Abstract
Androgenetic alopecia is the most common form of hair loss, affecting 85% of men and 40% of women. Androgenetic alopecia is a disease caused by multiple factors, such as genetics, hormones, and systemic diseases; however, the exact cause remains undetermined. Recent studies have found that it is associated with a high incidence of endocrine diseases and other comorbidities. It may not only be a skin disease but also an early signal of underlying systemic diseases. Effective management requires timely diagnosis and treatment initiation. However, in current clinical practice, androgenetic alopecia is still not fully understood or treated. Recognizing the true physical, social, and emotional burden of androgenic alopecia, as well as its associated comorbidities, is the first step in improving the prognosis of affected patients. This review aimed to gather the known pathological factors and provide a reference for clinical physicians to understand androgenetic alopecia and its comorbidities in depth, thereby enabling early recognition of the underlying systemic diseases and providing timely treatment.
Similar content being viewed by others
Androgenetic alopecia is a multifactorial disease that seriously affects people’s work, love, and interpersonal relationships. At present, its specific pathogenesis is still elusive, and the existing treatment cannot give satisfactory results to patients. |
We reviewed recent studies on the systemic diseases associated with androgenetic alopecia. |
It is hoped that our research will lead to a better understanding that this disease is not a simple skin disease, as well as early diagnosis and treatment of other diseases to improve patient outcomes. |
Introduction
In modern society, hair is an important part of one’s self-image. Therefore, hair loss brings many troubles to people, such as impaired image, impacted self-confidence, failure of a marriage, and love, and may impact people's health. Studies have shown that hair loss can cause various psychological difficulties, such as anxiety, depression, and trauma, and further impair quality of life (QoL) [1,2,3]. Androgenetic alopecia (AGA), commonly known as male or female pattern baldness, is the most common progressive hair loss disorder [4]. Although studies have reported that androgens and their receptors, gene expression patterns, inflammation mediators, signaling pathways, and disorders might be related to the occurrence of AGA, the etiology and pathogenesis of AGA still require further investigation [5,6,7], which might provide novel targets for prevention and therapy. Dihydrotestosterone (DHT), a metabolite of testosterone, is regularly considered one of the key mediators of AGA. It acts on androgen receptors in hair follicles, thereby shortening the anagen (growth) phase and prolonging the telogen (resting) phase of hair growth, resulting in an increase in immature hair and a decrease in new hair [4, 8,9,10]. The current treatment plan for AGA mainly includes oral finasteride, topical external use of minoxidil, low-intensity laser, hair transplantation, etc. Finasteride is a 5α-reductase inhibitor that has a significant effect on the treatment of AGA; however, it can also exhibit unacceptable side effects in a small subset of patients. Occasionally, side effects persist even after treatment cessation in the form of the post-finasteride syndrome [11]. Minoxidil effectively inhibits the hair loss process; however, once the drug is discontinued, hair from minoxidil-mediated hair growth begins to fall out. Therefore, patients must use it indefinitely and persistently to maintain efficacy [12]. Additionally, minoxidil can cause undesirable adverse effects. Currently, low-intensity laser therapy has shown promising results in the treatment of AGA; however, the effectiveness of its treatment remains controversial [5].
The presence of a chronic disorder that co-occurs, simultaneously or in tandem, with a primary disease is comorbidity [13]. Comorbidities can aggravate patients’ physical and mental sufferings. For physicians, comorbidities pose new challenges for diagnosis and treatment. Some researchers have pointed out that AGA is associated with systemic diseases such as metabolic syndrome, endocrine diseases, and mental disorders [1, 14,15,16,17]. Previous studies have discussed the relationship between alopecia areata and systemic diseases [18,19,20] (Table 1). However, to the best of our knowledge, few studies have discussed the relationship between AGA and other systemic diseases. Timely diagnosis and treatment of these potential systemic diseases are extremely important for the management and improvement of AGA. The more accurate our understanding of AGA and its comorbidities, the better the clinical diagnosis and treatment can be. Here, we review the current insights into the pathology and relationships between AGA and systemic diseases and seek novel and potential avenues for its diagnosis and treatment to help patients with AGA. This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.
Endocrine Disease
The growth, circulation, and density of hair are mainly regulated by circulating hormones. Thus, endocrine system diseases are often accompanied by hair loss [21]. Hyperandrogenemia (HA) refers to a condition in which the ovaries and adrenal cortex secrete excessive testosterone. One of the common androgenic skin changes is androgenic alopecia [22]. The earliest suspected relationship between HA and AGA can be traced back to the Renaissance period and the 18th century [23]. A study reviewed other skin manifestations in women with high androgen levels and found that AGA is a common clinical manifestation but cannot be used as a useful clinical marker [24]. In a report of a 63-year-old woman with hirsutism and alopecia, her experimental data emphasized an increase in androgen levels [25]. For postmenopausal women with hirsutism and AGA, to achieve a better therapeutic effect, we must find the cause of elevated androgen levels, such as the source of a tumor [26, 27]. Nevertheless, most studies have shown that AGA is not yet a sign of HA [24, 27,28,29]. Many studies have discussed female androgen excess, but recently, a cross-sectional study of male HA has been conducted. A study of 100 men with elevated androgen levels found that patients with elevated DHT levels had a higher frequency of hair loss [30]. These studies continue to prove that patients with HA are more prone to AGA. However, the existing evidence generally shows that the androgen level in the blood circulation of patients with AGA is maintained at a normal level. The association between HA and AGA may not be attributable to increased levels of androgens in the blood. Apart from androgens, what else exists between them?
