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Review

Psychological Backgrounds of Medically Compromised Patients and Its Implication in Dentistry: A Narrative Review

1
Division of Oral Medicine and Pathology, Department of Human Biology and Pathophysiology, School of Dentistry, Health Sciences University of Hokkaido, Hokkaido 061-0293, Japan
2
Division of Disease Control and Molecular Epidemiology, Department of Oral Growth and Development, School of Dentistry, Health Sciences University of Hokkaido, Hokkaido 061-0293, Japan
3
Department of Psychosomatic Internal Medicine, Health Sciences University of Hokkaido Hospital, Hokkaido 002-8072, Japan
4
Department of Psychosomatic Dentistry, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8510, Japan
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2021, 18(16), 8792; https://doi.org/10.3390/ijerph18168792
Submission received: 5 July 2021 / Revised: 17 August 2021 / Accepted: 18 August 2021 / Published: 20 August 2021
(This article belongs to the Collection Relationships between Oral Health Management and Systemic Health)

Abstract

:
The number of medically compromised dental patients is increasing every year with the increase in the super-aged population. Many of these patients have underlying psychiatric problems and diseases, which need to be recognized by dental professionals for better treatment outcomes. The aim of this narrative review article is to summarize the psychological and psychiatric backgrounds of medically compromised patients who are frequently visited and taken care of by dentists using findings from recent systematic reviews and meta-analyses. Anxiety and symptoms of depression, post-traumatic stress disorders, panic disorders, poor cognitive functions, and poor quality of life were some of the common psychological backgrounds in medically compromised patients. Additionally, the consequences of these psychological problems and the considerations that need to be taken by the dentist while treating these patients have been discussed. Dental professionals should be aware of and recognize the different psychological backgrounds of medically compromised dental patients in order to provide appropriate dental treatment and to prevent oral conditions from worsening.

1. Introduction

The number of medically compromised patients is growing with the advance in the super-aged society in developed countries [1]. These patients need to be visited by a dentist more often with each progressing year. There are well established guidelines for how dentists see medically compromised patients for dental treatment [2]. Medically compromised patients may require regular prescriptions for their diseases or may experience an event that can interfere with their daily life. Many of these patients often have underlying psychological problems [3,4,5,6,7,8,9,10]. Dentists generally focus on dental problems, and the psychological backgrounds of these patients might often be neglected. The patient’s motivation and their self-efficacy, which can be affected by their psychology, are important for the prevention and treatment of dental diseases.
The aim of this review is to summarize the psychological backgrounds of commonly encountered medically compromised conditions in dental patients. Previous studies have shown that cardiovascular diseases such as hypertension and heart disease as well as diabetes are among the five most prevalent medically compromised conditions in dental patients [11]. Renal diseases have high global prevalence, occurring in nearly 10% of the population [12]. Additionally, connective tissue disease has a prevalence ranging from 5–30% after 65 years of age [13]. Based on these findings and our clinical experience, we selected four medically compromised conditions; diabetes, cardiovascular disease, renal disease, and connective tissue disease and reviewed the psychological status of the patients. Various psychological backgrounds in these diseases are discussed with reference to findings from recent systematic reviews and meta-analyses. The consequences of psychological status and the considerations that need to be taken by the dentist while treating these patients have also been discussed in this review.

2. Materials and Methods

An electronic search was made on PubMed using the following search terms for each of four diseases: (diabetes) AND (psychology), (cardiovascular disease) AND (psychology), (renal disease) AND (psychology), (connective tissue disease) AND (psychology). Articles in English and that had been published within the last 5 years were included (March 2015–March 2020). The studies were limited to systematic reviews and meta-analyses (Details in Supplementary Materials File S1). These articles formed the basis to show the psychological status of medically compromised patients. A few manually searched articles were also included in the review to discuss the implications of psychological background in dental treatment.

3. Results and Discussion

3.1. Diabetes

Diabetes is one of the four main non-communicable diseases (cardiovascular diseases, cancer, chronic respiratory diseases, and diabetes) and has a global prevalence of 8.5% among adults aged 18 years of age and older [14]. Some of the oral manifestations of diabetes include periodontal diseases, dental caries, candidiasis, burning sensation, altered taste, glossitis, and dry mouth [15]. The relationship between periodontal disease and diabetes is known to be bidirectional [16]. Diabetic patients have a high risk of periodontal diseases; the treatment of periodontal diseases in these patients may lead to a decrease in their blood glucose level [16].
Psychological approaches are often used in diabetic patients because they often suffer from psychological problems [17]. The psychological problems in diabetic patients might be due to diabetic distress [18], which is an emotional response to the burdens of living with diabetes and the self-care necessary to manage the condition. Diabetes-related distress has been reported in 36% of patients with type 2 diabetes [3]. Table 1 illustrates various psychological backgrounds of patients with diabetes [3,4,18,19,20,21,22,23,24,25,26,27,28,29,30,31]. The major psychological condition in diabetes includes depression and anxiety symptoms [4,26]. The pooled prevalence of depressive and anxiety symptoms in type 1 diabetic youth was shown to be 30% and 32%, respectively [32]. A large cohort study showed that the prevalence of major depression in diabetic patients was twice that in healthy individuals [33]. Moreover, diabetic patients showed poor cognitive performance [19,20,21,31] and may have a higher risk of dementia [34]. Severe hypoglycemia in type 2 diabetes was associated with increased fear of hypoglycemia, decreased emotional well-being and health status, and a diabetes-specific quality of life [35,36].
These psychological and psychiatric problems may complicate diabetic-related cardiovascular diseases, blood glucose level, and may worsen the quality of life [37]. Depression in patients with diabetes has been associated with increased risks for micro- and macrovascular complications and neuropathy [29,38]. Microvascular complications include retinopathy, neuropathy, and diabetic foot, whereas macrovascular complications include stroke, angina, cardiovascular diseases, and myocardial infarction. Furthermore, anxiety and stress may worsen the diabetic condition in these patients.
The effect of different types of psychological and psychiatric problems, including depressive conditions, may be seen during oral health and treatment. Depressive conditions in diabetes often decrease self-efficacy and the capacity for self-management [39], which might also lead to poor oral hygiene. Moreover, poor cognitive functions such as poor attention, slow psychomotor function, and poor processing speed in patients with diabetes compared to healthy individuals should be taken into consideration while planning dental treatment [19,31]. The increased risk of microvascular neuropathy in diabetic patients with depression should also be considered in dental treatment. Thus, dental professionals may need to recognize the psychological and psychiatric backgrounds of each diabetic patient in the dental setting.

