diabetes prevention.
===Secondary Prevention===
===Secondary Prevention===
The most important secondary prevention strategy in T2DM is to decrease the macrovascular complications. [[Lipid]] control, [[smoking cessation]] and treatment of [[hypertension]] are the most important secondary preventive measures.
The most important secondary prevention strategy in [[T2DM]] is to decrease the [[Macrovascular disease|macrovascular]] [[Complication (medicine)|complications]]. [[Lipid]] control, [[smoking cessation]] and treatment of [[hypertension]] are the most important secondary preventive measures.


==References==
==References==
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Latest revision as of 21:20, 29 July 2020

Diabetes mellitus main page

Diabetes mellitus type 2 Microchapters

Home

Patient information

Overview

Historical Perspective

Pathophysiology

Causes

Differentiating Diabetes Mellitus Type 2 from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical therapy

Life Style Modification
Pharmacotherapy
Glycemic Control

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Seyedmahdi Pahlavani, M.D. [2],Tarek Nafee, M.D. [3]

Overview

Diabetes mellitus type 2 (T2DM) (formerly called non insulin-dependent diabetes (NIDDM), obesity related diabetes, or adult-onset diabetes) is a metabolic disorder that is primarily characterized by insulin resistance, relative insulin deficiency, and hyperglycemia. The defective responsiveness of body tissues to insulin almost certainly involves the insulin receptor in cell membranes. In the early stage the predominant abnormality is reduced insulin sensitivity, characterized by elevated levels of insulin in the blood. At this stage hyperglycemia can be managed by engaging in exercise, modifying one's diet and medications that improve insulin sensitivity or reduce glucose production by the liver. As the disease progresses the impairment of insulin secretion worsens, and therapeutic replacement of insulin often becomes necessary. It is rapidly increasing in the developed world, and there is some evidence that this pattern will be followed in much of the rest of the world in coming years. The CDC has characterized the increase as an epidemic.



Historical Perspective

Diabetes mellitus is a well-recognized disease from ancient times. In 1812 diabetes mellitus became a recognized clinical entity in The New England Journal of Medicine and Surgery. In 1889, the pancreas was identified as playing a major role in the pathogenesis of the disease. The discovery of insulin in 1921 was a major turning point in the history of diabetes when Frederick Banting and Charles Best were able to reverse the diabetic state in dogs by injecting the pancreatic isolate from healthy dogs.

Classification

Type 2 diabetes doesn't have any specific classification. Although diabetes mellitus is classified in to 3 main categories:

Pathophysiology

The underlying pathology is the development of insulin resistance. Contrary to T1DM, patients with T2DM sufficiently produce insulin; however, cellular response to the circulating insulin is diminished. The mechanism by which the insulin resistance develops is postulated to be influenced by both genetic and environmental factors. Environmental influences on the pathogenesis of T2DM include high glycemic diets, central obesity, older age, male gender, low-fiber diet, and high saturated fat diet.


Causes

The underlying cause of T2DM is insulin resistance. The exact cause of insulin resistance is not known, however several theories exist. Central obesity, aging, and high glycemic diets are most commonly implicated in the development of T2DM.

Differentiating Diabetes mellitus type 2 from other Diseases

T2DM must be differentiated from other disorders that may present with polyuria, polydipsia, weight loss or weight gain. Such disorders may include other forms of diabetes mellitus (e.g.T1DM, MODY) or other endocrine disorders (e.g. hypothyroidism, cushing's syndrome, wolfram syndrome, alstrom syndrome) or drug that can cause hyperglycemia (e.g. glucocorticoids)

Epidemiology and Demographics

The prevalence of T2DM (DM) is well studied in the United States and other developed countries. However, worldwide there is a large variation in the results of the population studies in developing countries and particularly in rural areas with poor access to healthcare. For this reason, diabetes is estimated to be undiagnosed in approximately 50% of adults worldwide. In the United States, African Americans, Mexican Americans, American Indians and non-Hispanic blacks are at a higher risk of developing T2DM compared to non-Hispanic whites. It is more prevalent among those older than 65 years, although there is a growing tend of childhood-onset of the disease. In 2011, 335 million people were estimated to have T2DM and that number is on a trajectory to reach over 500 million people by 2050. These figures correlate with a prevalence of approximately 5000 and 7500 per 100,000 in 2011 and 2050, respectively. T2DM is more prevalent among men than women and in countries with low to mid income levels compared to high income level countries. It is classified as a global epidemic that is growing in parallel to massive urbanization.