HA does not appear alone and is often one of the manifestations of other diseases. It mainly originates from ovarian and adrenal diseases and other rare causes, such as local androgen abnormalities in target organs, drugs using exogenous androgens, and hyperprolactinemia. We speculated that AGA and HA may be common manifestations of ovarian and adrenal diseases. HA occurs most often in patients with polycystic ovary syndrome (PCOS). In a prospective study of patients with PCOS, the prevalence of AGA was 30% [31]. However, this study involved 20 patients with PCOS. In an Anahita Jalilian meta-analysis of Iranian women with PCOS and its comorbidities, the prevalence of AGA was estimated to be 9% [32]. In the Molly Quinn study, 56 PCOS patients had AGA (22.0%) [29]. The difference in prevalence might be attributed to different population groups, as well as different screening methods used to diagnose PCOS. Feng et al. also agreed that AGA was a common dermatological manifestation in women with PCOS and those without. There were no significant differences in the age of patients with PCOS between the AGA and non-AGA groups (P = 0.453) [28]. Based on the autosomal genetic transmission of PCOS and symptoms of PCOS in men of families where women are often affected by PCOS, researchers have proposed the existence of a male equivalent of PCOS [33, 34]. A cross-sectional study in Taiwan, China, showed that overweight women with PCOS are at a significantly higher risk of female pattern hair loss (FPHL). This study also showed that there may be ethnic differences in the susceptibility of patients with PCOS to the development of FPHL [35]. However, Molly Quinn’s study concluded that there was no significant difference in the incidence of AGA between White participants and non-White participants (21.8 vs. 21.1%; P = 0.91) [29]. In contrast, Timothy and Schmidt had different results. Their cross-sectional study aimed to determine the skin and body characteristics of patients with PCOS to help diagnose PCOS. They found that women who met the PCOS criteria had an increased prevalence of AGA than those who did not, but this difference was not statistically significant (22.4% [53 of 237] vs. 11.4% [5 of 44], P = 0.10) [36]. In general, patients with PCOS are more likely to develop AGA. However, there is still insufficient evidence to explain this. We believe that, to some extent, this is related to heredity, weight, and gender. To the best of our knowledge, no study has found an association between adrenal gland disease and AGA.
AGA, acanthosis nigricans, and PCOS are recognized as early clinical manifestations of insulin resistance, and these manifestations represent the risk of further developing type 2 diabetes [37]. A study directly elucidated that diabetes was significantly associated with FPHL frontal alopecia (P = 0.023) [38]. Insulin resistance might induce a hormonal imbalance in circulating androgens, which may explain the relationship between diabetes and AGA [39]. A prospective study in Taiwan concluded that moderate-to-severe AGA was an independent predictor of diabetes [40]. However, another study did not show any significant association between type 2 diabetes and AGA [41]. It is well known that the main bridge between AGA and diabetes is insulin resistance. Insulin resistance plays an important role in diabetes onset.
Baseline and stimulated thyroid-stimulating hormone levels were significantly increased in patients with AGA following thyrotropin-releasing hormone (TRH) stimulation [42]. According to the results of a study of 65 men with AGA (average age, 24 years) and 46 women with AGA, AGA in women was associated with hypothyroidism [43]. A retrospective study by Tee Wei Siah found that 12% (aged 24–73 years) of 210 patients with FPHL had a long-term history of hypothyroidism [44]. Babaei et al. suggested that if hair loss occurs early, there may be concomitant diseases such as hypothyroidism [45]. Patients with AGA may be accompanied by hypothyroidism. Unfortunately, there is insufficient evidence and low quality; however, this possibility must be considered.
Cancer
Recently, some scholars have proposed that AGA is also related to cancer, but the results of these studies are controversial [46,47,48,49,50,51]. A meta-analysis assessed the relationship between cancer incidence or cancer-specific mortality and AGA categories using retention odds ratios (OR) or hazard ratios (HR) with 95% confidence intervals (CI). A significant increase in risk was observed in relation to high-grade prostate cancer (PC) (OR 1.42; 95% CI 1.02–1.99), and vertex with/without frontal baldness was associated with PC risk. Nevertheless, using AGA as a phenotypic marker for PC risk was poorly supported [46]. Rokni et al. also showed that there is a significant relationship between PC and AGA. However, the association between these two diseases may be due to androgens [47]. Prostate-specific antigen (PSA) is a biomarker for PC. It has been approved by the US Food and Drug Administration as an aid for the early detection of PC [52]. However, in an AGA case–control study, there was no significant difference in the mean serum PSA levels between patients and controls [48]. Based on existing research, whether PC and AGA are related remains controversial. The pooled results of this meta-analysis also showed that AGA, especially frontal baldness, was associated with the incidence of testicular germ cell tumors (OR 0.69; 95% CI 0.58–0.83). However, the specific degree of baldness does not affect the incidence or specific mortality of cancer [46]. In addition, AGA is associated with androgen-secreting tumors. Wesolowska et al. reported a 64-year-old postmenopausal woman with an ovarian tumor who developed advanced AGA and progressive hirsutism within 3 years [49]. Ferrinho Catia et al. reported a similar case [51]. These reports indicate that increased androgen levels may lead to the appearance of AGA in androgen-secreting tumors. In addition, Taiwanese women with hair loss have a higher risk of thyroid cancer [50]. However, this study did not completely rule out other pathogenic factors that could lead to thyroid cancer. These positive results should be interpreted carefully because of the limitations of these studies.
Metabolic Disease
Metabolic syndrome (MetS) refers to the pathological state in which the body's proteins, fats, carbohydrates, and other substances are metabolically disordered. It is a complex metabolic syndrome and a risk factor for diabetic cardiovascular and cerebrovascular diseases. Over the past two decades, the relationship between AGA and MetS has been proven [53]. In a case and control study involving 100 AGA cases (20–50 years), MetS were observed in 53% of cases and 17% of controls (P = 0.001) [54]. Gopinath and Upadya conducted a hospital-based, analytical, cross-sectional study of 85 men with early onset AGA. The results showed that the MetS was observed in 19 (22.4%) patients with AGA and eight (9.4%) control groups (P = 0.021). Compared to the patients in the control group, those with AGA had significantly higher reductions in abdominal obesity, hypertension, and high-density lipoprotein. However, the subgroup of the study only had a small sample size and lacked evidence of a temporal relationship between MetS and AGA [55]. Another study showed that there were 37 (64.9%) and 29 (53.7%) patients with AGA in the case and control groups, respectively, and the difference was statistically significant (P < 0.0001) [56]. Only approximately 10% of the patients had MetS, although the difference was not statistically significant (P = 0.092). Compared with control group patients, those with AGA had significantly higher reductions in abdominal obesity, hypertension, and high-density lipoprotein levels [57]. A study by Ola Ahmed Bakry stated that MetS is more common in patients with AGA with severity of 12/40 (30%) than in 2/60 (3.3%) patients with mild-to-moderate severity. However, compared to patients with extremely severe AGA, those with mild to moderately severe AGA had a lesser tendency to develop metabolic conditions [58]. Most studies have unanimously concluded that there is some evidence linking AGA to MetS. However, there are insufficient studies on the correlation between AGA severity and MetS.