3.2. Cardiovascular Diseases

Cardiovascular diseases are the number one cause of global death, constituting nearly one third of all global deaths [40]. Cardiovascular diseases include coronary heart disease, cerebrovascular disease, peripheral arterial disease, rheumatic heart disease, congenital heart disease, deep vein thrombosis, and pulmonary embolism. Acute events such as heart attack and stroke resulting from one or more cardiovascular diseases account for the majority of deaths and disabilities [40]. Dental professionals are generally cautious about underlying cardiovascular diseases during dental treatment. These patients need special care, mainly during oral surgical procedures and during medication administration. Blood pressure maintenance, hemorrhage prevention, and effects due to use of anticoagulants or anti-thrombin medications are often challenging during dental treatment in these patients [41].
Stress is a major exacerbation factor for hypertension, cardiac diseases, and arteriosclerosis [42,43]. Table 2 shows the psychological backgrounds of patients with cardiovascular diseases [5,6,42,43,44,45,46,47,48,49,50,51,52,53]. Anxiety and depression are major psychological factors in patients with cardiovascular diseases [5,48,49]. Furthermore, patients with cardiovascular diseases often have post-traumatic stress disorder (PTSD) induced by the event of a heart attack [6,50] and may experience anticipatory anxiety, which could be linked to other types of anxiety and depression. A recent meta-analysis showed a random-effects pooled prevalence of 13.1% for anxiety disorders, 28.79% for probable clinically significant anxiety, and 55.5% for elevated symptoms of anxiety among patients with heart failure [48]. The prevalence of depressive symptoms in males and females with coronary heart diseases was 23.47% and 35.75%, respectively, at the time of hospital admission [54]. The risk of developing depression in patients with coronary artery disease was 2.8 times higher than that in healthy individuals [55]. Patients with ischemic heart disease must practice self-care methods to prevent the occurrence of events, which can become a new stressor. These stresses in combination with anticipatory anxiety may be responsible for the high prevalence of anxiety and depression in patients with cardiovascular diseases.
Both anxiety and depression are associated with an increased risk of mortality in patients with coronary artery diseases [53]. Depression is an independent predictor of all-cause mortality and might be a marker of severe heart failure [44,56]. Depression is also closely related to hypertension; depressive symptoms have been known to induce hypertension [57], and about 40.1% of hypertensive patients are reported to suffer from depression [58]. Hypertensive patients with depression have poor health status and a lower quality of life and demonstrate decreased treatment compliance [45]. Several review articles have indicated that cardiovascular diseases often induce psychological problems. Patients with arrhythmia frequently experience anxiety, whereas patients with paroxysmal atrial fibrillation often present with avoidant behavior due to fear of paroxysm [59]. Furthermore, patients with implantable cardiac defibrillators are fearful of electric shock [60].
Patients with cardiovascular diseases often experience several levels of anxiety and depression. Those suffering from anxiety and depression often have less distress tolerance, which may cause dental phobia [61]. Furthermore, stressful conditions such as dental treatments may worsen their psychological problems. Depression in cardiovascular disease is associated with decreased treatment compliance and non-adherence to medication, which may affect the prognosis of dental treatment [45,46]. Poor cognitive outcomes such as non-verbal reasoning, processing speed and attention, psychomotor abilities, and numeracy in patients with cardiovascular diseases may require consideration in dental treatment [47,62].

3.3. Renal Diseases

Renal diseases are among significant contributors to morbidity and mortality from non-communicable diseases globally [63]. Nation surveys in Australia, Norway, and the USA showed that at least 10% of the adult population have markers for kidney disease. A global prevalence of 9.1% has been shown for cases of all-stage chronic kidney diseases (CKD) [12]. Dental professionals commonly encounter renal patients during dental treatment and should be cautious of their tendency for hemorrhage and the increased susceptibility to infection in dialysis patients [64,65]. Additionally, certain drugs involved in renal metabolism have to be carefully prescribed for such patients [65].
CKD is characterized by a gradual loss of kidney function requiring frequent dialysis, which impairs the activities of daily living. Dialysis patients are at a significant increased risk for sarcopenia and frailty [66] and are under constant psychological stress. Many of these patients experience psychological and psychiatric problems, and the study of the psychological factors in these patients has been termed as “psychonephrology” [67]. The psychological backgrounds of patients with renal diseases are shown in Table 3 [7,8,68,69,70,71,72,73,74,75]. Dialysis patients without any psychiatric history often develop sleep disturbances, depression, anxiety, delirium, dementia, and restless leg syndrome [67]. Depression was reported as one of the most prevalent mental diseases in hemodialysis patients, and the depressive symptoms were found to be closely associated with malnutrition [7]. A previous study showed a pooled prevalence of 62% for depressive symptoms in patients undergoing hemodialysis [68]. The depressive symptoms in CKD patients might be due to these negative emotions and distress [69] as well as the malnutrition in those undergoing hemodialysis. Physical disorders such as uremia, hypercalcemia, and cerebrovascular damage, along with psychological stress, can also cause depressive symptom [76]. Furthermore, medications such as steroids, interferon, antihypertensive drugs, and anti-parkinsonism drugs can induce depression in CKD patients [77].
The depression symptoms in dialysis patients may demonstrate decreased adherence to treatment, which affects oral health care. Studies have shown that social support from family and health care professionals is associated with treatment adherence in CKD patients [75]. The treatment adherence of patient is an important factor in successful dental treatment. Dialysis patients are at increased risk of developing dementia [67], which may present with an increased risk for physical frailty, including oral frailty [78]. CKD has a significant impact on cognition, which might diminish the ability of the patient to make health care decisions [72]; this factor should be considered during dental treatment. Thus, dental professionals must be aware of the psychological and psychiatric background of patients with renal diseases, particularly those undergoing dialysis, in a dental setting.

3.4. Connective Tissue Diseases

Connective tissue diseases refer to a group of heterogenous and immunologically mediated disorders such as rheumatoid arthritis, systemic lupus erythematosus, systemic sclerosis, and Sjogren’s syndrome. The prevalence ranges from 5–30% after the age of 65 years [13]. Oral manifestations may appear during the early phases of these diseases, and dental professionals may need to identify, manage, and refer accordingly.
The oral symptoms in connective tissue diseases mainly manifest as xerostomia and aphthous stomatitis. Those patients with connective tissue diseases and who are taking steroids have an increased susceptibility to infections and are at a high risk for the progression of periodontal diseases and opportunistic infections such as candidiasis [79,80]. Moreover, patients with hyposalivation are prone to oral infections [81]. Chronic inflammation in patients with connective tissue diseases induces fatigue and stress, and these diseases may be involved in the development of psychiatric diseases caused by neuritis [82].
The psychological backgrounds of patients with connective tissue diseases are shown in Table 4 [9,83,84,85,86,87,88,89,90,91]. Fatigue associated with psychosocial factors, such as depression, pain, and sleep disorders, were the most prevalent symptom in patients with connective tissue diseases [84]. Each type of connective tissue disease is associated with a different type of psychological problem. Rheumatoid arthritis patients experience fatigue [84,86] and poor cognitive function [90] and need to be treated for issues such as negative emotions, anxiety, and depression. Therapeutic interventions for immunological disorders improve both depression and the pathological condition in patients with rheumatoid arthritis, indicating that immunological disorders may be involved in causing depression in these patients [92]. Patients with systemic lupus erythematosus (SLE) frequently present with various types of psychiatric problems, such as impaired consciousness, anxiety disorders, cognitive disorders, mood disorders, and schizophrenia-like psychosis, which are collectively termed as neuropsychiatric SLE (NPSLE) [93,94]. Sjögren’s syndrome, a collagen-related disease, affects the senses of smell and taste, sexual function, and quality of life [88]; Approximately 33.8% and 36.9% of patients with this syndrome were reported to experience anxiety and depression, respectively [95]. The odds ratio of depression in patients with Sjögren’s syndrome, when compared to that of healthy individuals, was 5.32 [95]. Patients with connective tissue diseases who take steroid medications often have mood disorders and hallucinations, which is termed as “steroid psychosis” [96]. A high dose of steroids frequently induces this condition in patients, making it difficult for the clinician to ascertain the cause of the symptoms [97].
Patients with connective tissue diseases may have complex psychiatric problems because both immunological disorders and psychological stress can induce psychiatric diseases. Patients with connective tissue diseases often experience fatigue, which is associated with psychosocial factors such as pain, depression, sleep disorders, and low mood [84,85,86]. These factors should be considered during dental treatment. Previous studies have shown a significant association between the oropharyngeal manifestations of systemic sclerosis (assessed as maximal mouth opening and mouth handicap in systemic sclerosis scale) and impaired quality of life [89]. These factors are particularly of a dentist’s concern and should be considered during the dental treatment of these patients.