Risk Factors

Common risk factors associated with development of T2DM include: positive family history, certain ethnicity, obesity, smoking, physical inactivity, poor dietary habits, certain drugs (.eg. glucocorticoids) and certain medical conditions that may result in weight gain and inactivity.

Screening

Diabetes screening is recommended for many people at various stages of life, and for those with any of several risk factors. Screening tests are the same tests used for diagnosis. Early diagnosis and treatment can control the complications and result in better clinical outcomes.

Criteria for testing for diabetes or prediabetes in asymptomatic adults
Testing should be considered in overweight or obese (BMI ≥25 kg/m2 or ≥23 kg/m2 in Asian Americans) adults who have one or more of the following risk factors:
For all patients, testing should begin at age 45 years.
If results are normal, testing should be repeated at a minimum of 3-year intervals, with consideration of more frequent testing depending on initial results (e.g., those with

prediabetes should be tested yearly) and risk status.

Natural History, Complications and Prognosis

If T2DM left untreated, it may result in hyperosmolar hyperglycemic state (HHS) and in rare circumstances diabetic ketoacidosis (DKA). These are classified as acute complications of diabetes. Chronic complications of diabetes mellitus include microvascular and macrovascular complications. Early diagnosis and prompt treatment of these complications may result in improved prognosis and less long term morbidity and mortalities.

Diagnosis

History and Symptoms

A detailed history must be taken from every person presenting with diabetes symptoms. Classic symptoms of diabetes include: weight loss, polyphagia, polydipsia and polyuria. Less common symptoms include vision changes, tingling or numbness in exterimities, fatigue and skin changes.

Physical Examination

Usually patients with T2DM have normal physical examination findings unless complications develop in these patients. Common physical examination findings include, pigmented skin patches and acanthosis nigricans.

Laboratory Findings

Laboratory findings of T2DM are diagnostic for this disease. Diabetes may be diagnosed based on plasma glucose criteria, either the fasting plasma glucose (FPG) or the 2-hours plasma glucose (2-h PG) value after a 75-g oral glucose tolerance test (OGTT) or A1C criteria. All of these measurements are equally appropriate in diagnosis.

Criteria for the diagnosis of diabetes
FPG ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8 hours.
OR
2-hours Plasma Glucose (PG) ≥200 mg/dL (11.1 mmol/L) during an OGTT. The test should be performed as described

by the WHO, using a glucose load containing the equivalent of 75 g anhydrous glucose dissolved in water.

OR
A1C ≥6.5% (48 mmol/mol).
OR
In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose ≥200 mg/dL (11.1 mmol/L).

Treatment

Life style modification is fundamental for diabetes management and it's a part of therapy. It include, diabetes self-management education (DSME), diabetes self-management support (DSMS), nutrition therapy, physical activity, smoking cessation counseling, and psychosocial care. The overall objectives of DSME and DSMS are to support informed decision making, self-care behaviors, problem solving, and active collaboration with the health care team to improve clinical outcomes, health status, and quality of life in a cost-effective manner.

Medical Therapy

The main goals of treatment are, eliminate hyperglycemic symptoms, control the long term complications and improve the patient's quality of life. T2DM is initially treated by life style modification and weight loss, especially in obese patients. Metformin is the first line pharmacologic therapy prescribed once the diagnosis is confirmed unless contraindications exist. If glycemic goals are not achieved, a second agent must be added to metformin. A wide range of options are available to add as combination therapy based on the patient's condition and comorbidities.
Medical therapy: Metformin monotherapy unless there is a contraindication to it. In the following conditions, dual therapy is initiated:

  • HbA1C greater than 9 commence dual oral blood glucose lowering agent.
  • HbA1C greater than 10 OR blood glucose level greater than 300 mg/dl OR a markedly symptomatic patient; consider combination therapy with insulin.

Surgery

Pancreas and islet cell transplantation is considered in patients with chronic diabetes who have frequent metabolic complications and are intolerant to exogenous insulin or have failed insulin therapy.

Primary Prevention

Life style modification is the mainstay for diabetes mellitus prevention. Metformin is another adjunctive measure to prevent diabetes in high risk persons. Studies have shown that 7% weight loss within a duration of 6 months in obese individuals is effective for diabetes prevention.

Secondary Prevention

The most important secondary prevention strategy in T2DM is to decrease the macrovascular complications. Lipid control, smoking cessation and treatment of hypertension are the most important secondary preventive measures.

References

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