Cardiovascular Diseases
Cardiovascular diseases are a major cause of morbidity and mortality worldwide [59]. Several studies have reported an association between AGA and cardiovascular risk [60]. Amamoto Misato et al. screened a total of nine studies (eight on AGA, one alopecia areata: 44,806 participants) in the Medline and Embase databases for a meta-analysis and found that compared to men without baldness, those with AGA had an increased risk of heart disease, and younger men (< 55 years or ≤ 60 years) showed a stronger correlation [61]. Salvador Arias-Santiago confirmed the association between early onset AGA and a higher cardiovascular risk in men and women groups. They found that the prevalence of carotid atherosclerosis (atherosclerotic plaque) in patients with AGA was higher than that in the control group. Moreover, the prevalence of family history of cardiovascular disease in the men and women AGA groups was significantly higher than that in the control group [62]. Wang Ya-Xin’s research further found that AGA status (OR 2.247; 95% CI 1.396–3.617, P = 0.001), severe AGA (OR 2.360; 95% CI 1.506–3.699, P < 0.001), and early onset AGA (OR 3.54%; 95% CI 2.069–5.832, P < 0.001) were independently correlated with the severity of coronary atherosclerosis [63]. A meta-analysis revealed that the serum total cholesterol, triglycerides, and low-density lipoprotein cholesterol levels in the AGA group were significantly higher than those in the control group, and the standardized mean differences were 0.377 (95% CI 0.182–0.572, P < 0.001), 0.426 (95% CI 0.164–0.688, P = 0.001), and 0.450 (95% CI 0.171–0.728, P = 0.002), respectively [64], which further confirmed the results of previous studies. In a prospective case–control study in India, there were 468 confirmed cases of coronary artery disease (CAD) and 912 age-matched healthy men. The results showed that the prevalence of AGA (49.1 vs. 27.4%) was higher in the CAD group than in the control group. Multiple logistic regression analysis indicated that AGA [5.619, 95% CI 4.025–7.845, P < 0.0001] was the strongest predictor of CAD in young Asian men. This may indicate that AGA can be effectively used for the early prediction of CAD [65]. Several studies have investigated the association between AGA and hypertension. In addition, Serge Ahouansou claimed that hypertension and AGA are strongly related and that this association was independent of age [66]. In a case–control study, the aldosterone level and blood pressure of patients with AGA were significantly higher than those of the control group (P < 0.05) [67]. Women with early onset AGA have high systolic blood pressure, diastolic blood pressure, and aldosterone levels [68]. Unfortunately, Danesh-Shakiba et al. did not find a significant association between certain cardiovascular risk factors (e.g., hypertension and smoking) and AGA. Although patients with severe AGA have significantly higher systolic and diastolic blood pressures, their average age is also significantly higher [69]. Elevated aldosterone levels are considered the cause of AGA and high blood pressure. Existing evidence indicates that AGA is independently related to cardiovascular disease and may be an indicator for early prediction of cardiovascular disease in the future.
Mental Illnesses
Hair loss and subsequent beauty problems can adversely affect mental health. AGA is increasingly associated with social isolation, which leads to depression, anxiety, and loss of confidence [70,71,72,73]. Therefore, mental health problems are more common in patients with AGA than in healthy individuals. However, no systematic evaluation has been performed of the association between AGA and mental illness. Wang Xia et al. evaluated the psychological use of the SCL-90-R scale for AGA in 355 Chinese college students. There were significant differences in obsessive–compulsive disorder, depression, and phobic anxiety between college students with AGA and the control group [70]. A meta-analysis of the association between AGA and health-related quality of life (HRQOL) and mental illness (41 studies involving 7995 patients) found that AGA was significantly related to HRQOL and moderate emotional impairment, but not depressive symptoms. This meta-analysis also found that physician-rated hair loss severity is unrelated to HRQOL in AGA [71]. Tas Betul et al. evaluated self-awareness, self-esteem, sexual experience, and anxiety in 353 patients with AGA aged 15–63 years (men: 283 cases, women: 70 cases). They found that women had more serious psychological disorders than men [72]. Tabolli Stefano et al. also confirmed the high prevalence of depression/anxiety in patients with AGA, and the prevalence in women with AGA was significantly higher than that in men [73]. Except for depression and anxiety, the prevalence of AGA in patients with schizophrenia was significantly higher than in those without schizophrenia [74]. Because the hair loss assessment instrument and classification of severity in each evaluation tool varied among the included studies, which may have caused inconsistencies in the results of the above studies, the potential mechanism is worth investigating.
Urinary System Diseases
AGA, benign prostatic hyperplasia (BPH), and PC are androgen-dependent diseases. AGA and BPH have good therapeutic responses to finasteride [75, 76]. Therefore, we aimed to investigate the relationship between AGA and urinary system disease more closely. Interestingly, in a retrospective survey, the age, body mass index, hypertension, diabetes, baldness patterns, and serum T levels of 200 patients were collected from urinary calculi. They found that compared with patients without hair loss, the risk of urolithiasis increased by 1.3-fold in patients with vertex pattern alopecia, whereas the risk of total alopecia increased by 2.1-fold [77]. WenChieh Chen et al. showed that a larger prostate was associated with a higher prevalence of AGA, but not with its severity [75]. Naglaa F Agamia also conducted related studies (including 300 patients diagnosed with AGA and 100 controls). They found that there was a significant increase in patients with AGA meeting the diagnostic criteria for BPH (36 vs. 6.8%) than those of the control group. BPH is an important pathogenic factor associated with AGA [78]. In contrast to the above studies, the other two studies did not find any correlation between AGA and prostate volume [79, 80]. Therefore, the correlation between BPH and AGA still requires high-quality research.