4. Psychology and Its Implication in Dentistry

The effect of various psychological backgrounds of patients with diabetes, cardiovascular diseases, renal diseases, and connective tissue diseases in dental treatment have been discussed in this article. The most common psychological states in those patients were anxiety, depression, post-traumatic stress disorders, panic disorders, poor cognitive functions, and poor quality of life. In general, psychological stress, anxiety, and depression have been linked to many oral mucosal diseases, such as burning mouth syndrome, lichen planus, and the recurrence aphthous stomatitis [98,99,100]. Psychological stresses have also been associated with periodontal diseases [101] and dental caries [102]. Negative human behavior such as low self-efficacy in adverse psychological conditions might worsen the oral environment [103]. A systematic review and meta-analysis studying the effect of psychological state on oral health showed that all of the psychiatric diagnoses were associated with increased dental caries and tooth loss on the mean number of decayed, missing, and filled teeth (DMFT) or surfaces (DMFS) scores (OR = 1.22; 95%CI = 1.14–1.30) [104]. The psychological states of medically compromised patients could therefore affect the oral health. The periodic monitoring of oral health and needful intervention at earlier stages of oral disease might be important.
The limitation of our study is that it is a narrative review and strict study selection criteria were not followed. The results of systematic reviews and meta-analyses were cited to discuss the possible psychological backgrounds of medically compromised patients. The studies highlighting the psychological status of dental patients with medically compromised conditions are very limited, and this topic needs to be further studied.