Nutritional States
Evidently, nutritional deficiencies are a common cause of AGA. Ching-Huang Lai et al. investigated the concentration of heavy metals in patients with AGA, and the results showed that the concentrations of blood lead, copper, cadmium, and zinc were lower in individuals with moderate-to-severe AGA, while urine levels of lead, cadmium, and zinc in patients with AGA were higher than those in the controls. This study found for the first time that there was a significant correlation between blood vanadium concentration and the prevention of moderate-to-severe AGA [81]. Amirnia Mehdi et al. assessed the zinc and copper content in the hair of patients with AGA and alopecia areata (AA) (27 patients with AGA and 27 patients with AA; the control group comprised 27 age- and sex-matched healthy control participants). The results showed that the average hair zinc levels of patients with AA, AGA, and the control group were 98.33, 105.35, and 129.52 μg/dl, respectively, which correlated with the previous study. The average levels of copper in the hair of participants in the study and control groups were 7.91, 7.25, and 10.34, respectively. The levels of hair and serum zinc and copper in patients with AA and AGA were significantly lower than those in the control group (P < 0.05) [82]. Dinesh Gowda proposed that hair loss is not only related to the lack of trace elements but also the lack of amino acids. His results showed that histidine deficiency was observed in > 90% of AGA, leucine deficiency in 100% of participants with FPHL, alanine deficiency in 91.67% of FPHL and 91.18% of male pattern hair loss (MPHL), cysteine deficiency in 55.58% of participants with MPHL, zinc deficiency in 11.76% of participants with MPHL, copper deficiency in 29.41% of MPHL participants, and low transferrin saturation and ferritin levels in patients with FPHL [83]. Kondrakhina and Irina used direct colorimetry or atomic absorption spectroscopy to estimate the plasma element content (magnesium, calcium, zinc, copper, selenium, iron) and vitamin status (B12, D, E, and folic acid) in patients with AGA. The data revealed that compared with healthy controls, patients with AGA had a 21.4% reduction in zinc content (P = 0.003), 42.1% reduction in copper (P < 0.001), 10% reduction in magnesium (P = 0.005), and 30% reduction in selenium (P = 0.002), vitamin B12 decreased by 15.5% (P = 0.012), while vitamin D increased by 53.3% (P < 0.001). However, none of these micronutrients are related to the severity of hair loss. In contrast to previous studies, another study did not find any iron or ferritin deficiency in patients with AGA [84]. The analysis of single-nucleotide polymorphism profiles found that compared with healthy controls, patients with AGA had elevated levels of dihydrotestosterone, 17-OH-progesterone, insulin, magnesium, copper, zinc, selenium, vitamins D and E, and folic acid [85]. Another study also found that testosterone deficiency was more frequent in patients with urinary stone disease and severe AGA (P = 0.041, OR 2.38) [77]. These studies showed that nutritional deficiency or sufficiency are associated with AGA, which may provide a novel avenue for the treatment of AGA with drugs. In addition to medication, monitoring micronutrient levels before treatment may also be a necessary step.
Genetic Polymorphism
Genetic polymorphism, cigarette smoking, drinking, eating habits, sleep, infection with SARS-CoV-2 (COVID-19), infection, Cancer and metabolic diseases are high risk factors for AGA (Table2). Genetic polymorphism has become a research hotspot in AGA. Currently, researchers have identified androgen receptor (AR), 7p21, 20P11, and 2Q35 susceptibility genes on the X chromosome and other susceptibility genes that contribute to the development of male androgenetic alopecia (MAGA). The concomitant familial cases of FPHL and MAGA suggest that FPHL and MAGA share a common genetic background [86], but these study samples were mostly European populations. Myung Hwa Kim et al. further justified genetic susceptibility genes of AGA high-risk individuals in Asian populations [87].
Human Behaviors
The role of cigarette smoking in hair loss has become a topic of great interest to scientists. Studies have found that smoking affects female pattern baldness by causing women to have relatively low estrogen levels through aromatase inhibition and hydroxylation of estradiol. Most studies have found a positive association between cigarette smoking and hair loss, especially in AGA. However, a case–control study found that smokers were less likely to develop AGA than non-smokers. This provides an alternative explanation for the link between previous smoking and hair loss: an increased risk of smoking due to AGA [57, 88,89,90]. A cross-sectional study evaluating the effect of cigarette smoking on early onset AGA found that the prevalence of AGA was statistically higher in smokers than in non-smokers, but there was no significant association between hair loss severity and smoking intensity [91].
Quality of life also has an important impact on hair loss. A cross-sectional study identified that stressful environments related to urban living standards and anxiety about hair loss are key triggers for AGA progression [3]. A study by Atallah et al. reported that the prevalence of female pattern baldness in urban areas was significantly lower than in rural areas, and there was no significant correlation with parental education and family income [92]. Liamsombut Somprasong et al. found an increased risk of sleep disturbances in AGA patients [93]. Another study also found a significant association between sleep disturbances (going to bed late or having poor sleep quality) and increased AGA severity [94].
People's dietary habits also affect AGA. Yanhua Yi et al. found that alcohol intake increased the severity of female pattern baldness [95]. Agaoglu et al. believe that red meat consumption and insufficient intake of fruits and vegetables are risk factors for early onset AGA in young men [96].
COVID-19
Androgen signaling plays a central role in AGA etiology and has been shown to be associated with severe COVID-19 symptoms in men. There is a biological link between these traits [98]. In Dunja Veskovic's observational study, AGA severity was associated with poor prognosis of COVID-19 [99]. Wambier et al. noted that COVID-19-positive patients have a higher prevalence of AGA compared with the general population of the same age [100]. Meta-analysis by Betty Nguyen suggested that AGA may be a risk factor for severe COVID-19 [101]. Among hospitalized patients with COVID-19, males have a significantly higher incidence and severity of AGA than females, and have a worse prognosis. The study also found a significant association between the severity of AGA and adverse outcomes in men compared with women [102]. In contrast, Moein Baghani et al. found that the severity of COVID-19 in hospitalized patients was not associated with the severity of AGA [97].
Other Illnesses
In addition to the role of androgens in AGA development, scalp inflammation can exacerbate AGA development. Bhoyrul Bevin confirmed that AGA was accompanied by seborrheic dermatitis (SD) using microscopic examination of hair [103]. Sevil Alan examined the clinical and laboratory signs of 141 women with acne vulgaris and 73 healthy women and found that the incidence of AGA and HA in the acne group was significantly higher than that in the control group [104]. Another case–control study also found that the prevalence of AGA was significantly higher in the acne group than in the control group. This study did not find an association between serum androgen levels and acne [105]. These studies suggest that acne and AGA may be independently related, and it was not previously thought that hyperandrogenism plays a role in it. However, current research on this topic is still limited. Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease that causes multiple system involvement [106]. Early AGA (P = 0.01) was more common in patients with DM1 than in controls and was higher in men (P < 0.0001) [107]. Colombia surveyed 330 students and found that 84% of them with autoimmune diseases had alopecia [108]. Another study of 67 young men with autoimmune thyroiditis found that 37% of them had early onset AGA [109]. These studies have indicated that AGA is a complication of most diseases.