5. Conclusions

This review focused on the psychological and psychiatric backgrounds of medically compromised dental patients, i.e., those with diabetes, cardiovascular disease, renal disease, and connective tissue diseases. The psychological backgrounds of medically compromised patient are diverse. Dental professionals should be aware of and recognize these backgrounds in addition to the systemic conditions in order to provide the appropriate dental treatment and to prevent the oral conditions from worsening.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ijerph18168792/s1, File S1: Search strategy.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Lamster, I.B. Geriatric periodontology: How the need to care for the aging population can influence the future of the dental profession. Periodontol. 2000 2016, 72, 7–12. [Google Scholar] [CrossRef]
  2. The ADA Practical Guide to Patients with Medical Conditions; Patton, L.L.; Glick, M. (Eds.) John Wiley & Sons, Inc.: Hoboken, NJ, USA, 2015; ISBN 9781119121039. [Google Scholar]
  3. Perrin, N.E.; Davies, M.J.; Robertson, N.; Snoek, F.J.; Khunti, K. The prevalence of diabetes-specific emotional distress in people with Type 2 diabetes: A systematic review and meta-analysis. Diabet. Med. 2017, 34, 1508–1520. [Google Scholar] [CrossRef] [PubMed]
  4. Tong, A.; Wang, X.; Li, F.; Xu, F.; Li, Q.; Zhang, F. Risk of depressive symptoms associated with impaired glucose metabolism, newly diagnosed diabetes, and previously diagnosed diabetes: A meta-analysis of prospective cohort studies. Acta Diabetol. 2016, 53, 589–598. [Google Scholar] [CrossRef] [PubMed]
  5. Doyle, F.; McGee, H.; Conroy, R.; Conradi, H.J.; Meijer, A.; Steeds, R.; Sato, H.; Stewart, D.E.; Parakh, K.; Carney, R.; et al. Systematic Review and Individual Patient Data Meta-Analysis of Sex Differences in Depression and Prognosis in Persons with Myocardial Infarction. Psychosom. Med. 2015, 77, 419–428. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Akosile, W.; Colquhoun, D.; Young, R.; Lawford, B.; Voisey, J. The association between post-traumatic stress disorder and coronary artery disease: A meta-analysis. Australas. Psychiatry 2018, 26, 524–530. [Google Scholar] [CrossRef] [Green Version]
  7. Gebrie, M.H.; Ford, J. Depressive symptoms and dietary non-adherence among end stage renal disease patients undergoing hemodialysis therapy: Systematic review. BMC Nephrol. 2019, 20, 429. [Google Scholar] [CrossRef] [Green Version]
  8. Supelana, C.; Annunziato, R.A.; Kaplan, D.; Helcer, J.; Stuber, M.L.; Shemesh, E. PTSD in solid organ transplant recipients: Current understanding and future implications. Pediatr. Transplant. 2016, 20, 23–33. [Google Scholar] [CrossRef] [Green Version]
  9. Quilter, M.; Hiraki, L.; Korczak, D. Depressive and anxiety symptom prevalence in childhood-onset systemic lupus erythematosus: A systematic review. Lupus 2019, 28, 878–887. [Google Scholar] [CrossRef]
  10. Matcham, F.; Rayner, L.; Steer, S.; Hotopf, M. The prevalence of depression in rheumatoid arthritis: A systematic review and meta-analysis. Rheumatology 2013, 52, 2136–2148. [Google Scholar] [CrossRef] [Green Version]
  11. Dhanuthai, K.; Sappayatosok, K.; Bijaphala, P.; Kulvitit, S.; Sereerat, T. Prevalence of medically compromised conditions in dental patients. Med. Oral Patol. Oral Cir. Bucal. 2009, 14, E287–E291. [Google Scholar]
  12. GBD Chronic Kidney Disease Collaboration. Global, regional, and national burden of chronic kidney disease, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet 2020, 395, 709–733. [Google Scholar] [CrossRef] [Green Version]
  13. Spagnolo, P.; Cordier, J.-F.; Cottin, V. Connective tissue diseases, multimorbidity and the ageing lung. Eur. Respir. J. 2016, 47, 1535–1558. [Google Scholar] [CrossRef] [Green Version]
  14. World Health Organization. Diabetes. WHO Fact Sheets. 2020. Available online: https://www.who.int/news-room/fact-sheets/detail/diabetes (accessed on 22 May 2021).
  15. Albert, D.A.; Ward, A.; Allweiss, P.; Graves, D.T.; Knowler, W.C.; Kunzel, C.; Leibel, R.L.; Novak, K.F.; Oates, T.W.; Papapanou, P.N.; et al. Diabetes and oral disease: Implications for health professionals. Ann. N. Y. Acad. Sci. 2012, 1255, 1–15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  16. Preshaw, P.M.; Alba, A.L.; Herrera, D.; Jepsen, S.; Konstantinidis, A.; Makrilakis, K.; Taylor, R. Periodontitis and diabetes: A two-way relationship. Diabetologia 2012, 55, 21–31. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Price, H.C.; Ismail, K.; Allan, B.; Castro, E.; Dashora, U.; Dhatariya, K.; Flanagan, D.; George, S.; Gregory, R.; James, J.; et al. Royal College of Psychiatrists Liaison Faculty & Joint British Diabetes Societies (JBDS): Guidelines for the management of diabetes in adults and children with psychiatric disorders in inpatient settings. Diabet. Med. 2018, 35, 997–1004. [Google Scholar] [CrossRef] [PubMed]
  18. Hagger, V.; Hendrieckx, C.; Sturt, J.; Skinner, T.C.; Speight, J. Diabetes Distress Among Adolescents with Type 1 Diabetes: A Systematic Review. Curr. Diab. Rep. 2016, 16, 9. [Google Scholar] [CrossRef] [PubMed]
  19. Chen, Y.; Liu, Z.; Yu, Y.; Yao, E.; Liu, X.; Liu, L. Effect of recurrent severe hypoglycemia on cognitive performance in adult patients with diabetes: A meta-analysis. Curr. Med. Sci. 2017, 37, 642–648. [Google Scholar] [CrossRef] [PubMed]
  20. Niermeyer, M.A. Cognitive and gait decrements among non-demented older adults with Type 2 diabetes or hypertension: A systematic review. Clin. Neuropsychol. 2018, 32, 1256–1281. [Google Scholar] [CrossRef] [PubMed]
  21. Li, W.; Huang, E.; Gao, S. Type 1 Diabetes Mellitus and Cognitive Impairments: A Systematic Review. J. Alzheimer’s Dis. 2017, 57, 29–36. [Google Scholar] [CrossRef] [Green Version]
  22. Smith, K.J.; Deschênes, S.S.; Schmitz, N. Investigating the longitudinal association between diabetes and anxiety: A systematic review and meta-analysis. Diabet. Med. 2018, 35, 677–693. [Google Scholar] [CrossRef] [Green Version]
  23. Sui, H.; Sun, N.; Zhan, L.; Lu, X.; Chen, T.; Mao, X. Association between Work-Related Stress and Risk for Type 2 Diabetes: A Systematic Review and Meta-Analysis of Prospective Cohort Studies. PLoS ONE 2016, 11, e0159978. [Google Scholar] [CrossRef]
  24. Xu, T.; Magnusson Hanson, L.L.; Lange, T.; Starkopf, L.; Westerlund, H.; Madsen, I.E.H.; Rugulies, R.; Pentti, J.; Stenholm, S.; Vahtera, J.; et al. Workplace bullying and violence as risk factors for type 2 diabetes: A multicohort study and meta-analysis. Diabetologia 2018, 61, 75–83. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Jing, X.; Chen, J.; Dong, Y.; Han, D.; Zhao, H.; Wang, X.; Gao, F.; Li, C.; Cui, Z.; Liu, Y.; et al. Related factors of quality of life of type 2 diabetes patients: A systematic review and meta-analysis. Health Qual. Life Outcomes 2018, 16, 189. [Google Scholar] [CrossRef] [PubMed]
  26. Amiri, S.; Behnezhad, S. Diabetes and anxiety symptoms: A systematic review and meta-analysis. Int. J. Psychiatry Med. 2019. [Google Scholar] [CrossRef] [PubMed]
  27. Kioskli, K.; Scott, W.; Winkley, K.; Kylakos, S.; McCracken, L.M. Psychosocial Factors in Painful Diabetic Neuropathy: A Systematic Review of Treatment Trials and Survey Studies. Pain Med. 2019, 20, 1756–1773. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Danna, S.M.; Graham, E.; Burns, R.J.; Deschênes, S.S.; Schmitz, N. Association between Depressive Symptoms and Cognitive Function in Persons with Diabetes Mellitus: A Systematic Review. PLoS ONE 2016, 11, e0160809. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Nouwen, A.; Adriaanse, M.C.; Dam, K.; Iversen, M.M.; Viechtbauer, W.; Peyrot, M.; Caramlau, I.; Kokoszka, A.; Kanc, K.; Groot, M.; et al. Longitudinal associations between depression and diabetes complications: A systematic review and meta-analysis. Diabet. Med. 2019, 36, 1562–1572. [Google Scholar] [CrossRef] [PubMed]
  30. Wang, B.; An, X.; Shi, X.; Zhang, J. Management of endocrine disease: Suicide risk in patients with diabetes: A systematic review and meta-analysis. Eur. J. Endocrinol. 2017, 177, R169–R181. [Google Scholar] [CrossRef]
  31. He, J.; Ryder, A.G.; Li, S.; Liu, W.; Zhu, X. Glycemic extremes are related to cognitive dysfunction in children with type 1 diabetes: A meta-analysis. J. Diabetes Investig. 2018, 9, 1342–1353. [Google Scholar] [CrossRef]
  32. Buchberger, B.; Huppertz, H.; Krabbe, L.; Lux, B.; Mattivi, J.T.; Siafarikas, A. Symptoms of depression and anxiety in youth with type 1 diabetes: A systematic review and meta-analysis. Psychoneuroendocrinology 2016, 70, 70–84. [Google Scholar] [CrossRef]
  33. Mommersteeg, P.M.C.; Herr, R.; Pouwer, F.; Holt, R.I.G.; Loerbroks, A. The association between diabetes and an episode of depressive symptoms in the 2002 World Health Survey: An analysis of 231,797 individuals from 47 countries. Diabet. Med. 2013, 30, e208–e214. [Google Scholar] [CrossRef]
  34. Heslop, P.; Blair, P.S.; Fleming, P.; Hoghton, M.; Marriott, A.; Russ, L. The Confidential Inquiry into premature deaths of people with intellectual disabilities in the UK: A population-based study. Lancet 2014, 383, 889–895. [Google Scholar] [CrossRef] [Green Version]
  35. Hendrieckx, C.; Ivory, N.; Singh, H.; Frier, B.M.; Speight, J. Impact of severe hypoglycaemia on psychological outcomes in adults with Type 2 diabetes: A systematic review. Diabet. Med. 2019, 36, 1082–1091. [Google Scholar] [CrossRef]
  36. Vanstone, M.; Rewegan, A.; Brundisini, F.; Dejean, D.; Giacomini, M. Patient Perspectives on Quality of Life With Uncontrolled Type 1 Diabetes Mellitus: A Systematic Review and Qualitative Meta-synthesis. Ont. Health Technol. Assess. Ser. 2015, 15, 1–29. [Google Scholar]
  37. Dalsgaard, E.-M.; Vestergaard, M.; Skriver, M.V.; Maindal, H.T.; Lauritzen, T.; Borch-Johnsen, K.; Witte, D.; Sandbaek, A. Psychological distress, cardiovascular complications and mortality among people with screen-detected type 2 diabetes: Follow-up of the ADDITION-Denmark trial. Diabetologia 2014, 57, 710–717. [Google Scholar] [CrossRef] [PubMed]
  38. Bartoli, F.; Carrà, G.; Crocamo, C.; Carretta, D.; La Tegola, D.; Tabacchi, T.; Gamba, P.; Clerici, M. Association between depression and neuropathy in people with type 2 diabetes: A meta-analysis. Int. J. Geriatr. Psychiatry 2016, 31, 829–836. [Google Scholar] [CrossRef] [PubMed]
  39. Lin, K.; Park, C.; Li, M.; Wang, X.; Li, X.; Li, W.; Quinn, L. Effects of depression, diabetes distress, diabetes self-efficacy, and diabetes self-management on glycemic control among Chinese population with type 2 diabetes mellitus. Diabetes Res. Clin. Pract. 2017, 131, 179–186. [Google Scholar] [CrossRef]
  40. World Health Organization. Cardiovascular Disease. Fact Sheets. 2017. Available online: https://www.who.int/en/news-room/fact-sheets/detail/cardiovascular-diseases-(cvds) (accessed on 22 May 2021).
  41. Jowett, N.; Cabot, L. Patients with cardiac disease: Considerations for the dental practitioner. Br. Dent. J. 2000, 189, 297–302. [Google Scholar] [CrossRef]
  42. Liu, M.-Y.; Li, N.; Li, W.A.; Khan, H. Association between psychosocial stress and hypertension: A systematic review and meta-analysis. Neurol. Res. 2017, 39, 573–580. [Google Scholar] [CrossRef] [PubMed]
  43. Wu, Y.; Sun, D.; Wang, B.; Li, Y.; Ma, Y. The relationship of depressive symptoms and functional and structural markers of subclinical atherosclerosis: A systematic review and meta-analysis. Eur. J. Prev. Cardiol. 2018, 25, 706–716. [Google Scholar] [CrossRef] [PubMed]
  44. Sokoreli, I.; de Vries, J.J.G.; Pauws, S.C.; Steyerberg, E.W. Depression and anxiety as predictors of mortality among heart failure patients: Systematic review and meta-analysis. Heart Fail. Rev. 2016, 21, 49–63. [Google Scholar] [CrossRef] [PubMed]
  45. Li, Z.; Li, Y.; Chen, L.; Chen, P.; Hu, Y. Prevalence of Depression in Patients with Hypertension. Med. (Baltim.) 2015, 94, e1317. [Google Scholar] [CrossRef]
  46. Crawshaw, J.; Auyeung, V.; Norton, S.; Weinman, J. Identifying psychosocial predictors of medication non-adherence following acute coronary syndrome: A systematic review and meta-analysis. J. Psychosom. Res. 2016, 90, 10–32. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Cannon, J.A.; Moffitt, P.; Perez-Moreno, A.C.; Walters, M.R.; Broomfield, N.M.; McMurray, J.J.V.; Quinn, T.J. Cognitive Impairment and Heart Failure: Systematic Review and Meta-Analysis. J. Card. Fail. 2017, 23, 464–475. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Easton, K.; Coventry, P.; Lovell, K.; Carter, L.-A.; Deaton, C. Prevalence and Measurement of Anxiety in Samples of Patients with Heart Failure. J. Cardiovasc. Nurs. 2016, 31, 367–379. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Brostow, D.P.; Petrik, M.L.; Starosta, A.J.; Waldo, S.W. Depression in patients with peripheral arterial disease: A systematic review. Eur. J. Cardiovasc. Nurs. 2017, 16, 181–193. [Google Scholar] [CrossRef] [PubMed]
  50. Vilchinsky, N.; Ginzburg, K.; Fait, K.; Foa, E.B. Cardiac-disease-induced PTSD (CDI-PTSD): A systematic review. Clin. Psychol. Rev. 2017, 55, 92–106. [Google Scholar] [CrossRef]
  51. Tully, P.J.; Turnbull, D.A.; Beltrame, J.; Horowitz, J.; Cosh, S.; Baumeister, H.; Wittert, G.A. Panic disorder and incident coronary heart disease: A systematic review and meta-regression in 1,131,612 persons and 58,111 cardiac events. Psychol. Med. 2015, 45, 2909–2920. [Google Scholar] [CrossRef]
  52. Valtorta, N.K.; Kanaan, M.; Gilbody, S.; Ronzi, S.; Hanratty, B. Loneliness and social isolation as risk factors for coronary heart disease and stroke: Systematic review and meta-analysis of longitudinal observational studies. Heart 2016, 102, 1009–1016. [Google Scholar] [CrossRef] [Green Version]