Conclusions
This review summarizes the pathological factors of AGA, including endocrine disease, cancer, mental disease, metabolic disease, cardiovascular diseases, urinary system diseases, nutritional states, genetic polymorphism, social and daily behaviors and infection with COVID-19, indicating that AGA may be a complication and manifestation of underlying systemic diseases. Clear causes of AGA may be important for obtaining the correct treatment. For secondary AGA, it is critical to treat the primary disease, which is important to improve AGA. However, the relationship between AGA and other diseases remains unclear. Therefore, uncovering the potential mechanisms would provide a new therapeutic target for AGA. In summary, dermatologists and patients need to increase the potential risk of AGA-related comorbidities. This may play an important role in the occurrence and development of AGA. Similarly, AGA may also be one of the manifestations of underlying systemic diseases.
References
Cash TF. The psychosocial consequences of androgenetic alopecia: a review of the research literature. Br J Dermatol. 1999;141(3):398–405.
Rajabi F, Drake LA, Senna MM, Rezaei N. Alopecia areata: a review of disease pathogenesis. Br J Dermatol. 2018;179:1033–48.
Elsaie LT, Elshahid AR, Hasan HM, et al. Cross sectional quality of life assessment in patients with androgenetic alopecia. Dermatol Ther. 2020;33(4): e13799.
Sorbellini E, Pinto D, Marzani B, Rinaldi F. Drug treatment for androgenetic alopecia: first Italian questionnaire survey on what dermatologists think about finasteride. Dermatol Ther. 2018;8:259–67.
Girijala RL, Riahi RR, Cohen PR. Platelet-rich plasma for androgenic alopecia treatment: a comprehensive review. Dermatol Online J. 2018;24(7):13030.
Kubanovl AA, Gallyamova YA, Korableva OA. The study of growth factors in patients with androgenic alopecia. Biomed Pharmacol J. 2017;10:1219–28.
Schweiger ES, Boychenko O, Bernstein RM. Update on the pathogenesis, genetics and medical treatment of patterned hair loss. J Drugs Dermatol. 2010;9:1412–9.
Lolli F, Pallotti F, Rossi A, Fortuna MC, Caro G, Lenzi A, et al. Androgenetic alopecia: a review. Endocrine. 2017;57:9–17.
English RS. A hypothetical pathogenesis model for androgenic alopecia: clarifying the dihydrotestosterone paradox and rate-limiting recovery factors. Med Hypotheses. 2018;111:73–81.
Sasaki M, Shinozaki S, Shimokado K. Sulforaphane promotes murine hair growth by accelerating the degradation of dihydrotestosterone. Biochem Biophys Res Commun. 2016;472:250–4.
Motofei IG, Rowland DL, Tampa M, Sarbu MI, Mitran MI, Mitran CI, et al. Finasteride and androgenic alopecia; from therapeutic options to medical implications. J Dermatolog Treat. 2020;31:415–21.
Gupta AK, Talukder M, Venkataraman M, Bamimore MA. Minoxidil: a comprehensive review. J Dermatol Treat. 2021;20:1–11.
Casanova MF, Frye RE, Gillberg C, Casanova EL. Editorial: comorbidity and autism spectrum disorder. Front Psych. 2020;11: 617395.
Bo-Kyung KSJC, Hee-Chul C, Sung-Soo O, Won-Soo L. Gender-specific risk factors for androgenetic alopecia in the Korean general population: associations with medical comorbidities and general health behaviors. Int J Dermatol. 2018;57(2):183–92.
Chung HC, Choe SJ, Lee S, Oh SS, Lee WS. Medical comorbidities and the onset of androgenetic alopecia: a population-based, case-control study. Ann Dermatol. 2018;30:251–2.
Descamps V, Mahe E, Maccari F, Begon E, Barthelemy H, Reguiai Z, et al. Severe androgenetic alopecia as a proxy of metabolic syndrome in male psoriatic patients older than 59 years. Eur J Dermatol. 2014;24:356–60.
Juliano VSCFR, Fernanda HddS, Elisa BDS, Fernanda RLB. Hair loss perception and symptoms of depression in female outpatients attending a general dermatology clinic. An Bras Dermatol. 2012;87(3):412–7.
Lee S, Lee H, Lee CH, Lee WS. Comorbidities in alopecia areata: a systematic review and meta-analysis. J Am Acad Dermatol. 2019;80:466-477.e416.
Conic RZ, Tamashunas NL, Damiani G, Fabbrocini G, Cantelli M, Bergfeld WF. Comorbidities in pediatric alopecia areata. J Eur Acad Dermatol Venereol. 2020;34:2898–901.
Egeberg A, Anderson S, Edson-Heredia E, Burge R. Comorbidities of alopecia areata: a population-based cohort study. Clin Exp Dermatol. 2021;46:651–6.
Vinay K, Sawatkar GU, Dogra S. Hair manifestations of endocrine diseases: a brief review. Indian J Dermatol Venereol Leprol. 2018;84:528–38.
Yildiz BO. Diagnosis of hyperandrogenism: clinical criteria. Best Pract Res Clin Endocrinol Metab. 2006;20:167–76.
Gambineri A, Trimarchi F. Endo&Art why Diana is depicted with mild androgenic alopecia? J Endocrinol Invest. 2021;45(1):229–30.
Clark CM, Rudolph J, Gerber DA, Glick S, Shalita AR, Lowenstein EJ. Dermatologic manifestation of hyperandrogenism: a retrospective chart review. Skinmed. 2014;12:84–8.
Guarino A, Di Benedetto L, Giovanale V, Vinciguerra GLR, Stoppacciaro A, Bellati F, et al. Hyperandrogenism in a postmenopausal woman: a rare case of ectopic adrenal cortical gland. Gynecol Endocrinol. 2017;33:185–7.