  53. Celano, C.M.; Millstein, R.A.; Bedoya, C.A.; Healy, B.C.; Roest, A.M.; Huffman, J.C. Association between anxiety and mortality in patients with coronary artery disease: A meta-analysis. Am. Heart J. 2015, 170, 1105–1115. [Google Scholar] [CrossRef] [Green Version]
  54. Buckland, S.A.; Pozehl, B.; Yates, B. Depressive Symptoms in Women with Coronary Heart Disease. J. Cardiovasc. Nurs. 2019, 34, 52–59. [Google Scholar] [CrossRef]
  55. Kendler, K.S.; Gardner, C.O.; Fiske, A.; Gatz, M. Major Depression and Coronary Artery Disease in the Swedish Twin Registry. Arch. Gen. Psychiatry 2009, 66, 857. [Google Scholar] [CrossRef]
  56. Gathright, E.C.; Goldstein, C.M.; Josephson, R.A.; Hughes, J.W. Depression increases the risk of mortality in patients with heart failure: A meta-analysis. J. Psychosom. Res. 2017, 94, 82–89. [Google Scholar] [CrossRef] [Green Version]
  57. Jonas, B.S.; Lando, J.F. Negative Affect as a Prospective Risk Factor for Hypertension. Psychosom. Med. 2000, 62, 188–196. [Google Scholar] [CrossRef] [Green Version]
  58. Mahmood, S.; Hassan, S.Z.; Tabraze, M.; Khan, M.O.; Javed, I.; Ahmed, A.; Siddiqui, O.M.; Narmeen, M.; Ahmed, M.J.; Tariq, A.; et al. Prevalence and Predictors of Depression Amongst Hypertensive Individuals in Karachi, Pakistan. Cureus 2017, 9, e1397. [Google Scholar] [CrossRef] [Green Version]
  59. Suzuki, S.; Kasanuki, H. The influences of psychosocial aspects and anxiety symptoms on quality of life of patients with arrhythmia: Investigation in paroxysmal atrial fibrillation. Int. J. Behav. Med. 2004, 11, 104–109. [Google Scholar] [CrossRef]
  60. Sears, S.F. Quality of life and psychological functioning of ICD patients. Heart 2002, 87, 488–493. [Google Scholar] [CrossRef] [Green Version]
  61. Addicks, S.H.; McNeil, D.W.; Randall, C.L.; Goddard, A.; Romito, L.M.; Sirbu, C.; Kaushal, G.; Metzger, A.; Weaver, B.D. Dental Care–Related Fear and Anxiety: Distress Tolerance as a Possible Mechanism. JDR Clin. Transl. Res. 2017, 2, 304–311. [Google Scholar] [CrossRef] [Green Version]
  62. Mills, R.; McCusker, C.G.; Tennyson, C.; Hanna, D. Neuropsychological outcomes in CHD beyond childhood: A meta-analysis. Cardiol. Young 2018, 28, 421–431. [Google Scholar] [CrossRef]
  63. Luyckx, V.A.; Tonelli, M.; Stanifer, J.W. The Global Burden of Kidney Disease and the Sustainable Development Goals; Bulletin of the World Health Organization: Geneva, Switzerland, 2018; Volume 96. [Google Scholar]
  64. Costantinides, F.; Castronovo, G.; Vettori, E.; Frattini, C.; Artero, M.L.; Bevilacqua, L.; Berton, F.; Nicolin, V.; Di Lenarda, R. Dental Care for Patients with End-Stage Renal Disease and Undergoing Hemodialysis. Int. J. Dent. 2018, 9610892. [Google Scholar] [CrossRef]
  65. de Rossi, S.S.; Glick, M. Dental considerations for the patient with renal disease receiving hemodialysis. J. Am. Dent. Assoc. 1996, 127, 211–219. [Google Scholar] [CrossRef]
  66. Kim, J.C.; Kalantar-Zadeh, K.; Kopple, J.D. Frailty and Protein-Energy Wasting in Elderly Patients with End Stage Kidney Disease. J. Am. Soc. Nephrol. 2013, 24, 337–351. [Google Scholar] [CrossRef] [Green Version]
  67. Levy, N.B. What is psychonephrology? J. Nephrol. 2008, 21 (Suppl. 1), S51–S53. [Google Scholar]
  68. Ravaghi, H.; Behzadifar, M.; Behzadifar, M.; Taheri Mirghaed, M.; Aryankhesal, A.; Salemi, M.; Bragazzi, N.L. Prevalence of Depression in Hemodialysis Patients in Iran: A Systematic Review and Meta-analysis. Iran. J. Kidney Dis. 2017, 11, 90–98. [Google Scholar]
  69. Muscat, P.; Chilcot, J.; Weinman, J.; Hudson, J. Exploring the relationship between illness perceptions and depression in patients with chronic kidney disease: A systematic literature review. J. Ren. Care 2018, 44, 174–185. [Google Scholar] [CrossRef]
  70. Gregg, L.P.; Carmody, T.; Le, D.; Martins, G.; Trivedi, M.; Hedayati, S.S. A Systematic Review and Meta-Analysis of Depression and Protein–Energy Wasting in Kidney Disease. Kidney Int. Rep. 2020, 5, 318–330. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. De Pasquale, C.; Pistorio, M.L.; Veroux, M.; Indelicato, L.; Biffa, G.; Bennardi, N.; Zoncheddu, P.; Martinelli, V.; Giaquinta, A.; Veroux, P. Psychological and Psychopathological Aspects of Kidney Transplantation: A Systematic Review. Front. Psychiatry 2020, 11. [Google Scholar] [CrossRef] [Green Version]
  72. Berger, I.; Wu, S.; Masson, P.; Kelly, P.J.; Duthie, F.A.; Whiteley, W.; Parker, D.; Gillespie, D.; Webster, A.C. Cognition in chronic kidney disease: A systematic review and meta-analysis. BMC Med. 2016, 14, 206. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Shea, Y.; Lee, M.C.; Mok, M.M.; Chan, F.H.; Chan, T.M. Prevalence of cognitive impairment among peritoneal dialysis patients: A systematic review and meta-analysis. Clin. Exp. Nephrol. 2019, 23, 1221–1234. [Google Scholar] [CrossRef] [PubMed]
  74. Bailey, P.K.; Hamilton, A.J.; Clissold, R.L.; Inward, C.D.; Caskey, F.J.; Ben-Shlomo, Y.; Owen-Smith, A. Young adults’ perspectives on living with kidney failure: A systematic review and thematic synthesis of qualitative studies. BMJ Open 2018, 8, e019926. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Sousa, H.; Ribeiro, O.; Paúl, C.; Costa, E.; Miranda, V.; Ribeiro, F.; Figueiredo, D. Social support and treatment adherence in patients with end-stage renal disease: A systematic review. Semin. Dial. 2019, 32, 562–574. [Google Scholar] [CrossRef]
  76. Tanaka, M.; Yamazaki, S.; Hayashino, Y.; Fukuhara, S.; Akiba, T.; Saito, A.; Asano, Y.; Port, F.K.; Kurokawa, K.; Akizawa, T. Hypercalcaemia is associated with poor mental health in haemodialysis patients: Results from Japan DOPPS. Nephrol. Dial. Transplant. 2007, 22, 1658–1664. [Google Scholar] [CrossRef] [Green Version]
  77. Celano, C.M.; Freudenreich, O.; Fernandez-Robles, C.; Stern, T.A.; Caro, M.A.; Huffman, J.C. Depressogenic effects of medications: A review. Dialogues Clin. Neurosci. 2011, 13, 109–125. [Google Scholar] [CrossRef]
  78. Borda, M.G.; Soennesyn, H.; Steves, C.J.; Osland Vik-Mo, A.; Pérez-Zepeda, M.U.; Aarsland, D. Frailty in Older Adults with Mild Dementia: Dementia with Lewy Bodies and Alzheimer’s Disease. Dement. Geriatr. Cogn. Dis. Extra 2019, 9, 176–183. [Google Scholar] [CrossRef]
  79. Xiao, J.L.; Xu, G.C.; de Hoog, S.; Qiao, J.J.; Fang, H.; Li, Y.L. Oral Prevalence of Candida Species in Patients Undergoing Systemic Glucocorticoid Therapy and the Antifungal Sensitivity of the Isolates. Infect Drug Resist. 2020, 13, 2601–2607. [Google Scholar] [CrossRef]
  80. Cheng, T.; Li, Y.; Zhang, H.; Chen, L.; Tu, J.; Hui, X.; Cheng, Q.; Wan, H. Incidence of oral candidiasis is associated with inhaled corticosteroids in Chinese patients: A systematic review and meta-analysis. Int. J. Clin. Exp. Med. 2017, 10, 5546–5560. [Google Scholar]