Roth TM. Postmenopausal ovarian hyperthecosis associated with rapid testosterone excess. J Gynecol Surg. 2018;34:36–9.
Özdemir S, Özdemir M, Gorkemli H, Kiyici A, Bodur S. Specific dermatologic features of the polycystic ovary syndrome and its association with biochemical markers of the metabolic syndrome and hyperandrogenism. 2010;89:199–204.
Feng JG, Guo Y, Ma LA, Xing J, Sun RF, Zhu W. Prevalence of dermatologic manifestations and metabolic biomarkers in women with polycystic ovary syndrome in north China. J Cosmet Dermatol. 2018;17:511–7.
Quinn M, Shinkai K, Pasch L, Kuzmich L, Cedars M, Huddleston H. Prevalence of androgenic alopecia in patients with polycystic ovary syndrome and characterization of associated clinical and biochemical features. Fertil Steril. 2014;101:1129–34.
Filatova VA, Rozhivanov RV. Features of hyperandrogenism in men. Problemy Endokrinologii. 2021;67:111–5.
Belenkaya LV, Ivanov OV, Panarina OV, Rashidova MA, Sholokhov LF. Trichology features of alopecia in reproductive age women with polycystic ovary syndrome. Acta Biomedica Scientifica (East Siberian Biomed J). 2017;2:9–14.
Jalilian A, Kiani F, Sayehmiri F, Sayehmiri K, Khodaee Z, Akbari M. Prevalence of polycystic ovary syndrome and its associated complications in Iranian women: a meta-analysis. Iran J Reprod Med. 2015;13:591–604.
Cooper HE, Spellacy WN, Prem KA, Cohen WD. Hereditary factors in the Stein-Leventhal syndrome. Am J Obstet Gynecol. 1968;100:371–87.
Sanke S, Chander R, Jain A, Garg T, Yadav P. A comparison of the hormonal profile of early androgenetic alopecia in men with the phenotypic equivalent of polycystic ovarian syndrome in women. JAMA Dermatol. 2016;152:986–91.
Tu YA, Lin SJ, Chen PL, Chou CH, Huang CC, Ho HN, et al. HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome. J Formos Med Assoc. 2019;118:1225–31.
Schmidt TH, Khanijow K, Cedars MI, Huddleston H, Pasch L, Wang ET, et al. Cutaneous findings and systemic associations in women with polycystic ovary syndrome. JAMA Dermatol. 2016;152:391–8.
Rodríguez-Gutiérrez R, Salcido-Montenegro A, González-González JG. Early clinical expressions of insulin resistance: the real enemy to look for. Diabetes Ther. 2018;9:435–8.
Gatherwright J, Liu MT, Gliniak C, Totonchi A, Guyuron B. The contribution of endogenous and exogenous factors to female alopecia: a study of identical twins. Plast Reconstr Surg. 2012;130:1219–26.
Adibi N, Robati RM. Skin and metabolic syndrome: a review of the possible associations. J Res Med Sci. 2021;26:16.
Su L-H, Chen L-S, Lin S-C, Chen H-H. Association of androgenetic alopecia with mortality from diabetes mellitus and heart disease. JAMA Dermatol. 2013;149:601.
Jafari F, Nilforooshzade MA, Porajam S, Beni MH. Comparison of androgenic alopecia distribution among type 2 diabetes and healthy women in Isfahan city: a brief report. Tehran Univ Med J. 2014;72.
Schmidt JB, Lindmaier A, Spona J. Hyperprolactinemia and hypophyseal hypothyroidism as cofactors in hirsutism and androgen-induced alopecia in women. Hautarzt. 1991;42:168–72.
Schmidt JB. Hormonal basis of male and female androgenic alopecia: clinical relevance. Skin Pharmacol. 1994;7:61–6.
Siah TW, Muir-Green L, Shapiro J. Female pattern hair loss: a retrospective study in a tertiary referral center. Int J Trichol. 2016;8:57–61.
Babaei K, Kavoussi H, Rezaei M, Kavoussi R. Characteristics of telogen effluvium in COVID-19 in western Iran (2020). An Bras Dermatol. 2021;96:688–92.
Liang WJ, Song LY, Peng Z, Zou Y, Dai SM. Possible association between androgenic alopecia and risk of prostate cancer and testicular germ cell tumor: a systematic review and meta-analysis. BMC Cancer. 2018;18:11.
Rokni GR, Gorji AMH, Sharifian M, Talarposhti AHR, Barzgarnejad A. The relationship between androgenic alopecia and prostate cancer. Int J Med Res Health Sci. 2016;5:23–9.
Khaled HN, Allah AMA, Abdelhameed AA, Shehata WA. Role of serum androgens and prostate-specific antigen levels in men with androgenetic alopecia. Egypt J Dermat Vener. 2020;40:106–11.
Wesolowska A, Tuszynska A, Szlendak-Sauer K, Smolarczyk R, Grabowska-Derlatka L, Przytula E. Ovarian Leydig cell tumour in a postmenopausal woman with alopecia. Eur J Gynaecol Oncol. 2019;40:154–6.
Sun LM, Lin MC, Muo CH, Liang JA, Sung FC, Kao CH. Women with alopecia exhibit a higher risk for thyroid cancer: a nationwide cohort study. J Dermatol Sci. 2014;74:18–22.
Ferrinho C, Silva E, Oliveira M, Duarte JS. Ovarian Leydig cell tumor and postmenopausal hirsutism with signs of virilisation. BMJ Case Rep. 2021;14:4.
Catalona WJ. Prostate cancer screening. Med Clin N Am. 2018;102:199–214.
Memon FH, Rahimoon AG, Kumar P, Memon SH, Siddiqui E, Devrajani T, et al. Androgenetic alopecia as a marker of metabolic syndrome. J Pharm Res Int. 2021;33:146–53.
Dharam Kumar KC, Kishan Kumar YH, Neladimmanahally V. Association of androgenetic alopecia with metabolic syndrome: a case-control study on 100 patients in a tertiary care hospital in South India. Indian J Endocrinol Metab. 2018;22:196–9.
Gopinath H, Upadya GM. Metabolic syndrome in androgenic alopecia. Indian J Dermatol Venereol Leprol. 2016;82:404–8.
Behrangi E, Azizian Z, Ardestani FS, Najafi Z, Vakili SH. Association of androgenic alopecia with metabolic syndrome. Ann Med Health Sci Res. 2018;8:91–3.