  81. Nadig, S.; Ashwathappa, D.; Manjunath, M.; Krishna, S.; Annaji, A.; Shivaprakash, P. A relationship between salivary flow rates and Candida counts in patients with xerostomia. J. Oral Maxillofac. Pathol. 2017, 21, 316. [Google Scholar] [CrossRef] [Green Version]
  82. Louati, K.; Berenbaum, F. Fatigue in chronic inflammation—A link to pain pathways. Arthritis Res. Ther. 2015, 17, 254. [Google Scholar] [CrossRef] [Green Version]
  83. Qiu, X.; Zhang, X.; Cai, L.; Yan, C.; Yu, L.; Fan, J.; Zhang, R.; Huang, J.; Duan, X. Rheumatoid arthritis and risk of anxiety: A meta-analysis of cohort studies. Clin. Rheumatol. 2019, 38, 2053–2061. [Google Scholar] [CrossRef]
  84. Basta, F.; Afeltra, A.; Margiotta, D.P.E. Fatigue in systemic sclerosis: A systematic review. Clin. Exp. Rheumatol. 2018, 36 (Suppl. 1), 150–160. [Google Scholar]
  85. Primdahl, J.; Hegelund, A.; Lorenzen, A.G.; Loeppenthin, K.; Dures, E.; Appel Esbensen, B. The Experience of people with rheumatoid arthritis living with fatigue: A qualitative metasynthesis. BMJ Open 2019, 9, e024338. [Google Scholar] [CrossRef]
  86. Matcham, F.; Ali, S.; Hotopf, M.; Chalder, T. Psychological correlates of fatigue in rheumatoid arthritis: A systematic review. Clin. Psychol. Rev. 2015, 39, 16–29. [Google Scholar] [CrossRef] [Green Version]
  87. Gu, M.; Cheng, Q.; Wang, X.; Yuan, F.; Sam, N.; Pan, H.; Li, B.; Ye, D. The impact of SLE on health-related quality of life assessed with SF-36: A systemic review and meta-analysis. Lupus 2019, 28, 371–382. [Google Scholar] [CrossRef] [PubMed]
  88. Al-Ezzi, M.Y.; Pathak, N.; Tappuni, A.R.; Khan, K.S. Primary Sjögren’s syndrome impact on smell, taste, sexuality and quality of life in female patients: A systematic review and meta-analysis. Mod. Rheumatol. 2017, 27, 623–629. [Google Scholar] [CrossRef]
  89. Smirani, R.; Truchetet, M.; Poursac, N.; Naveau, A.; Schaeverbeke, T.; Devillard, R. Impact of systemic sclerosis oral manifestations on patients’ health-related quality of life: A systematic review. J. Oral Pathol. Med. 2018, 47, 808–815. [Google Scholar] [CrossRef] [PubMed]
  90. Meade, T.; Manolios, N.; Cumming, S.R.; Conaghan, P.G.; Katz, P. Cognitive Impairment in Rheumatoid Arthritis: A Systematic Review. Arthritis Care Res. (Hoboken) 2018, 70, 39–52. [Google Scholar] [CrossRef] [PubMed]
  91. Li, Z.; Yang, Y.; Dong, C.; Li, L.; Cui, Y.; Zhao, Q.; Gu, Z. The prevalence of suicidal ideation and suicide attempt in patients with rheumatic diseases: A systematic review and meta-analysis. Psychol. Health Med. 2018, 23, 1025–1036. [Google Scholar] [CrossRef]
  92. Nerurkar, L.; Siebert, S.; McInnes, I.B.; Cavanagh, J. Rheumatoid arthritis and depression: An inflammatory perspective. The Lancet Psychiatry 2019, 6, 164–173. [Google Scholar] [CrossRef]
  93. Hanly, J.G. Diagnosis and management of neuropsychiatric SLE. Nat. Rev. Rheumatol. 2014, 10, 338–347. [Google Scholar] [CrossRef]
  94. de Almeida Macêdo, E.; Appenzeller, S.; Lavras Costallat, L.T. Assessment of the Hospital Anxiety and Depression Scale (HADS) performance for the diagnosis of anxiety in patients with systemic lupus erythematosus. Rheumatol. Int. 2017, 37, 1999–2004. [Google Scholar] [CrossRef]
  95. Cui, Y.; Li, L.; Yin, R.; Zhao, Q.; Chen, S.; Zhang, Q.; Shen, B. Depression in primary Sjögren’s syndrome: A systematic review and meta-analysis. Psychol. Health Med. 2018, 23, 198–209. [Google Scholar] [CrossRef]
  96. Chau, S.Y.; Mok, C.C. Factors predictive of corticosteroid psychosis in patients with systemic lupus erythematosus. Neurology 2003, 61, 104–107. [Google Scholar] [CrossRef]
  97. Bhangle, S.D.; Kramer, N.; Rosenstein, E.D. Corticosteroid-induced neuropsychiatric disorders: Review and contrast with neuropsychiatric lupus. Rheumatol. Int. 2013, 33, 1923–1932. [Google Scholar] [CrossRef]
  98. Koray, M.; Dülger, O.; Ak, G.; Horasanli, S.; Uçok, A.; Tanyeri, H.; Badur, S. The evaluation of anxiety and salivary cortisol levels in patients with oral lichen planus. Oral Dis. 2003, 9, 298–301. [Google Scholar] [CrossRef]
  99. Toyofuku, A. Psychosomatic problems in dentistry. BioPsychoSocial Med. 2016, 10, 14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Rivera, C. Essentials of recurrent aphthous stomatitis. Biomed Rep. 2019, 11, 47–50. [Google Scholar] [CrossRef] [Green Version]
  101. Reners, M.; Brecx, M. Stress and periodontal disease. Int. J. Dent. Hyg. 2007, 5, 199–204. [Google Scholar] [CrossRef] [PubMed]
  102. Tikhonova, S.; Booij, L.; D’Souza, V.; Crosara, K.T.B.; Siqueira, W.L.; Emami, E. Investigating the association between stress, saliva and dental caries: A scoping review. BMC Oral Health 2018, 18, 41. [Google Scholar] [CrossRef] [Green Version]
  103. da Silva, A.N.; de Lima, S.T.A.; Vettore, M.V. Protective psychosocial factors and dental caries in children and adolescents: A systematic review and meta-analysis. Int. J. Paediatr. Dent. 2018. [Google Scholar] [CrossRef] [PubMed]
  104. Kisely, S.; Sawyer, E.; Siskind, D.; Lalloo, R. The oral health of people with anxiety and depressive disorders—A systematic review and meta-analysis. J. Affect Disord. 2016, 200, 119–132. [Google Scholar] [CrossRef] [PubMed]
Table 1. Psychological background of patients with diabetes.
Table 1. Psychological background of patients with diabetes.
References
A.Poor quality of life
Depression, anxiety, and worry in diabetes is associated with poor quality of life [OR = 3.0 (95% CI: 1.135–7.948)][19]
B.Diabetes as a risk factor for psychological problems
Patients with diabetes have an increased risk of developing anxiety (OR = 1.48 (95% CI: 1.27–1.74)) and depressive symptoms (RR = 1.29 (95% CI: 1.03–1.63))[4,26]
Diabetic distress is present in about one-third of type 1 and type 2 diabetes mellitus patients[3,18]
Depression, anxiety, low quality of life, and poor sleep are associated with painful diabetic neuropathy[21]
C.Diabetes with depression leading to other complications
Patients with diabetes and depression have poorer cognitive function compared to those with diabetes alone[22]
Patients with diabetes and depression have an increased risk of microvascular (retinopathy, neuropathy) ((HR = 1.38 (95% CI: 1.30–1.47)) and macrovascular complications (stroke, angina, cardiovascular diseases) ((HR = 1.33 (95% CI: 1.25–1.41))[23]
D.Diabetes as a risk factor for suicide
Patients with diabetes have an increased risk of suicide (RR  =  1.56; (95% CI: 1.29–1.89))[24]
E.Poor cognition
Diabetes in children and adults is associated with cognitive dysfunction such as lowered intelligence, diminished attention, and slowing of psychomotor speed[20,25,27,28]
F.Anxiety/Stress as a risk factor for diabetes
Anxiety might be a risk factor for diabetes (OR = 1.47 (95% CI: 1.23–1.75))[29]
Women are associated with work-related stress and risk of diabetes (RR = 1.22 (95% CI: 1.01–1.46))[30]
Workplace bullying victims had 1.46 times higher risk of developing diabetes compared to those who had not experienced workplace bullying (HR = 1.46 (95% CI: 1.23–1.74))[31]
Table 2. Psychological backgrounds of patients with cardiovascular diseases.
Table 2. Psychological backgrounds of patients with cardiovascular diseases.
References
A.Anxiety and depression in cardiovascular patients
Prevalence of anxiety in heart failure: anxiety disorders (13.1%), clinically significant anxiety (28.7%), and elevated symptoms of anxiety (55.5%)
Prevalence of depression in peripheral arterial disease: 3% to 48% prevalence of depression in myocardial infarction: female (36%), male (29%)
[5,44,45]
B.Post-traumatic Stress Disorder (PTSD)
Prevalence of cardiac disease-induced PTSD averaged 12%[46]
C.Panic Disorders
Panic disorder is associated with incident coronary heart disease (HR = 1.47 (95% CI: 1.25–1.74)) and myocardial infarction (HR = 1.36 (95% CI: 1.45–1.85))[47]
D.Loneliness and social isolation
Poor social relationships are associated with a 29% increase in the risk of incident coronary heart disease[48]
E.Anxiety and depression as a risk of mortality
Anxiety and depression are associated with an increased risk of mortality in patients with coronary artery disease (OR = 1.21 (95% CI:1.06–1.39)) and heart failure (HR = 1.57 (95 %CI: 1.30–1.89)), respectively[49,50]
F.Cardiovascular diseases and depression leading to decreased treatment compliance
Depression in hypertensive patients and acute coronary syndrome patients associated with decreased treatment compliance (Prevalence-26.8%) and non-adherence to medication (OR = 2.00 (95% CI: 1.57–3.33)), respectively[51,52]
G.Poor cognition
Prevalence of cognitive impairment in heart failure patients averaged 43% (OR = 1.67 (95% CI: 1.15–2.42))[53]
H.Stress/depression symptoms as a risk factor for cardiovascular diseases
Psychosocial stress such as occupational stress, socioeconomic status, anxiety, and depression are associated with an increased risk of hypertension (OR = 2.40 (95% CI = 1.65–3.49))[42]
Depressive symptoms contributed to subclinical atherosclerosis with impaired functional and structural markers[43]
Table 3. Psychological backgrounds of patients with renal diseases.
Table 3. Psychological backgrounds of patients with renal diseases.
References
A.Anxiety, Distress, and Depression
Depression is one of the most prevalent mental illnesses (ranging from 6–83.5% among studies) in hemodialysis patients.[7,68]
Chronic Kidney Disease (CKD) patients have negative emotions and distress. Disease severity and illness perception is associated with depression[69]
Low albumin, high Interlukin-6, and high C-Reactive Protein are associated with the severity of depressive symptoms in chronic renal disease[70]
Kidney transplant patients are exposed to a high risk of psychiatric disorders such as mental distress, behavioral and adaptation difficulties, cognitive impairments and depressive symptoms, sleep disorders, anxiety, and depression[71]
B.Post-Traumatic Stress Disorder (PTSD)
PTSD is common in patients with solid organ transplants, including renal transplant[8]
C.Effect on cognition
Renal patients experienceeffects on orientation and attention, language, concept formation and reasoning, executive function, memory, and global cognition. The cognitive impact might diminish the patient’s ability to make health care decisions[72]
The pooled prevalence of cognitive impairment among peritoneal dialysis patients is 28.7%[73]
D.Effect on quality of life
Renal failure is associated with lower quality of life in young adults[74]
E.Need for social support
A significant association between social support and treatment adherence is seen in patients with end-stage renal disease.[75]
Table 4. Psychological backgrounds of patients with connective tissue diseases.
Table 4. Psychological backgrounds of patients with connective tissue diseases.
References
A.Anxiety and depression
The depressive (6.7% to 59%) and anxiety symptoms (34% to 37%) are prevalent in childhood-onset systemic lupus erythematosus (SLE)[9]
Patients with rheumatoid arthritis are associated with an increased risk of anxiety OR = 1.20 (95% CI: 1.03–1.39)[83]
B.Fatigue in connective tissue diseases and its psychosocial factors
Fatigue in SLE is associated with psychosocial factors (depression, pain, and sleep disorders)[84]
The dominant unpredictability of rheumatoid arthritis-related fatigue is experienced as a vicious circle described in relation to its physical, cognitive, emotional, and social impact[85]
Low mood is associated with increased fatigue in rheumatoid arthritis patients[86]
C.Poor quality of life
SLE has a significant impact on the health-related quality of life (Mental component summary = 50.37 (95% CI: 47.78–52.87))[87]
Primary Sjögren’s syndrome has an impact on quality of life in female patients (mental component of the quality of life = −0.83 (95% CI: −1.27 to −0.40))[88]
There is a significant association between the oropharyngeal manifestations of systemic sclerosis (assessed as maximal mouth opening and mouth handicap in systemic sclerosis scale) and impaired quality of life[89]
D.Poor cognitive function
A significant underperformance in cognitive function tests, mainly verbal functions, memory, and attention in rheumatoid arthritis patients is observed when compared to controls[90]
E.Suicide ideation and attempt
Rheumatic diseases patients have a high pooled prevalence of suicidal ideation (26%) and suicide attempts (12%). The prevalence of suicidal ideation and a suicidal attempts is higher in females than in males[91]
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Abiko, Y.; Paudel, D.; Matsuoka, H.; Moriya, M.; Toyofuku, A. Psychological Backgrounds of Medically Compromised Patients and Its Implication in Dentistry: A Narrative Review. Int. J. Environ. Res. Public Health 2021, 18, 8792. https://doi.org/10.3390/ijerph18168792

AMA Style

Abiko Y, Paudel D, Matsuoka H, Moriya M, Toyofuku A. Psychological Backgrounds of Medically Compromised Patients and Its Implication in Dentistry: A Narrative Review. International Journal of Environmental Research and Public Health. 2021; 18(16):8792. https://doi.org/10.3390/ijerph18168792

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Abiko, Yoshihiro, Durga Paudel, Hirofumi Matsuoka, Mitsuru Moriya, and Akira Toyofuku. 2021. "Psychological Backgrounds of Medically Compromised Patients and Its Implication in Dentistry: A Narrative Review" International Journal of Environmental Research and Public Health 18, no. 16: 8792. https://doi.org/10.3390/ijerph18168792

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