Vora RV, Kota R, Singhal RR, Anjaneyan G. Clinical profile of androgenic alopecia and its association with cardiovascular risk factors. Indian J Dermatol. 2019;64:19–22.
Bakry OA, Shoeib MA, El Shafiee MK, Hassan A. Androgenetic alopecia, metabolic syndrome, and insulin resistance: is there any association? A case-control study. Indian Dermatol Online J. 2014;5:276–81.
Goradel NH, Hour FG, Negahdari B, Malekshahi ZV, Hashemzehi M, Masoudifar A, et al. Stem cell therapy: a new therapeutic option for cardiovascular diseases. J Cell Biochem. 2018;119:95–104.
Mohammed S, Ola B, Shimaa S, Amira I. Troponin I in alopecia areata and female pattern hair loss. Menoufia Medical Journal. 2021;34:498.
Amamoto M, Yamada T, Hara K. Updated meta-analysis of the relation between heart disease and androgenic alopecia or alopecia areata. Australas Med J. 2018;11:25–33.
Arias-Santiago S, Gutiérrez-Salmerón MT, Castellote-Caballero L, Buendía-Eisman A, Naranjo-Sintes R. Androgenetic alopecia and cardiovascular risk factors in men and women: a comparative study. J Am Acad Dermatol. 2010;63:420–9.
Wang YX, Chen XW, Wang SB, Gu LF, Li YF, Ma Y, et al. Association between androgenic alopecia and coronary artery disease: a cross-sectional study of Han Chinese male population. Int J Gen Med. 2021;14:4809–18.
Kim MW, Shin IS, Yoon HS, et al. Lipid profile in patients with androgenetic alopecia: a meta-analysis. J Eur Acad Dermatol Venereol JEADV. 2017;31(6):942–51.
Sharma K, Humane D, Shah K, Patil S, Charaniya R, Meniya J. Androgenic alopecia, premature graying, and hair thinning as independent predictors of coronary artery disease in young Asian males. Cardiovasc Endocrinol. 2017;6:152–8.
Ahouansou S, Le Toumelin P, Crickx B, Descamps V. Association of androgenetic alopecia and hypertension. Eur J Dermatol. 2007;17:220–2.
El EF, Ei RS. Androgenetic alopecia as an early marker for hypertension. Egypt J Dermatol Venerol. 2013;33:63.
Arias SS, Gutierrez SMT, Buendia EA, Giron PMS, Naranjo SR. Hypertension and aldosterone levels in women with early-onset androgenetic alopecia. Br J Dermatol. 2010;162(4):786–9.
Danesh-Shakiba M, Poorolajal J, Alirezaei P. Androgenetic alopecia: relationship to anthropometric indices, blood pressure and life-style habits. Clin Cosmet Investig Dermatol. 2020;13:137–43.
Wang X, Xiong CP, Zhang L, Yang B, Wei RF, Cui LQ, et al. Psychological assessment in 355 Chinese college students with androgenetic alopecia. Medicine. 2018;97:4.
ChunHsien H, Yun F, ChingChi C. Health-related quality of life, depression, and self-esteem in patients with androgenetic alopecia: a systematic review and meta-analysis. JAMA Dermatol. 2021;157(8):963–70.
Tas B, Kulacaoglu F, Belli H, Altuntas M. The tendency towards the development of psychosexual disorders in androgenetic alopecia according to the different stages of hair loss: a cross-sectional study. An Bras Dermatol. 2018;93:185–90.
Tabolli S, Sampogna F, di Pietro C, Mannooranparampil TJ, Ribuffo M, Abeni D. Health status, coping strategies, and alexithymia in subjects with androgenetic alopecia: a questionnaire study. Am J Clin Dermatol. 2013;14:139–45.
Wu BY, Wu BJ, Lee SM, Sun HJ, Chang YT, Lin MW. Prevalence and associated factors of comorbid skin diseases in patients with schizophrenia: a clinical survey and national health database study. Gen Hosp Psychiatry. 2014;36:415–21.
Chen WC, Yang CC, Chen GY, Wu MC, Sheu HM, Tzai TS. Patients with a large prostate show a higher prevalence of androgenetic alopecia. Arch Dermatol Res. 2004;296:245–9.
Kucerova R, Bienova M, Kral M, Bouchal J, Trtkova KS, Burdova A, et al. Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer. J Eur Acad Dermatol Venereol. 2015;29:91–6.
Polat EC, Ozcan L, Otunctemur A, Ozbek E. Relation of urinary stone disease with androgenetic alopecia and serum testosterone levels. Urolithiasis. 2016;44:409–13.
Agamia NF, Abou Youssif T, El-Hadidy A, El-Abd A. Benign prostatic hyperplasia, metabolic syndrome and androgenic alopecia: is there a possible relationship? Arab J Urol. 2016;14:157–62.
Aourag N, Langenhuijsen JF, d’Ancona F, Heesakkers J. Can we predict prostate size by scoring baldness? The relationship of androgenic alopecia and lower urinary tract symptoms. Central Eur J Urol. 2019;72:39–43.
Dastgheib L, Shirazi M, Moezzi I, Dehghan S, Sadati MS. Is there a relationship between androgenic alopecia and benign prostatic hyperplasia? Acta Med Iran. 2015;53:30–2.
Lai CH, Chu NF, Chang CW, Wang SL, Yang HC, Chu CM, et al. Androgenic alopecia is associated with less dietary soy, higher blood vanadium and rs1160312 1 polymorphism in Taiwanese communities. PLoS ONE. 2013;8:11.
Amirnia M, Sinafar S, Sinafar H, Nuri M, Sadeghi AT. Assessment of zinc and copper contents in the hair and serum and also superoxide dismutase, glutathion peroxidase and malondi aldehyde in serum in androgenetic alopecia and alopecia areata. Life Sci J. 2013;10:204–9.
Gowda D, Premalatha V, Imtiyaz DB. Prevalence of nutritional deficiencies in hair loss among Indian participants: results of a cross-sectional study. Int J Trichol. 2017;9:101–4.
Kondrakhina IN, Verbenko DA, Zatevalov AM, Gatiatulina ER, Nikonorov AA, Deryabin DG, et al. A cross-sectional study of plasma trace elements and vitamins content in androgenetic alopecia in men. Biol Trace Elem Res. 2021;199:3232–41.
Kondrakhina IN, Verbenko DA, Zatevalov AM, Kubanov AA, Deryabin DG. The value of genetic and non-genetic factors in the emergence and in the development of androgenetic alopecia in men: multifactor analysis. Ann Russian Acad Med Sci. 2019;74:167–75.
Liang B, Ding Y, Zhou Y, et al. Evaluation of susceptibility genes/loci associated with male androgenetic alopecia (MAGA) for female-pattern hair loss in a Chinese Han population and a brief literature review. Med Sci Monitor Int Med J Exp Clin Res. 2021;27: e933424.
Kim IY, Kim JH, Choi JE, et al. The first broad replication study of SNPs and a pilot genome-wide association study for androgenetic alopecia in Asian populations. J Cosmet Dermatol. 2022. https://doi.org/10.1111/jocd.15187.
Babadjounia A, Pouldar FD, Hedayati B, et al. The effects of smoking on hair health: a systematic review. Skin Appendage Disord. 2021;7(4):251–64.
Severi G, Sinclair R, Hopper JL, et al. Androgenetic alopecia in men aged 40–69 years: prevalence and risk factors. Br J Dermatol. 2003;149(6):1207–13.
Fortes C, Mastroeni S, Mannooranparampil TJ, et al. The combination of overweight and smoking increases the severity of androgenetic alopecia. Int J Dermatol. 2017;56(8):862–7.
Salem AS, Ibrahim HS, Abdelaziz HH, et al. Implications of cigarette smoking on early-onset androgenetic alopecia: a cross-sectional Study. J Cosmet Dermatol. 2021;20(4):1318–24.
Youssef SME, Atallah RB, Zaky MS, et al. Urban-rural differences in the prevalence of female pattern hair loss among secondary school girls: a cross-sectional study. J Cosmet Dermatol. 2022;21(5):2229–35.
Liamsombut S, Pomsoong C, Kositkuljorn C, et al. Sleep quality in men with androgenetic alopecia. Sleep Breath. 2022. https://doi.org/10.1007/s11325-022-02618-x.
Yi Y, Qiu J, Jia J, et al. Severity of androgenetic alopecia associated with poor sleeping habits and carnivorous eating and junk food consumption-A web-based investigation of male pattern hair loss in China. Dermatol Ther. 2020;33(2): e13273.
Agaoglu E, Kaya EH, Acer E, et al. Prevalence of early-onset androgenetic alopecia and its relationship with lifestyle and dietary habits. Italian J Dermatol Venereol. 2021;156(6):675–80.
Yi Y, Li X, Jia J, et al. Effect of behavioral factors on severity of female pattern hair loss: an ordinal logistic regression analysis. Int J Med Sci. 2020;17(11):1584–8.
Henne SK, Hochfeld LM, Maj C, et al. Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID-19. Skin Health Dis. 2021;1(4): e72.
Veskovic D, Ros T, Icin T, et al. Association of androgenetic alopecia with a more severe form of COVID-19 infection. Ir J Med Sci. 2022. https://doi.org/10.1007/s11845-022-02981-4.
Wambier CG, Vano GS, Mccoy J, et al. Androgenetic alopecia present in the majority of patients hospitalized with COVID-19: the “Gabrin sign.” J Am Acad Dermatol. 2020;83(2):680–2.
Nguyen B, Tosti A. Alopecia in patients with COVID-19: A systematic review and meta-analysis. JAAD Int. 2022;7:67–77.
Ghafoor R, Ali SM, Patil A, et al. Association of androgenetic alopecia and severity of coronavirus disease 2019. J Cosmet Dermatol. 2022;21(3):874–9.
Baghani M, Pourani MR, Nekooghadam SM, et al. Androgenetic alopecia and COVID-19: Is there a clinical connection? J Cosmet Dermatol. 2022;21(2):420–5.
Bevin B. A simple technique to distinguish fibrosing alopecia in a pattern distribution from androgenetic alopecia and concomitant seborrheic dermatitis. J Am Acad Dermatol. 2021;86(1):163–5.
Alan S, Cenesizoglu E. Effects of hyperandrogenism and high body mass index on acne severity in women. Saudi Med J. 2014;35:886–9.
Khezrian L, Yazdanfar A, Azizian Z, Hassani P, Feyzian M. The relationship between acne and other hyperandrogenism signs. J Skin Stem Cell. 2016. https://doi.org/10.5812/jssc.64187.
Portaro S, Naro A, Guarneri C, Di Toro G, Manuli A, Calabrò RS. Hemangiomas of the tongue and the oral cavity in a myotonic dystrophy type 1 patient: a case report. Medicine (Baltimore). 2018;97: e13448.
Campanati A, Giannoni M, Buratti L, Cagnetti C, Giuliodori K, Ganzetti G, et al. Skin features in myotonic dystrophy type 1: an observational study. Neuromuscular Disord NMD. 2015;25:409–13.
Castrillon JJC, Garcia MCB, Reyn FJB, Valbuena SMG, Urrego LYM, Diaz DAP. Study on hair loss and care practices among students of the Universidad de Manizales, Manizales (Colombia), 2016. Arch Med. 2019;19:18.
Krysiak R, Kowalcze K, Okopien B. The impact of exogenous vitamin D on thyroid autoimmunity in euthyroid men with autoimmune thyroiditis and early-onset androgenic alopecia. Pharmacol Rep. 2021;73:1439–47.
Acknowledgements
Funding
This study and the Rapid Service Fee were funded by Yong Zhang.
Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Author contributions
All authors contributed to the study conception and design. Modifications were performed by Guoqiong Zhang and Yong Zhang. The first draft of the manuscript in English was written by Shuang Chen and Xiaohang Xie. All authors read and approved the final manuscript.
Disclosures
Shuang Chen, Xiaohang Xie, Guoqiong Zhang, and Yong Zhang have nothing to disclose.
Compliance with ethics guidelines
This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.
Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
About this article
Cite this article
Chen, S., Xie, X., Zhang, G. et al. Comorbidities in Androgenetic Alopecia: A Comprehensive Review. Dermatol Ther (Heidelb) 12, 2233–2247 (2022). https://doi.org/10.1007/s13555-022-00799-7
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13555-022-00799-7